{"title":"Antitumor Agents for Research","description":"\u003cp\u003e\u003cstrong\u003eAntitumor Agents for Research\u003c\/strong\u003e — menghimpun senyawa yang berperan sebagai model eksperimen dan senyawa acuan pada riset biologi kanker, mencakup molekul kecil dengan target mekanisme seluler tertentu seperti pembelahan sel, siklus sel, atau jalur sinyal terkait pertumbuhan sel.\u003c\/p\u003e\u003cp\u003eAntitumor Agents for Research ini dipakai peneliti biologi kanker dan farmakologi sebagai bahan uji in vitro pada kultur sel, untuk mempelajari mekanisme penghambatan proliferasi, induksi apoptosis, atau interaksi dengan target protein tertentu. Senyawa dalam kategori ini juga berfungsi sebagai kontrol positif pada uji skrining, standar pembanding pada pengembangan senyawa baru, serta model struktur untuk studi hubungan struktur-aktivitas di laboratorium riset kanker.\u003c\/p\u003e\u003cp\u003eContoh produk dalam koleksi ini: \u003ca href=\"\/en\/products\/tci2510c230217033\"\u003eTCI C2302 458-37-7 Curcumin (Synthetic)\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510b552012169\"\u003eTCI B5520 714971-09-2 BMS-599626\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510c031414369\"\u003eTCI C0314 67-97-0 Cholecalciferol\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510b570012413\"\u003eTCI B5700 10309-37-2 Bakuchiol\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510a0410592\"\u003eTCI A0410 54-62-6 Aminopterin\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510b577512514\"\u003eTCI B5775 848695-25-0 BIIB 021\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510i082236099\"\u003eTCI I0822 961-29-5 Isoliquiritigenin\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510b577612516\"\u003eTCI B5776 356559-20-1 SB-525334\u003c\/a\u003e.\u003c\/p\u003e\u003cp\u003ePerhatikan kemurnian analitik, kelarutan dalam pelarut uji (misalnya DMSO), serta stabilitas senyawa selama penyimpanan agar hasil uji in vitro tetap konsisten dan dapat direproduksi pada berbagai ulangan percobaan. Seluruh produk merupakan produk asli Tokyo Chemical Industry (TCI) Jepang, dengan kemurnian, kemasan, dan kondisi penyimpanan tercantum pada halaman masing-masing item.\u003c\/p\u003e\u003cp\u003eKategori lain yang sejajar di bawah Cancer Research, sering dipakai bersamaan dalam satu alur kerja laboratorium:\u003c\/p\u003e\u003cul\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l4-chemopreventive-agents-cancer-research\"\u003eChemopreventive Agents [Cancer Research]\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l4-cancer-metabolism\"\u003eCancer Metabolism\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l4-tumor-growth-regulation-cancer-research\"\u003eTumor Growth Regulation [Cancer Research]\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l4-carcinogens-cancer-research\"\u003eCarcinogens [Cancer Research]\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l4-angiogenesis-cancer-research\"\u003eAngiogenesis [Cancer Research]\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l4-cellular-analysis-cancer-research\"\u003eCellular Analysis [Cancer Research]\u003c\/a\u003e\u003c\/li\u003e\n\u003c\/ul\u003e\u003cp\u003eKembali ke \u003ca href=\"\/en\/collections\/tci-l3-cancer-research\"\u003eCancer Research\u003c\/a\u003e. Untuk pengadaan volume besar, kemasan khusus, atau grade tertentu, hubungi tim AMI Scientific — distributor resmi TCI Japan di Indonesia — untuk pengecekan ketersediaan dan lead time langsung ke Jepang.\u003c\/p\u003e","products":[{"product_id":"tci2510b552012169","title":"TCI B5520 714971-09-2 BMS-599626","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eBMS-599626 (CAS 714971-09-2) is a research-grade compound supplied by TCI, known as a selective kinase inhibitor used in laboratory studies of HER-related cell signaling pathways. It is commonly applied in oncology research, including in vitro and in vivo assays investigating tumor growth and drug resistance mechanisms. The product is available in 10 mg and 50 mg packaging for pharmaceutical and biomedical research purposes.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"10mg","offer_id":48085885026522,"sku":"TCI2510B552012169","price":3740000.0,"currency_code":"IDR","in_stock":true},{"title":"50mg","offer_id":48085885059290,"sku":"TCI2510B552012170","price":12986000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B5520.jpg?v=1771058686"},{"product_id":"tci2510b570012413","title":"TCI B5700 10309-37-2 Bakuchiol","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eBakuchiol is a naturally occurring meroterpene phenol isolated from *Psoralea corylifolia* seeds, widely employed as a reference standard in biochemical and pharmacological research. It is commonly applied in studies investigating retinol-like gene expression modulation, collagen and elastin synthesis, as well as antioxidant and anti-inflammatory activities. This compound also serves as a key material in natural cosmeceutical formulation development and antimicrobial screening assays.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"250mg","offer_id":48085897871578,"sku":"TCI2510B570012413","price":6269000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B5700.jpg?v=1768815865"},{"product_id":"tci2510b605512859","title":"TCI B6055 182498-32-4 SB 225002","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B6055 (SB 225002, CAS 182498-32-4) is a potent and selective non-peptide antagonist of the CXCR2 interleukin-8 (IL-8) receptor, widely utilized in cancer research and cell biology studies. This compound is commonly applied in investigations of tumor metastasis, angiogenesis, and inflammatory signaling pathways associated with oncogenesis. Available in 10 mg and 50 mg packaging options under the TCI brand, it is a reliable reagent for laboratories conducting advanced biomedical and pharmacological research.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"10mg","offer_id":48085917040858,"sku":"TCI2510B605512859","price":4189000.0,"currency_code":"IDR","in_stock":true},{"title":"50mg","offer_id":48085917073626,"sku":"TCI2510B605512860","price":13857000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6055.jpg?v=1768815963"},{"product_id":"tci2510b605612861","title":"TCI B6056 694433-59-5 SB-505124","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B6056 (SB-505124) is a selective inhibitor of TGF-β type I receptors (ALK4, ALK5, and ALK7), commonly used as a reference compound in TGF-β\/Smad signaling pathway studies. This compound is widely applied in cancer research to investigate tumor cell proliferation, metastasis, and epithelial-mesenchymal transition (EMT), as well as in developmental biology and stem cell research. It is available in 5 mg and 25 mg packaging variants, suitable for in vitro and cell-based assays.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5mg","offer_id":48085917139162,"sku":"TCI2510B605612861","price":2755000.0,"currency_code":"IDR","in_stock":true},{"title":"25mg","offer_id":48085917171930,"sku":"TCI2510B605612862","price":9838000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6056.jpg?v=1768815966"},{"product_id":"tci2510b644313334","title":"TCI B6443 113558-15-9 Baohuoside I","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B6443 Baohuoside I (CAS 113558-15-9) is a naturally derived prenylated flavonoid glycoside supplied strictly for research and experimental use. It is widely used as a reference compound in phytochemical profiling and in HPLC or LC-MS analysis of plant extracts. The 25 mg pack size suits analytical method development and small-scale biological studies. Store the vial tightly closed under cold, dry, light-protected conditions and allow it to reach room temperature before opening to prevent condensation.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eZhang et al. (2019). Effect of 2″-O-Rhamnosyl Icariside II, Baohuoside I and Baohuoside II in Herba Epimedii on Cytotoxicity Indices in HL-7702 and HepG2 Cells. \u003cem\u003eMolecules\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.3390\/molecules24071263\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.3390\/molecules24071263\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eMa et al. (2005). Baohuoside-1 inhibits activated T cell proliferation at G1–S phase transition. \u003cem\u003eTransplant Immunology\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1016\/j.trim.2005.05.002\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1016\/j.trim.2005.05.002\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eLin et al. (2026). Baohuoside I Combated Cryptocaryon irritans via Dual Targeting of Parasite Apoptosis and Host Defense Enhancement. \u003cem\u003eAntioxidants\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.3390\/antiox15030396\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.3390\/antiox15030396\u003c\/a\u003e\n\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003e\u003csmall\u003eReferences were compiled automatically from Crossref and every DOI was verified to exist. AMI Scientific is not affiliated with the authors or the publishers.\u003c\/small\u003e\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25mg","offer_id":48085940502746,"sku":"TCI2510B644313334","price":8180000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6443.jpg?v=1767093684"},{"product_id":"tci2510b650213405","title":"TCI B6502 321674-73-1 BIBR 1532","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B6502 BIBR 1532 (CAS 321674-73-1) is a small-molecule research compound widely used as a telomerase inhibitor in cancer biology studies. Researchers apply it in cell culture experiments to probe telomere maintenance, replicative capacity, and tumour cell proliferation. The 25 mg research pack size is convenient for preparing stock solutions and running repeated assays with consistent material. Please handle the compound with standard laboratory protective equipment and follow the storage guidance stated on the manufacturer's label and safety documentation.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eRomaniuk-Drapała et al. (2025). Telomerase inhibitors TMPyP4 and BIBR 1532 show synergistic antitumor activity in combination with chemotherapeutic drugs. \u003cem\u003eScientific Reports\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1038\/s41598-025-13496-0\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1038\/s41598-025-13496-0\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eBarma et al. (2003). Inhibition of telomerase by BIBR 1532 and related analogues. \u003cem\u003eBioorganic \u0026amp; Medicinal Chemistry Letters\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1016\/s0960-894x(03)00101-x\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1016\/s0960-894x(03)00101-x\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eHilal et al. (2011). Caloric Restriction Decreases Telomerase Activity and Enhances BIBR 1532 Inhibition Response on MDA‐MB 231 Cell Line. \u003cem\u003eThe FASEB Journal\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1096\/fasebj.25.1_supplement.915.10\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1096\/fasebj.25.1_supplement.915.10\u003c\/a\u003e\n\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003e\u003csmall\u003eReferences were compiled automatically from Crossref and every DOI was verified to exist. AMI Scientific is not affiliated with the authors or the publishers.\u003c\/small\u003e\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25mg","offer_id":48085943550170,"sku":"TCI2510B650213405","price":3852000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6502.jpg?v=1769144623"},{"product_id":"tci2510b654813475","title":"TCI B6548 33171-05-0 Bisdemethoxycurcumin","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eBisdemethoxycurcumin (CAS 33171-05-0) is one of the three principal curcuminoids found in turmeric rhizome, differing from curcumin by the absence of methoxy groups on both aromatic rings. It is commonly used as a reference compound for curcuminoid profiling by HPLC or TLC, and for in vitro bioactivity studies where a single, defined curcuminoid is preferred over a crude extract. Curcuminoids are light sensitive and degrade under alkaline conditions, so the material should be stored cool, dry, and protected from light, with working solutions prepared fresh. AMI Scientific supplies it in a 1 g pack size for research and experimental use.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eMohammadi et al. (2018). Inhibition of amyloid fibrillation of lysozyme by bisdemethoxycurcumin and diacetylbisdemethoxycurcumin. \u003cem\u003eBiophysical Chemistry\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1016\/j.bpc.2018.02.005\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1016\/j.bpc.2018.02.005\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eLappichetpaiboon (2025). Anticandidal effects of bisdemethoxycurcumin \u0026amp; melatonin with dual light emitting diode in photodynamic therapy. \u003cem\u003ePhotodiagnosis and Photodynamic Therapy\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1016\/j.pdpdt.2025.104797\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1016\/j.pdpdt.2025.104797\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eJayaprakasha et al. (2006). Antioxidant activities of curcumin, demethoxycurcumin and bisdemethoxycurcumin. \u003cem\u003eFood Chemistry\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1016\/j.foodchem.2005.06.037\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1016\/j.foodchem.2005.06.037\u003c\/a\u003e\n\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003e\u003csmall\u003eReferences were compiled automatically from Crossref and every DOI was verified to exist. AMI Scientific is not affiliated with the authors or the publishers.\u003c\/small\u003e\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48085946630362,"sku":"TCI2510B654813475","price":3289000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6548.jpg?v=1767093878"},{"product_id":"tci2510b666113624","title":"TCI B6661 301836-41-9 SB 431542 [Optimized for Cell Culture]","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B6661 is SB 431542 [Optimized for Cell Culture] (CAS 301836-41-9), a small molecule inhibitor of the TGF-β type I receptor ALK5, prepared with cell culture applications in mind. Because TGF-β signaling governs differentiation, proliferation, and epithelial–mesenchymal transition, this inhibitor is a common medium component in stem cell maintenance and organoid workflows. Researchers also use it in directed differentiation protocols and in vitro fibrosis models where controlled pathway suppression is required. AMI Scientific supplies this TCI product in a 5 mg pack size, convenient for preparing stock solutions for routine culture work.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5mg","offer_id":48085952594138,"sku":"TCI2510B666113624","price":4470000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6661.jpg?v=1768204518"},{"product_id":"tci2510c035214419","title":"TCI C0352 14371-10-9 trans-Cinnamaldehyde","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003etrans-Cinnamaldehyde (TCI C0352, CAS 14371-10-9) is a conjugated aromatic aldehyde best known as the principal aroma compound of cinnamon. In the laboratory it functions as a versatile non-heterocyclic building block, offering both a reactive carbonyl group and a conjugated double bond in a single molecule. It is commonly used as a model substrate in iminium organocatalysis, Michael additions, and heterocycle construction. AMI Scientific supplies it in 25 mL and 500 mL packs, and handling in a fume hood with appropriate personal protective equipment is strongly recommended.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eGholivand et al. (2008). Simultaneous Determination of Trans-Cinnamaldehyde and Benzaldehyde in Different Real Samples by Differential Pulse Polarography and Study of Heat Stability of Trans-Cinnamaldehyde. \u003cem\u003eAnalytical Letters\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1080\/00032710802507893\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1080\/00032710802507893\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eAli et al. (2021). Trans-Cinnamaldehyde Attenuates Enterococcus faecalis Virulence and Inhibits Biofilm Formation. \u003cem\u003eAntibiotics\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.3390\/antibiotics10060702\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.3390\/antibiotics10060702\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eSwales et al. (1996). Studies on trans-cinnamaldehyde II: Mechanisms of cytotoxicity in rat isolated hepatocytes. \u003cem\u003eToxicology in Vitro\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1016\/0887-2333(95)00105-0\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1016\/0887-2333(95)00105-0\u003c\/a\u003e\n\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003e\u003csmall\u003eReferences were compiled automatically from Crossref and every DOI was verified to exist. AMI Scientific is not affiliated with the authors or the publishers.\u003c\/small\u003e\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25mL","offer_id":48085991719130,"sku":"TCI2510C035214419","price":507000.0,"currency_code":"IDR","in_stock":true},{"title":"500mL","offer_id":48085991751898,"sku":"TCI2510C035214420","price":1659000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0352.jpg?v=1767095079"},{"product_id":"tci2510c038014467","title":"TCI C0380 64-86-8 Colchicine (contains 5% Ethyl Acetate at maximum)","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C0380 Colchicine, CAS 64-86-8, is a plant-derived alkaloid widely used as a tubulin-binding inhibitor of microtubule polymerisation. By arresting dividing cells in metaphase, it is a standard tool for chromosome preparation, cell cycle studies, and antimitotic research, and is also applied in plant polyploidy induction work. This TCI grade is specified to contain a maximum of 5% ethyl acetate as residual solvent, which should be considered when preparing solutions. The material is highly toxic, intended strictly for trained laboratory research use, and is offered by AMI Scientific in 500 mg and 5 g packs.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"500mg","offer_id":48085995094234,"sku":"TCI2510C038014467","price":1322000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48085995127002,"sku":"TCI2510C038014468","price":7534000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0380.jpg?v=1767095143"},{"product_id":"tci2510c043414550","title":"TCI C0434 458-37-7 Curcumin (Natural)","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eCurcumin (Natural) TCI C0434, with CAS number 458-37-7, is a chemical compound widely used in scientific experiments, particularly in the fields of chemistry and biology. As a natural pigment derived from the root of the turmeric plant, it serves as a valuable dye in laboratory settings. This compound is commonly used to create colorimetric solutions for various analytical processes, including color tests, compound identification, and the study of chemical and biological properties. Its presence in pure form allows researchers to precisely control concentration levels and chemical reactions, making it an essential tool in experimental research.\u003c\/p\u003e\n\u003cp\u003eCurcumin is valued for its chemical stability under certain conditions, although it is highly sensitive to light and oxidation. These properties make it a preferred choice for applications where accurate and consistent results are crucial. Its natural origin also adds to its appeal, especially in studies focused on bioactive compounds. The compound’s antioxidant properties further enhance its utility in pharmacological and nutritional research, offering researchers a versatile material for a wide range of investigations.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, curcumin is frequently used in research related to the bioactivity of natural compounds. It plays a key role in studies examining anti-inflammatory and antioxidant effects, contributing to advancements in both scientific and applied research. Its availability and reliability make it a staple in many research environments, supporting the pursuit of knowledge in various scientific disciplines.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eColorimetric analysis is a common application where curcumin is used to detect and quantify specific compounds through color changes, making it ideal for qualitative and quantitative testing.\u003c\/li\u003e\n\u003cli\u003eBioactivity studies benefit from curcumin’s natural origin and antioxidant properties, enabling researchers to investigate its effects on cellular processes and biological systems.\u003c\/li\u003e\n\u003cli\u003eChemical identification processes rely on curcumin’s distinct color properties, allowing for the visualization and analysis of compounds in solution.\u003c\/li\u003e\n\u003cli\u003ePharmacological research utilizes curcumin to explore its potential therapeutic applications, particularly in inflammation and oxidative stress-related conditions.\u003c\/li\u003e\n\u003cli\u003eNutritional studies incorporate curcumin to assess its role in dietary supplements and its impact on human health, supporting research in food science and health sciences.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 458-37-7\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Stains and Dyes (for Research and Experimental Use) \u0026gt; Basic Dyes (for Research and Experimental Use)\u003c\/li\u003e\n\u003cli\u003ePack sizes: Not specified in the provided data\u003c\/li\u003e\n\u003cli\u003ePhysical form: Not specified in the provided data\u003c\/li\u003e\n\u003cli\u003eStorage note: Must be stored in a cool, dark place to prevent degradation due to light and oxidation\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eCurcumin should be stored in a cool, dark environment to maintain its chemical integrity and prevent degradation caused by light exposure and oxidation. It is recommended to keep it in airtight containers to minimize contact with air and moisture. Due to its sensitivity, it is important to avoid prolonged exposure to heat and direct sunlight. In laboratory settings, curcumin should be handled with care to prevent contamination and ensure accurate experimental results. Proper labeling and storage conditions are essential for maintaining the quality and effectiveness of this compound in research applications.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48085998436570,"sku":"TCI2510C043414550","price":676000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48085998469338,"sku":"TCI2510C043414551","price":2840000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0434.jpg?v=1767095223"},{"product_id":"tci2510c125215732","title":"TCI C1252 51481-61-9 Cimetidine","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C1252 Cimetidine (CAS 51481-61-9) is a histamine H2-receptor antagonist supplied strictly as a pharmaceutical research reagent for experimental use. Researchers apply it in receptor pharmacology studies, in vitro gastric acid secretion models, and drug-interaction work involving cytochrome P450 enzymes. It also serves as a reference substance during the development and validation of chromatographic and spectroscopic analytical methods. AMI Scientific supplies the 25 g pack for laboratory use only; it is not intended for human or veterinary application.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eMozdarani et al. (1998). Antigenotoxic effects of cimetidine against benzene induced micronuclei in mouse bone marrow erythrocytes. \u003cem\u003eToxicology Letters\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1016\/s0378-4274(98)00138-6\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1016\/s0378-4274(98)00138-6\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eOdes et al. (2009). Effect of Cimetidine on Hepatic Vitamin D Metabolism in Humans. \u003cem\u003eDigestion\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1159\/000200333\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1159\/000200333\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003e\u0026amp;NA; (1991). Cimetidine + alginic acid improves symptoms of oesophagitis while allowing a reduced cimetidine dosage. \u003cem\u003eInpharma Weekly\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.2165\/00128413-199107980-00023\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.2165\/00128413-199107980-00023\u003c\/a\u003e\n\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003e\u003csmall\u003eReferences were compiled automatically from Crossref and every DOI was verified to exist. AMI Scientific is not affiliated with the authors or the publishers.\u003c\/small\u003e\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25g","offer_id":48086059155674,"sku":"TCI2510C125215732","price":2924000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C1252.jpg?v=1767096616"},{"product_id":"tci2510c149516076","title":"TCI C1495 7689-03-4 (S)-(+)-Camptothecin","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C1495 (S)-(+)-Camptothecin (CAS 7689-03-4) is a pentacyclic quinoline alkaloid and a well-characterised topoisomerase I inhibitor. It is catalogued as a research reagent for pharmaceutical development, particularly for antibody-drug conjugate preparation, where its scaffold underpins an important class of payloads. Laboratories also use it as a positive control in cytotoxicity assays and as a starting material for analog synthesis. Supplied in 100 mg and 1 g packs; treat as a cytotoxic compound and follow the Safety Data Sheet and institutional handling procedures.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eA et al. (2016). ANNUAL VARIATION IN CAMPTOTHECIN AND 9-METHOXY CAMPTOTHECIN ACCUMULATION AND ITS DETERMINATION IN DIFFERENT PARTS OF NOTHAPODYTES NIMMONIANA BY HPLC ANALYSIS. \u003cem\u003eBulletin of Pharmaceutical Research\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.21276\/bpr.2016.6.1.3\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.21276\/bpr.2016.6.1.3\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003e(2002). Crystal Form of A Camptothecin Derivative. \u003cem\u003eJournal of Korean Pharmaceutical Sciences\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.4333\/kps.2002.32.2.081\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.4333\/kps.2002.32.2.081\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003e(2018). Characterization of Camptothecin-induced Genomic Changes in the Camptothecin-resistant T-ALL-derived Cell Line CPT-K5. \u003cem\u003eCancer Genomics \u0026amp; Proteomics\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.21873\/cgp.20068\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.21873\/cgp.20068\u003c\/a\u003e\n\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003e\u003csmall\u003eReferences were compiled automatically from Crossref and every DOI was verified to exist. AMI Scientific is not affiliated with the authors or the publishers.\u003c\/small\u003e\u003c\/p\u003e","brand":"TCI","offers":[{"title":"100mg","offer_id":48086073573594,"sku":"TCI2510C149516076","price":760000.0,"currency_code":"IDR","in_stock":true},{"title":"1g","offer_id":48086073606362,"sku":"TCI2510C149516077","price":4414000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C1495.jpg?v=1767097022"},{"product_id":"tci2510c203516667","title":"TCI C2035 147-94-4 Cytarabine","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eCytarabine, with CAS number 147-94-4, is a widely used chemical compound in biomedical and pharmacological research. It is a nucleoside analog known for its strong antitumor activity, particularly effective against leukemia and lymphoma cells. In the laboratory, Cytarabine serves as a key reagent for cancer therapy research, drug efficacy testing, and the study of anti-cancer drug mechanisms. Its role is essential in understanding the biochemical pathways involved in tumor suppression and treatment development.\u003c\/p\u003e\n\u003cp\u003eCytarabine is chemically stable under certain conditions but is highly sensitive to UV light and oxidation. It exhibits good solubility in organic solvents such as ethanol and dimethyl sulfoxide (DMSO), making it easy to dissolve and use in various experimental protocols. Its consistent purity and quality make it a preferred choice for researchers who require reliable and reproducible results. These properties ensure that Cytarabine remains a critical component in many biochemical and pharmaceutical studies.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, Cytarabine is commonly used in cancer-related research, especially in the development of chemotherapy treatments and genetic therapy studies. It is also frequently utilized in toxicity testing and the evaluation of new potential anti-cancer compounds. Its versatility and effectiveness make it an essential tool for both academic and industrial research in the region.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eCancer Therapy Research: Cytarabine is used to study the mechanisms of action and effectiveness of anti-cancer drugs in leukemia and lymphoma treatments.\u003c\/li\u003e\n\u003cli\u003eDrug Efficacy Testing: It serves as a standard reagent for evaluating the potency and therapeutic potential of new chemotherapy agents.\u003c\/li\u003e\n\u003cli\u003eToxicity Assessment: Cytarabine is employed in toxicity studies to determine the safety profile of potential pharmaceutical compounds.\u003c\/li\u003e\n\u003cli\u003eGenetic Therapy Development: It plays a role in research focused on gene therapy and targeted treatment strategies for malignant diseases.\u003c\/li\u003e\n\u003cli\u003eAnti-Cancer Compound Evaluation: It is used to test the efficacy of novel compounds in inhibiting tumor cell growth and progression.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS Number: 147-94-4\u003c\/li\u003e\n\u003cli\u003eCategory: Life Science \u0026gt; Biochemicals and Reagents \u0026gt; Antibiotics\u003c\/li\u003e\n\u003cli\u003ePack Sizes: Available in various quantities as per standard laboratory requirements\u003c\/li\u003e\n\u003cli\u003ePhysical Form: Powder\u003c\/li\u003e\n\u003cli\u003eStorage Note: Store in a cool, dark place away from light and moisture\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eCytarabine should be stored in a cool, dark environment to prevent degradation due to UV exposure and oxidation. It is recommended to keep the compound in airtight containers to minimize moisture contact. Due to its sensitivity, it is best stored in a refrigerator at 2–8°C. When handling, researchers should use appropriate personal protective equipment, such as gloves and safety goggles, to avoid direct skin or eye contact. It is important to ensure that the compound is not exposed to heat or direct sunlight during storage or use. Proper labeling and secure storage are essential to maintain the integrity and safety of the reagent in the laboratory setting.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086097658074,"sku":"TCI2510C203516667","price":873000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086097690842,"sku":"TCI2510C203516668","price":2924000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C2035.jpg?v=1767097686"},{"product_id":"tci2510c204316678","title":"TCI C2043 41575-94-4 Carboplatin","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eCarboplatin is a chemical compound widely used in pharmacological and biochemical research. As a platinum-based compound, it exhibits significant antitumor activity and is commonly employed as a chemotherapeutic agent in cancer research. In the laboratory, it plays a crucial role in evaluating drug efficacy, testing cellular responses to treatment, and studying the mechanisms of action of antitumor compounds. Its stability and solubility in organic solvents make it a versatile reagent for various experimental applications.\u003c\/p\u003e\n\u003cp\u003eCarboplatin is preferred due to its chemical stability and solubility in solvents such as ethyl acetate and acetone. These properties allow it to be easily incorporated into a wide range of chemical and biochemical experiments. Additionally, its reactivity with proteins and DNA makes it ideal for molecular interaction studies. This reactivity is essential for understanding how antitumor agents interact with biological systems, supporting both basic and applied research.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, Carboplatin is frequently used in medical and pharmaceutical research, particularly in the development of new drugs and clinical trials. It is also integral to studies focused on cancer mechanisms and alternative treatment approaches. Its application extends to experimental models that aim to improve cancer therapies and understand disease progression.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eAntitumor Mechanism Research: Carboplatin is used to study how platinum-based compounds inhibit cancer cell growth and affect DNA structure.\u003c\/li\u003e\n\u003cli\u003eDrug Efficacy Testing: It is employed in evaluating the effectiveness of chemotherapeutic agents in vitro and in experimental models.\u003c\/li\u003e\n\u003cli\u003eMolecular Interaction Studies: Its reactivity with proteins and DNA makes it suitable for investigating molecular binding and interaction processes.\u003c\/li\u003e\n\u003cli\u003eCancer Treatment Development: Carboplatin supports research into new therapeutic strategies and alternative treatments for various cancers.\u003c\/li\u003e\n\u003cli\u003eClinical Trial Protocols: It is used in experimental settings to simulate and test the effects of chemotherapy in controlled environments.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 41575-94-4\u003c\/li\u003e\n\u003cli\u003eCategory: Life Science \u0026gt; Biochemicals and Reagents \u0026gt; Pharmaceutical Research Reagents\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per standard laboratory requirements\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from light\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eCarboplatin should be stored in a cool, dry place, away from direct light and moisture. It is recommended to use airtight containers to prevent contamination and maintain chemical integrity. Due to its reactivity, it should be handled with appropriate personal protective equipment, including gloves and safety goggles. Proper ventilation is essential when working with this compound to minimize exposure. It is important to follow standard laboratory safety protocols when handling and storing Carboplatin to ensure a safe working environment.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"100mg","offer_id":48086098149594,"sku":"TCI2510C204316678","price":2980000.0,"currency_code":"IDR","in_stock":true},{"title":"1g","offer_id":48086098182362,"sku":"TCI2510C204316679","price":13941000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C2043.jpg?v=1768193804"},{"product_id":"tci2510c223616934","title":"TCI C2236 6055-19-2 Cyclophosphamide Monohydrate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C2236 Cyclophosphamide Monohydrate is an oxazaphosphorine compound supplied in its monohydrate form, widely recognised as an alkylating agent and used as a research reagent in pharmaceutical development and in the study of drug delivery systems. The compound is a classic prodrug: the molecule only becomes active after undergoing metabolic transformation, and it is precisely this property that makes it such a valuable model in the laboratory. Researchers use it to study prodrug activation, the mechanisms of DNA damage caused by alkylating agents, and the behaviour of the active species once it has been formulated into a carrier system.\u003c\/p\u003e\n\u003cp\u003eThe properties that lead researchers to select this material begin with how thoroughly it has been documented in the scientific literature, which means experimental results can be compared against a large body of earlier references rather than interpreted in isolation. The monohydrate form yields a crystalline solid that is easier to handle and to weigh consistently than the more sensitive anhydrous form, an advantage in any workflow that depends on reproducible sample preparation. Its solubility in water simplifies the preparation of test solutions, while its prodrug character makes the compound a standard comparator in formulation research, particularly when investigators want to assess whether a given carrier system successfully alters the behaviour of the parent molecule.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories this reagent is typically found in pharmaceutical faculties, in pharmacology and biomedical research groups, and in drug delivery laboratories developing carrier systems. It supports postgraduate research projects, method development work, and comparative formulation studies where a well characterised prodrug is required as a reference point. Because its behaviour is already established in the literature, it is frequently chosen for teaching-linked research and for laboratories building experimental protocols that need to be defensible against published data.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eProdrug activation studies — the compound only becomes active after metabolic transformation, making it a reliable model for tracing how an inactive molecule is converted into its working form.\u003c\/li\u003e\n\u003cli\u003eAlkylating agent mechanism research — it is used to investigate how alkylating agents cause DNA damage, a mechanism that is extensively described in the existing scientific literature.\u003c\/li\u003e\n\u003cli\u003eDrug delivery system development — researchers formulate it into carrier systems to observe how the active species behaves once it has been incorporated into a delivery vehicle.\u003c\/li\u003e\n\u003cli\u003eFormulation comparison work — its prodrug character makes it a standard comparator for assessing whether a carrier system successfully changes the behaviour of the parent compound.\u003c\/li\u003e\n\u003cli\u003eAqueous test solution preparation — its solubility in water allows straightforward preparation of test solutions, supporting experimental designs that require consistent, easily reproduced sample handling.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 6055-19-2\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Pharmaceutical Development and Drug Discovery Research Reagents \u0026gt; Drug Delivery Systems (DDS)\u003c\/li\u003e\n\u003cli\u003ePack sizes: available in standard laboratory pack sizes; please confirm the currently listed options when ordering\u003c\/li\u003e\n\u003cli\u003ePhysical form: crystalline solid, supplied as the monohydrate\u003c\/li\u003e\n\u003cli\u003eStorage: store according to the manufacturer's instructions on the product label and safety data sheet\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eStore the container closed in a cool, dry place away from direct sunlight, moisture, and incompatible materials, following the storage conditions stated by the manufacturer on the product label and safety data sheet. Keep the material in its original tightly sealed container, or in a clean, chemically compatible and clearly labelled vessel if it is subdivided. Handle the solid in a well ventilated area or fume hood, and wear appropriate personal protective equipment including gloves, safety goggles, and a laboratory coat. Because this is a cytotoxic research reagent, avoid inhalation of dust and any contact with skin or eyes, minimise the generation of airborne particles during weighing, and restrict handling to trained personnel. Consult the safety data sheet before use, and dispose of the material and any contaminated consumables through approved chemical waste channels in accordance with institutional and local regulations.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48086113452250,"sku":"TCI2510C223616934","price":3908000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48086113485018,"sku":"TCI2510C223616935","price":13127000.0,"currency_code":"IDR","in_stock":true},{"title":"1g","offer_id":48086113517786,"sku":"TCI2604C2236100","price":1266000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C2236.jpg?v=1767097973"},{"product_id":"tci2510c230217033","title":"TCI C2302 458-37-7 Curcumin (Synthetic)","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eCurcumin (Synthetic) TCI C2302 is a chemical compound widely utilized in scientific research, particularly in the fields of biochemistry and pharmaceutical sciences. As a synthetic derivative of curcumin found naturally in turmeric, it serves as a key reagent in experimental studies aimed at understanding biological mechanisms and therapeutic potential. Its versatility makes it an essential component in laboratories conducting research on antioxidant, anti-inflammatory, and pharmacological properties of natural compounds. This compound is frequently employed in both qualitative and quantitative analyses, supporting a broad range of scientific investigations.\u003c\/p\u003e\n\u003cp\u003eCurcumin is prized for its chemical stability and solubility in organic solvents such as ethyl acetate and ethanol, which facilitates its use in various chemical reactions and analytical procedures. Its ability to react effectively with different substrates enhances its applicability in biological assays, making it a preferred choice for researchers seeking reliable and consistent results. Additionally, its high purity ensures accuracy in experiments that require precise measurements and reproducible outcomes. These properties contribute to its widespread use in both academic and industrial research settings.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, curcumin is commonly used in studies related to health, pharmacology, and nutrition. It is a favored material for investigating the bioavailability and efficacy of natural compounds, supporting research into potential therapeutic applications. Its availability and reliability make it a go-to option for scientists working on projects that require a stable and high-quality reagent. This compound plays a crucial role in advancing scientific knowledge and innovation in the region.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBiochemical Research: Curcumin is used to study antioxidant and anti-inflammatory properties due to its chemical stability and reactivity.\u003c\/li\u003e\n\u003cli\u003ePharmacological Studies: It supports research into drug development by analyzing its pharmacological effects and biological interactions.\u003c\/li\u003e\n\u003cli\u003eNutritional Analysis: Curcumin is employed in studies assessing the bioavailability and health benefits of natural compounds in food.\u003c\/li\u003e\n\u003cli\u003eSynthetic Chemistry: Its solubility in organic solvents makes it ideal for chemical synthesis and compound modification.\u003c\/li\u003e\n\u003cli\u003eAnalytical Chemistry: It is used as a reagent in chromatographic and spectroscopic analyses due to its consistent chemical behavior.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS Number: 458-37-7\u003c\/li\u003e\n\u003cli\u003eCategory: Life Science \u0026gt; Biochemicals and Reagents \u0026gt; Crude Medicine Ingredients for Research and Experimental Use\u003c\/li\u003e\n\u003cli\u003ePack Sizes: As per supplier specifications\u003c\/li\u003e\n\u003cli\u003ePhysical Form: Powder\u003c\/li\u003e\n\u003cli\u003eStorage Note: Store in a cool, dry place away from light\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eCurcumin should be stored in a cool, dry environment, away from direct sunlight and moisture to maintain its chemical stability. It is recommended to keep it in a tightly sealed container to prevent contamination and degradation. Due to its organic nature, it is best stored in glass or high-density polyethylene containers to ensure safety and purity. Avoid exposure to strong oxidizing agents or reactive substances to prevent unwanted chemical reactions. Proper labeling and storage conditions are essential to ensure its integrity and usability in laboratory settings. Always handle with care, using appropriate personal protective equipment when necessary.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48086118367450,"sku":"TCI2510C230217033","price":1266000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48086118400218,"sku":"TCI2510C230217034","price":4133000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C2302.jpg?v=1767098099"},{"product_id":"tci2510c250517279","title":"TCI C2505 481-74-3 Chrysophanic Acid","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eChrysophanic Acid is a chemical compound widely used in various chemical experiments and scientific research. As a non-heterocyclic building block, it possesses a simple molecular structure yet holds significant potential for the synthesis of complex compounds. This compound is commonly utilized as a foundational material in the development of bioactive substances, including pharmaceuticals and antioxidants. In laboratory settings, it plays a crucial role in qualitative and quantitative analysis, aiding in the identification of specific compounds within samples. Its chemical stability under certain conditions makes it a reliable and versatile material for a wide range of chemical reactions.\u003c\/p\u003e\n\u003cp\u003eChrysophanic Acid is preferred due to its chemical stability, high reactivity, and consistent quality. Its ability to remain intact without easily degrading ensures predictable results in experimental processes. The compound’s high purity and consistent quality make it a trusted choice for researchers requiring precise and reliable materials. Its reactivity allows it to participate effectively in various synthetic pathways, making it suitable for diverse chemical applications. These properties contribute to its popularity among scientists and researchers working in both academic and industrial laboratories.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, Chrysophanic Acid is commonly used in scientific research, particularly in the fields of organic chemistry and pharmacy. It supports studies related to drug development, compound synthesis, and analytical chemistry. Its availability and reliability make it a key component in many research projects, ensuring accurate and reproducible results. The compound’s role in both basic and applied research underscores its importance in the scientific community in Indonesia.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis applications benefit from Chrysophanic Acid’s reactivity and structural versatility, enabling the creation of complex molecules.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical research utilizes this compound as a building block for developing bioactive compounds and drug candidates.\u003c\/li\u003e\n\u003cli\u003eAnalytical chemistry relies on Chrysophanic Acid for identifying and quantifying specific compounds in samples due to its chemical stability.\u003c\/li\u003e\n\u003cli\u003eBioactive compound development leverages its properties to synthesize antioxidants and other therapeutic agents.\u003c\/li\u003e\n\u003cli\u003eEnvironmental studies may use Chrysophanic Acid to analyze organic pollutants and their interactions in natural samples.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 481-74-3\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Non-Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per supplier specifications\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from direct sunlight and moisture\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eChrysophanic Acid should be stored in a cool, dry environment to maintain its chemical stability and prevent degradation. It is recommended to keep it in airtight containers to avoid exposure to moisture and air, which could affect its purity. Laboratory personnel should handle the compound with care, using appropriate personal protective equipment such as gloves and safety goggles. Due to its reactivity, it should be stored separately from incompatible substances to prevent unwanted chemical reactions. Proper labeling of storage containers is essential to ensure safe handling and easy identification. Regular monitoring of storage conditions helps maintain the compound’s integrity and ensures its suitability for scientific use.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"100mg","offer_id":48086129410266,"sku":"TCI2510C250517279","price":4891000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C2505.jpg?v=1767098422"},{"product_id":"tci2510c252017305","title":"TCI C2520 117048-59-6 Combretastatin A4","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eCombretastatin A4 is a chemical compound widely utilized in life science research, particularly in biochemical and reagent applications. As a key component of the *Combretaceae* plant family, it serves as a crucial research material for experimental studies. This compound is commonly used in laboratories to investigate its biological activities, including its effects on cancer cells and antioxidant properties. Its role in scientific research is significant due to its potential therapeutic applications and its relevance in pharmacological studies.\u003c\/p\u003e\n\u003cp\u003eThe unique chemical structure of Combretastatin A4 contributes to its effectiveness in various biological assays. It exhibits potent anti-cancer properties by inhibiting the growth of malignant cells and enhancing immune responses. These characteristics make it a preferred choice for researchers aiming to explore new therapeutic targets. Additionally, its stability under different laboratory conditions ensures reliable results, making it a valuable tool in both academic and industrial research settings.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, Combretastatin A4 is frequently used by researchers in academic institutions and research centers. It is integral to studies focused on cancer and metabolic diseases, supporting the development of new drugs and treatment strategies. Its availability and consistent quality make it a reliable material for experimental work, contributing to the advancement of scientific knowledge in the region.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eCancer Research: Combretastatin A4 is used to study its anti-cancer effects on various cell lines, aiding in the development of novel therapeutic strategies.\u003c\/li\u003e\n\u003cli\u003eAntioxidant Studies: Its antioxidant properties make it suitable for experiments investigating free radical scavenging and oxidative stress reduction.\u003c\/li\u003e\n\u003cli\u003ePharmacological Investigations: The compound is employed to evaluate its potential in drug development and its interaction with biological systems.\u003c\/li\u003e\n\u003cli\u003eImmunological Research: It is used to assess its impact on immune cell function and response to pathogens.\u003c\/li\u003e\n\u003cli\u003eMetabolic Disease Studies: Combretastatin A4 is utilized to explore its role in metabolic disorders and potential therapeutic applications.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 117048-59-6\u003c\/li\u003e\n\u003cli\u003eCategory: Life Science \u0026gt; Biochemicals and Reagents \u0026gt; Crude Medicine Ingredients for Research and Experimental Use\u003c\/li\u003e\n\u003cli\u003ePack sizes: Not specified\u003c\/li\u003e\n\u003cli\u003ePhysical form: Not specified\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eCombretastatin A4 should be stored in a cool, dry, and well-ventilated area away from direct sunlight. It is recommended to keep the compound in a sealed container to prevent moisture absorption and contamination. Due to its chemical stability, it can be stored at room temperature for extended periods. Researchers should handle the compound with appropriate personal protective equipment, including gloves and safety goggles, to ensure safety during preparation and use. Proper labeling of containers is essential to avoid misidentification. In laboratory settings, it should be stored in a designated chemical storage area that complies with standard safety protocols.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"250mg","offer_id":48086130327770,"sku":"TCI2510C252017305","price":20039000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C2520.jpg?v=1767098452"},{"product_id":"tci2510c273717595","title":"TCI C2737 34157-83-0 Celastrol","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eCelastrol is a chemical compound widely used in scientific research, particularly in the fields of biochemistry and pharmacology. It serves as a key reagent in laboratory experiments aimed at exploring its biological activities, including anti-inflammatory, antitumor, and antiviral effects. This compound is essential for researchers seeking to understand the mechanisms of drug action and the body's response to various medical conditions. Its versatility makes it a valuable tool in both academic and industrial research settings.\u003c\/p\u003e\n\u003cp\u003eCelastrol is favored for its stable chemical properties and solubility in organic solvents such as ethyl acetate and ethanol. These characteristics allow it to be easily incorporated into a wide range of chemical and biochemical analyses. Additionally, its complex molecular structure enables it to interact with multiple molecular targets within the body, making it a preferred choice for pharmacological studies. The compound’s unique properties support its use in experiments requiring specific biological activities.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, Celastrol is commonly used in research focused on drug development, particularly in the study of cancer therapies and autoimmune diseases. It is also utilized in academic institutions for teaching and experimental purposes. Researchers in Indonesia rely on Celastrol to conduct experiments that require a compound with well-defined biological activity and chemical stability. Its presence in laboratory workflows underscores its importance in advancing scientific knowledge in the region.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eAnti-inflammatory Research: Celastrol is used to study its effects on inflammation, making it ideal for experiments involving inflammatory disease models.\u003c\/li\u003e\n\u003cli\u003eAntitumor Studies: Its potential as an antitumor agent supports its use in cancer research, particularly in drug discovery and mechanism studies.\u003c\/li\u003e\n\u003cli\u003eAntiviral Investigations: Celastrol’s antiviral properties make it a valuable reagent for studying viral infections and potential therapeutic applications.\u003c\/li\u003e\n\u003cli\u003ePharmacological Screening: Its complex structure and biological activity make it suitable for screening compounds with specific molecular targets.\u003c\/li\u003e\n\u003cli\u003eDrug Development Protocols: Celastrol is integrated into protocols for developing new drugs, especially in the context of autoimmune and oncological research.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 34157-83-0\u003c\/li\u003e\n\u003cli\u003eCategory: Life Science \u0026gt; Biochemicals and Reagents \u0026gt; Crude Medicine Ingredients for Research and Experimental Use\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in standard laboratory quantities\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid powder\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from light\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eCelastrol should be stored in a cool, dry place, away from direct sunlight and moisture. It is recommended to use airtight containers to prevent contamination and maintain its chemical stability. Due to its solubility in organic solvents, it should be handled in a well-ventilated area to minimize exposure. Laboratory personnel should wear appropriate personal protective equipment, such as gloves and safety goggles, when handling the compound. Proper disposal procedures should be followed to ensure compliance with safety and environmental regulations. Regular monitoring of storage conditions is essential to preserve the integrity of the compound for research use.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25mg","offer_id":48086194520282,"sku":"TCI2510C273717595","price":10344000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C2737.jpg?v=1767098713"},{"product_id":"tci2510c282617701","title":"TCI C2826 511296-88-1 Cyclic Pifithrin-alpha Hydrobromide","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C2826 511296-88-1 Cyclic Pifithrin-alpha Hydrobromide is a chemical compound widely used in cancer research to investigate the mechanisms of cancer cell growth and the inhibition of cell proliferation. As a key component in biochemical and pharmacological studies, it plays a vital role in the development and testing of anti-cancer drugs. This compound is a derivative of pifithrin-alpha, which is known to inhibit topoisomerase II, an essential enzyme in DNA replication and repair. Its application in laboratory settings is critical for understanding the molecular pathways involved in cancer progression and for evaluating potential therapeutic interventions.\u003c\/p\u003e\n\u003cp\u003eThe compound is valued for its chemical stability under specific conditions, making it a reliable reagent for various research methods. Its high purity and consistent quality ensure accurate and reproducible experimental results, which are essential in scientific research. Additionally, its versatility allows it to be used in chemical reactions, the synthesis of new compounds, and biological activity assays. These properties make it a preferred choice for researchers aiming to achieve precise and reliable outcomes in their studies.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this compound is commonly used by academic institutions and research organizations. It supports studies on cancer, drug development, and biomedical research. Its relevance in advancing cancer understanding and developing more effective therapies makes it a key material in the scientific community. Its availability and reliability contribute to the quality of research conducted in Indonesia.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eCancer cell proliferation studies benefit from this compound’s ability to inhibit topoisomerase II, aiding in the evaluation of anti-cancer drug efficacy.\u003c\/li\u003e\n\u003cli\u003eBiochemical assays utilize its stability and reactivity to assess molecular interactions and enzyme inhibition mechanisms.\u003c\/li\u003e\n\u003cli\u003eDrug development programs incorporate it to test new compounds for their potential to target cancer-related pathways.\u003c\/li\u003e\n\u003cli\u003eBiomedical research applications rely on its consistent quality for reproducible results in experimental models.\u003c\/li\u003e\n\u003cli\u003eAcademic research institutions use it to explore cancer biology and develop novel therapeutic strategies.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 511296-88-1\u003c\/li\u003e\n\u003cli\u003eCategory: Life Science \u0026gt; Cell Biology \u0026gt; Cancer Research\u003c\/li\u003e\n\u003cli\u003ePack sizes: Not specified\u003c\/li\u003e\n\u003cli\u003ePhysical form: Not specified\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from light\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis compound should be stored in a cool, dry place, away from direct light to maintain its chemical stability. It is recommended to use airtight containers to prevent moisture absorption and contamination. Due to its chemical nature, it should be handled with appropriate personal protective equipment, such as gloves and safety goggles, to ensure laboratory safety. Avoid exposure to incompatible substances to prevent any adverse reactions. Proper labeling of containers is essential for safe handling and storage. Regular monitoring of storage conditions ensures the compound remains effective for research applications.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"100mg","offer_id":48086198616282,"sku":"TCI2510C282617701","price":29398000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C2826.jpg?v=1769144350"},{"product_id":"tci2510c285417731","title":"TCI C2854 77-53-2 Cedrol","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eCedrol (77-53-2) is an organic compound classified as a phenolic compound, widely utilized in life science research. It plays a crucial role in biochemical and pharmaceutical studies, serving as a key reagent in experimental setups. Its unique chemical structure and biological activity make it an essential component for researchers working on drug development, organic synthesis, and bioactive compound analysis. Cedrol is particularly valued for its versatility in supporting a wide range of scientific inquiries, from basic research to advanced experimental applications.\u003c\/p\u003e\n\u003cp\u003eCedrol is preferred due to its moderate polarity and solubility in organic solvents such as ethyl acetate and ethanol. These properties enable it to be effectively used in various chemical reactions and synthesis processes. Its high biological activity, including antioxidant and antimicrobial properties, further enhances its applicability in health-related research. The compound’s stability under specific conditions also contributes to its reliability in laboratory settings, ensuring consistent results over time.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, Cedrol is commonly used in pharmaceutical, biotechnology, and chemical research. It is a staple in academic and industrial research institutions, supporting the development of new drugs and bioactive compounds. Its availability and well-documented properties make it a trusted choice for researchers aiming to advance scientific knowledge and innovation.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003ePharmaceutical research utilizes Cedrol for the development of new drugs due to its bioactive properties and chemical versatility.\u003c\/li\u003e\n\u003cli\u003eOrganic synthesis experiments benefit from Cedrol’s solubility in organic solvents and its role in complex molecule creation.\u003c\/li\u003e\n\u003cli\u003eAntimicrobial studies often incorporate Cedrol because of its known antimicrobial activity, aiding in the evaluation of natural compounds.\u003c\/li\u003e\n\u003cli\u003eBiochemical assays use Cedrol as a reagent to test the effects of phenolic compounds on cellular processes and enzyme activity.\u003c\/li\u003e\n\u003cli\u003eHealth-related research employs Cedrol to explore its antioxidant properties and potential applications in therapeutic formulations.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 77-53-2\u003c\/li\u003e\n\u003cli\u003eCategory: Life Science \u0026gt; Biochemicals and Reagents \u0026gt; Crude Medicine Ingredients for Research and Experimental Use\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per standard laboratory supply\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid or liquid, depending on the specific product variant\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from direct sunlight and moisture\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eCedrol should be stored in a cool, dry environment to maintain its chemical stability and prevent degradation. It is recommended to keep it in airtight containers to minimize exposure to moisture and air, which can affect its quality over time. When handling Cedrol, researchers should use appropriate personal protective equipment, such as gloves and safety goggles, to ensure safety. It is important to avoid contact with skin and eyes, and to work in a well-ventilated area to reduce inhalation risks. Proper labeling of storage containers is essential for safe handling and to prevent accidental misuse. Regular monitoring of storage conditions ensures the compound remains suitable for use in laboratory applications.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48086199795930,"sku":"TCI2510C285417731","price":1771000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48086199828698,"sku":"TCI2510C285417732","price":6156000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C2854.jpg?v=1767098891"},{"product_id":"tci2510c294217843","title":"TCI C2942 427-51-0 Cyproterone Acetate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C2942 is Cyproterone Acetate, a synthetic steroid compound supplied as a pharmaceutical research reagent for experimental laboratory use. The molecule belongs to the modified pregnane steroid family and is widely documented in the endocrinology literature as both an antiandrogenic compound and a progestin. In a research setting, this material serves as a test compound for hormone receptor investigations, as an analytical reference substance during the development of steroid assay methods, and as a subject of medicinal chemistry studies examining the relationship between steroid structure and biological activity.\u003c\/p\u003e\n\u003cp\u003eThe properties that make this material valuable to researchers centre on its rigid, stereochemically defined four-ring steroid framework, complemented by an acetate ester group and a characteristic substitution pattern that distinguishes it from naturally occurring steroid hormones. Because the ring skeleton is conformationally rigid, the spatial orientation of its functional groups remains highly consistent from experiment to experiment, which makes the compound well suited to receptor binding studies and molecular modelling work. As a steroid, it is generally a crystalline solid with limited solubility in water but dissolves in organic solvents such as ethanol or dimethyl sulfoxide.\u003c\/p\u003e\n\u003cp\u003eWithin Indonesian laboratories, this reagent is typically handled in university pharmacy and pharmaceutical chemistry departments, biomedical and endocrinology research groups, and analytical method development units that work with steroid compounds. It is used strictly for experimental purposes, prepared as stock solutions in a suitable organic solvent before dilution into working systems, and applied in receptor studies, comparative analytical runs, and structure–activity investigations conducted under standard laboratory protocols.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eHormone receptor binding studies — the rigid steroid skeleton gives a consistent spatial arrangement of functional groups, making interaction data with receptor preparations reproducible between experimental runs.\u003c\/li\u003e\n\u003cli\u003eAnalytical reference material for steroid assay development — serves as a comparison substance when chromatographic or spectroscopic methods for steroid compounds are being established and validated in the laboratory.\u003c\/li\u003e\n\u003cli\u003eMedicinal chemistry structure–activity research — its distinctive substitution pattern relative to natural steroid hormones makes it a useful reference point for studying how structural modification affects biological activity.\u003c\/li\u003e\n\u003cli\u003eMolecular modelling and computational chemistry work — the stereochemically defined, conformationally rigid four-ring framework provides reliable geometry input for docking simulations and comparative structural analysis studies.\u003c\/li\u003e\n\u003cli\u003eEndocrinology teaching and experimental investigation — widely documented in the endocrinology literature as an antiandrogen and progestin, giving researchers ample published context to design and interpret experimental work.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 427-51-0\u003c\/li\u003e\n\u003cli\u003eCategory: Life Science \u0026gt; Biochemicals and Reagents \u0026gt; Pharmaceutical Research Reagents (for Experimental Use)\u003c\/li\u003e\n\u003cli\u003eProduct code: C2942\u003c\/li\u003e\n\u003cli\u003ePhysical form: crystalline solid; limited solubility in water, soluble in organic solvents such as ethanol or dimethyl sulfoxide\u003c\/li\u003e\n\u003cli\u003ePack sizes: available in standard research quantities — please refer to the catalogue listing for the packaging options offered\u003c\/li\u003e\n\u003cli\u003eStorage: keep in a tightly closed container in a cool, dry place away from light\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eStore the material in its original tightly closed container, in a cool, dry location protected from direct light and moisture, and follow the storage instructions printed on the product label and safety data sheet. Amber glass vials or the supplier's original packaging are appropriate containers; avoid transferring the solid into containers that do not seal properly. Handle the compound in a well-ventilated area or fume hood using gloves, safety glasses, and a laboratory coat, and avoid generating dust when weighing the crystalline solid. Stock solutions prepared in ethanol or dimethyl sulfoxide should be clearly labelled with the solvent, concentration, and preparation date, kept tightly capped, and handled only by trained personnel. This product is intended for experimental laboratory use only and is not for human or veterinary application; dispose of residues and contaminated consumables through the laboratory's established chemical waste procedures.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"200mg","offer_id":48086204023002,"sku":"TCI2510C294217843","price":2671000.0,"currency_code":"IDR","in_stock":true},{"title":"1g","offer_id":48086204055770,"sku":"TCI2510C294217844","price":9305000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C2942.jpg?v=1768204716"},{"product_id":"tci2510c300917931","title":"TCI C3009 168555-66-6 Combretastatin A4 Phosphate Disodium Salt","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C3009 Combretastatin A4 Phosphate Disodium Salt is a research reagent supplied as the disodium phosphate salt of combretastatin A4, a stilbenoid compound widely studied as a tumor vascular disrupting agent and an inhibitor of tubulin polymerization. In the laboratory, this material serves as a model molecule for examining microtubule dynamics, antiangiogenesis mechanisms, and the behavior of prodrug compounds that are activated enzymatically. Because it is classified as a research reagent, the product is intended exclusively for scientific experimentation in controlled environments, and is not for diagnostic or therapeutic use in humans or animals.\u003c\/p\u003e\n\u003cp\u003eThe characteristic that makes this compound a frequent choice is its disodium phosphate salt form. Modification with the phosphate group improves solubility in aqueous media compared with the free phenolic form, so researchers can more easily prepare stock solutions for cell culture assays without depending entirely on organic solvents such as DMSO. This prodrug property is also conceptually attractive: removal of the phosphate group by phosphatases yields the active form, which is why the compound is often used as a concrete teaching and demonstration example of enzymatically activated prodrug design. The combination of improved aqueous handling and a well-documented mechanism of action makes the material practical for routine bench work as well as for method development.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this reagent is typically used in university research groups, pharmaceutical development units, and drug discovery laboratories working on drug delivery systems (DDS). It commonly supports cell culture based screening, mechanistic studies of microtubule-targeting compounds, and comparative work on prodrug activation. Work is normally carried out in laboratories equipped with fume hoods, biosafety cabinets, and cold storage, with material handled according to institutional research procedures and the supplier's safety data sheet.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eTubulin polymerization studies: the compound is a well-characterized inhibitor of tubulin polymerization, making it a dependable reference material when researchers need a known-active molecule for in vitro assays.\u003c\/li\u003e\n\u003cli\u003eMicrotubule dynamics research: because its mechanism targets the microtubule system, the reagent is suitable as a model molecule for observing how cytoskeletal assembly and disassembly respond to chemical perturbation.\u003c\/li\u003e\n\u003cli\u003eAntiangiogenesis and vascular disruption studies: as a compound widely studied for tumor vascular disrupting activity, it supports mechanistic investigation of how vascular structures respond in controlled experimental systems.\u003c\/li\u003e\n\u003cli\u003eProdrug activation research: the phosphate group is removed by phosphatases to release the active form, so the material serves as a practical experimental example of enzymatically activated prodrug behavior.\u003c\/li\u003e\n\u003cli\u003eDrug delivery systems (DDS) development: improved aqueous solubility relative to the free phenolic form makes the salt convenient for formulation and delivery experiments that require preparation of aqueous stock solutions.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS Number: 168555-66-6\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Pharmaceutical Development and Drug Discovery Research Reagents \u0026gt; Drug Delivery Systems (DDS)\u003c\/li\u003e\n\u003cli\u003eProduct code: C3009\u003c\/li\u003e\n\u003cli\u003ePack sizes: available in the pack sizes listed by the manufacturer for this catalog item\u003c\/li\u003e\n\u003cli\u003eStorage: store according to the conditions stated on the manufacturer's label and safety data sheet\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eStore the reagent in its original tightly closed container, protected from moisture and direct light, and follow the storage temperature stated on the manufacturer's label and safety data sheet. Amber glass vials or the supplied primary container are appropriate; transfer only what is needed and reseal promptly to limit exposure to humid air. Prepared aqueous stock solutions should be labeled with contents and preparation date and kept in clearly identified containers. Handle the material as a research chemical of unknown toxicological profile: work in a fume hood or biosafety cabinet where appropriate, wear a laboratory coat, nitrile gloves, and eye protection, avoid inhalation of dust and skin contact, and dispose of residues and contaminated consumables through the institution's chemical waste procedures. Keep the safety data sheet accessible to all users.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"20mg","offer_id":48086207398106,"sku":"TCI2510C300917931","price":4667000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C3009.jpg?v=1768204722"},{"product_id":"tci2510c336318400","title":"TCI C3363 35825-57-1 Cryptotanshinone","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eCryptotanshinone is a naturally occurring compound derived from the *Salvia miltiorrhiza* plant, commonly known as *Danshen* in traditional Chinese medicine. This compound plays a significant role in life science laboratories, where it is utilized for studying its biological activities, including antioxidant, anti-inflammatory, and potential therapeutic effects on chronic diseases. Its presence in research settings allows scientists to explore its pharmacological properties and mechanisms of action. Due to its stability and availability, Cryptotanshinone is a valuable resource for experimental studies in both academic and industrial research environments.\u003c\/p\u003e\n\u003cp\u003eThe compound's unique molecular structure enables it to interact with various biological targets such as enzymes and cell receptors, making it a versatile tool in biochemical research. Its chemical properties also allow for testing its stability under different experimental conditions, which is crucial for reproducibility and accuracy in scientific studies. Additionally, its high purity and consistent quality ensure reliable results, making it a preferred choice for researchers seeking precision in their experiments.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, Cryptotanshinone is widely used in health and pharmacology-related research. Local research institutions frequently incorporate this compound into their studies to investigate its potential applications in drug development and disease treatment. Its relevance in both traditional and modern scientific contexts underscores its importance in the Indonesian scientific community.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003ePharmacological research for studying the compound's therapeutic potential in chronic disease treatment\u003c\/li\u003e\n\u003cli\u003eBiochemical experiments to analyze its antioxidant and anti-inflammatory properties\u003c\/li\u003e\n\u003cli\u003eDrug development studies to evaluate its interaction with biological targets such as enzymes and receptors\u003c\/li\u003e\n\u003cli\u003eStability testing under various experimental conditions to ensure reproducibility of results\u003c\/li\u003e\n\u003cli\u003eResearch on traditional Chinese medicine to explore its modern scientific applications\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 35825-57-1\u003c\/li\u003e\n\u003cli\u003eCategory: Life Science \u0026gt; Biochemicals and Reagents \u0026gt; Crude Medicine Ingredients for Research and Experimental Use\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in standard research quantities\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid powder\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from light\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eCryptotanshinone should be stored in a cool, dry environment to maintain its stability and prevent degradation. It is recommended to use airtight containers to protect it from moisture and contaminants. Due to its chemical nature, it should be handled with appropriate personal protective equipment, such as gloves and safety goggles, to ensure laboratory safety. The compound is generally non-hazardous but should be stored away from incompatible substances. Regular monitoring of storage conditions is essential to maintain its quality and effectiveness for research purposes. Proper labeling and documentation of storage locations are also important for safe laboratory management.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25mg","offer_id":48086237708506,"sku":"TCI2510C336318400","price":2306000.0,"currency_code":"IDR","in_stock":true},{"title":"100mg","offer_id":48086237741274,"sku":"TCI2510C336318401","price":6493000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C3363.jpg?v=1767099508"},{"product_id":"tci2510c339018435","title":"TCI C3390 183133-96-2 Cabazitaxel","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eCabazitaxel is a chemical compound classified as an antitumor agent, widely used in biomedical and pharmacological research for the development of cancer therapies. As a key component in the study of cellular mechanisms, it plays a vital role in laboratories focused on oncology and drug discovery. Its molecular structure allows it to interact with microtubule proteins, thereby inhibiting the proliferation of cancer cells. This makes it an essential tool for understanding the biological processes underlying tumor growth and resistance.\u003c\/p\u003e\n\u003cp\u003eThe compound is preferred due to its chemical stability under controlled conditions and its ability to dissolve in various solvents, offering flexibility in experimental setups. Its sensitivity to light and high temperatures necessitates careful handling, but this also ensures that it remains effective when stored properly. The specificity of its interactions with cellular targets makes it ideal for applications requiring precise measurement and controlled chemical reactions.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, Cabazitaxel is commonly used in cancer therapy research, drug development, and toxicity testing. Its availability supports academic and industrial research efforts, enabling scientists to explore new therapeutic approaches and evaluate the efficacy of antitumor compounds. Its role in advancing pharmaceutical innovation is critical, especially in regions where access to advanced research tools is essential.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eCancer Therapy Research: Cabazitaxel is used to study the mechanisms of tumor cell proliferation and the effectiveness of antitumor agents in laboratory settings.\u003c\/li\u003e\n\u003cli\u003eDrug Development: It serves as a key reagent in the synthesis of active compounds and the evaluation of new pharmaceutical formulations.\u003c\/li\u003e\n\u003cli\u003eToxicity Testing: Cabazitaxel is employed to assess the safety and potential side effects of antitumor drugs in controlled experimental conditions.\u003c\/li\u003e\n\u003cli\u003eBiochemical Analysis: Its solubility in various solvents makes it suitable for use in assays that require precise chemical interactions and reaction control.\u003c\/li\u003e\n\u003cli\u003ePharmacological Studies: It is used to investigate the biological activity of antitumor compounds and their impact on cellular processes.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 183133-96-2\u003c\/li\u003e\n\u003cli\u003eCategory: Life Science \u0026gt; Biochemicals and Reagents \u0026gt; Antibiotics\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in standard laboratory quantities\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dark place away from light and heat\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eCabazitaxel should be stored in a cool, dark environment to prevent degradation due to light and high temperatures. It is recommended to use amber-colored glass containers to minimize exposure to light. The compound should be kept in a dry place with controlled humidity to maintain its chemical stability. When handling, it is important to use appropriate personal protective equipment, such as gloves and safety goggles, to ensure safety. Due to its sensitivity, it should be handled in a fume hood to prevent inhalation of vapors. Proper labeling and storage conditions are essential to maintain its effectiveness and ensure safe laboratory practices.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25mg","offer_id":48086242066650,"sku":"TCI2510C339018435","price":2924000.0,"currency_code":"IDR","in_stock":true},{"title":"100mg","offer_id":48086242099418,"sku":"TCI2510C339018436","price":8657000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C3390.jpg?v=1767099541"},{"product_id":"tci2510c344918491","title":"TCI C3449 285986-88-1 CCG-1423","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eCCG-1423 is a chemical compound widely used in cancer research to investigate the mechanisms of cancer cell growth and the development of new therapies. As a key component in life science research, it plays a crucial role in cell biology laboratories by enabling scientists to study biochemical pathways involved in cancer progression. This compound is essential for advancing understanding of oncogenic processes and identifying potential therapeutic targets. Its application supports both fundamental and applied research in the field of oncology.\u003c\/p\u003e\n\u003cp\u003eThe compound’s chemical stability and molecular complexity make it a preferred choice for laboratory use. Its ability to interact specifically with proteins and enzymes involved in cancer-related pathways enhances the accuracy of experimental results. This stability ensures consistent performance across various experimental conditions, making it reliable for both small-scale and large-scale studies. Additionally, its compatibility with standard laboratory protocols allows for seamless integration into existing research workflows.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, CCG-1423 is commonly used in cancer research conducted by academic institutions and research organizations. It supports local scientists in meeting international research standards and contributes to the development of new cancer treatments. Its use is integral to expanding knowledge about cancer biology and improving therapeutic strategies in the region.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eCancer Cell Growth Analysis: CCG-1423 is ideal for studying how cancer cells proliferate and respond to various stimuli, providing insights into tumor development.\u003c\/li\u003e\n\u003cli\u003eBiochemical Pathway Investigation: The compound enables researchers to explore the molecular mechanisms underlying cancer progression, aiding in the discovery of new therapeutic targets.\u003c\/li\u003e\n\u003cli\u003eDrug Development Testing: It is used in screening potential anti-cancer agents, helping to identify compounds that can inhibit cancer-related pathways effectively.\u003c\/li\u003e\n\u003cli\u003eMolecular Interaction Studies: CCG-1423 facilitates the examination of interactions between proteins and enzymes involved in cancer, supporting detailed biochemical analyses.\u003c\/li\u003e\n\u003cli\u003eExperimental Model Validation: It supports the validation of cancer research models, ensuring the accuracy and reproducibility of experimental outcomes.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 285986-88-1\u003c\/li\u003e\n\u003cli\u003eCategory: Life Science \u0026gt; Cell Biology \u0026gt; Cancer Research\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in standard laboratory quantities\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid or liquid, depending on formulation\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from direct light\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eCCG-1423 should be stored in a cool, dry environment, away from direct sunlight and sources of heat. It is recommended to use airtight containers to prevent moisture absorption and contamination. The compound should be handled with appropriate personal protective equipment, such as gloves and safety goggles, to ensure laboratory safety. Due to its chemical stability, it does not require refrigeration but should be kept in a secure location to avoid accidental exposure. Proper labeling of containers is essential to maintain safety and prevent misuse in the laboratory setting.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25mg","offer_id":48086248423642,"sku":"TCI2510C344918491","price":4638000.0,"currency_code":"IDR","in_stock":true},{"title":"100mg","offer_id":48086248456410,"sku":"TCI2510C344918492","price":13885000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C3449.jpg?v=1768817094"},{"product_id":"tci2510c349418553","title":"TCI C3494 2415-24-9 Catalpol","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eCatalpol is a chemical compound classified under glycosides, widely utilized in chemical and biological research. It plays a significant role in laboratory settings where the study of bioactive compounds, pharmacological effects, and antioxidant activities is required. As a key component in various scientific investigations, Catalpol is essential for experiments involving molecular structure analysis, biological activity testing, and molecular interaction studies in biological environments. Its presence in research areas such as pharmacology and phytochemistry highlights its importance in understanding natural compounds and their potential therapeutic applications.\u003c\/p\u003e\n\u003cp\u003eCatalpol is valued for its chemical stability and solubility in specific organic solvents like ethyl acetate and acetone. These properties make it highly compatible with analytical techniques such as chromatography and spectroscopy, enabling accurate and reliable experimental results. Additionally, its antitumor and anti-inflammatory properties have made it a sought-after material in both pharmacological and biochemical studies. The compound’s versatility and effectiveness in various experimental setups contribute to its popularity among researchers.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, Catalpol is commonly used in pharmaceutical, molecular biology, and organic chemistry research. It is a preferred choice for experiments requiring high biological activity, especially in studies involving natural compounds. Its consistent performance and reliability make it a trusted material for researchers aiming to explore the potential of bioactive substances in both academic and applied settings.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eUsed in pharmacological research for studying the antitumor and anti-inflammatory effects of natural compounds.\u003c\/li\u003e\n\u003cli\u003eApplied in biochemical studies to analyze the antioxidant properties of bioactive substances.\u003c\/li\u003e\n\u003cli\u003eEmployed in molecular biology experiments for investigating molecular interactions and structural analysis.\u003c\/li\u003e\n\u003cli\u003eUtilized in organic chemistry for the synthesis and characterization of glycoside derivatives.\u003c\/li\u003e\n\u003cli\u003eIntegrated into analytical techniques such as HPLC and UV-Vis spectroscopy for compound identification and quantification.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 2415-24-9\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Chemical Biology \u0026gt; Glycoscience\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per standard laboratory requirements\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid powder\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from light and moisture\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eCatalpol should be stored in a cool, dry environment, away from direct light and moisture to maintain its chemical stability. It is recommended to use airtight containers made of glass or high-density polyethylene to prevent contamination and degradation. Due to its solubility in organic solvents, it should be handled in a well-ventilated area to avoid inhalation of vapors. Laboratory personnel should wear appropriate personal protective equipment, including gloves and safety goggles, when handling the compound. Catalpol is non-hazardous under normal conditions but should be kept out of reach of children and not exposed to incompatible materials. Proper labeling and storage practices ensure the safety and effectiveness of the compound in research applications.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"250mg","offer_id":48086255141082,"sku":"TCI2510C349418553","price":7027000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C3494.jpg?v=1767099684"},{"product_id":"tci2510c357518663","title":"TCI C3575 194423-06-8 CL-387785","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C3575, with the CAS number 194423-06-8, is a chemical compound widely used in life science research applications. It belongs to the category of enzymes, enzyme inhibitors, and enzyme substrates, playing a crucial role in biochemical reactions by facilitating catalytic processes. This compound is essential for experiments that require enzymatic activity, such as enzyme activity assays, substrate testing, and metabolic pathway studies. Its presence in laboratory settings ensures that researchers can achieve precise and reproducible results in their investigations.\u003c\/p\u003e\n\u003cp\u003eThe compound’s high purity and consistent quality across batches make it a preferred choice for scientific research. Its chemical stability allows it to perform reliably under various experimental conditions, including different temperatures and pH levels. These properties ensure that it remains effective in a wide range of applications, making it a trusted material for both academic and industrial research. The reliability of TCI C3575 also supports the accuracy of data obtained in biochemical experiments.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, TCI C3575 is commonly used in biotechnology, pharmaceutical, and medical research. It is particularly valuable for studies involving enzyme kinetics, metabolic profiling, and drug development. Its availability and performance make it an essential tool for researchers aiming to maintain high standards in their experimental work. The compound’s versatility and reliability contribute significantly to the advancement of scientific research in Indonesia.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eEnzyme Activity Assays – This compound is ideal for measuring enzyme activity due to its role as a substrate or inhibitor, allowing researchers to assess catalytic efficiency in controlled environments.\u003c\/li\u003e\n\u003cli\u003eSubstrate Testing – It is frequently used to evaluate how enzymes interact with substrates, providing insights into reaction mechanisms and enzyme specificity.\u003c\/li\u003e\n\u003cli\u003eMetabolic Pathway Analysis – Its involvement in biochemical reactions makes it suitable for studying metabolic pathways and enzyme-driven processes in biological systems.\u003c\/li\u003e\n\u003cli\u003eDrug Development Research – It supports the screening of potential drug candidates by analyzing enzyme interactions and metabolic effects in vitro.\u003c\/li\u003e\n\u003cli\u003eBiotechnology Applications – Its use in enzyme-based processes aids in the development of biotechnological products, including industrial enzymes and bioactive compounds.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 194423-06-8\u003c\/li\u003e\n\u003cli\u003eCategory: Life Science \u0026gt; Biochemicals and Reagents \u0026gt; Enzymes, Enzyme Inhibitors, Enzyme Substrates\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per standard laboratory requirements\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid or liquid, depending on the specific product variant\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from direct sunlight and moisture\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis compound should be stored in a cool, dry environment to maintain its chemical stability and prevent degradation. It is recommended to use airtight containers to protect it from moisture and contaminants. When handling, ensure that appropriate personal protective equipment is worn, such as gloves and safety goggles, to minimize exposure. The compound should be kept away from incompatible substances to avoid any adverse reactions. Proper labeling of storage containers is essential for safe handling and easy identification. Regular inspection of storage conditions ensures the material remains in optimal condition for use in laboratory experiments.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25mg","offer_id":48086265004250,"sku":"TCI2510C357518663","price":7422000.0,"currency_code":"IDR","in_stock":true},{"title":"100mg","offer_id":48086265037018,"sku":"TCI2510C357518664","price":21276000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C3575.jpg?v=1768817122"},{"product_id":"tci2510c358418676","title":"TCI C3584 3895-92-9 Chelerythrine Chloride","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eChelerythrine Chloride is a chemical compound widely utilized in scientific research, particularly in the fields of biochemistry and pharmacology. This compound is derived from the plant *Chelidonium majus* and is recognized for its significant pharmacological activity. In laboratory settings, it serves as a key reagent for various experiments, including the study of biological mechanisms, drug development, and the investigation of natural compounds. Its role is essential in advancing research that explores the potential therapeutic applications of plant-derived substances.\u003c\/p\u003e\n\u003cp\u003eChelerythrine Chloride is valued for its complex chemical structure and polar nature, which allows it to dissolve in organic solvents such as ethyl acetate and methanol. These properties make it highly versatile for use in chemical reactions and extraction processes. Additionally, its stability under certain conditions ensures that it remains effective for extended periods, facilitating long-term research projects. This combination of solubility and stability makes it a preferred choice for researchers working with natural compounds.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, Chelerythrine Chloride is commonly used in research focused on the biological effects of natural substances. It plays a vital role in the development of pharmaceutical products and biomedical research aimed at treating chronic diseases. Its presence in research studies helps scientists better understand the pharmacological properties of plant-derived compounds, contributing to the advancement of medical science in the region.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eDrug development research utilizes Chelerythrine Chloride to study the pharmacological properties of natural compounds and their potential therapeutic applications.\u003c\/li\u003e\n\u003cli\u003eAnti-inflammatory and antioxidant activity testing benefits from its ability to interact with biological systems, making it ideal for evaluating natural compound efficacy.\u003c\/li\u003e\n\u003cli\u003eBiochemical experiments leverage its solubility in organic solvents to facilitate extraction and reaction processes in laboratory settings.\u003c\/li\u003e\n\u003cli\u003eNatural product isolation and purification studies rely on its chemical structure and stability to ensure consistent results in research.\u003c\/li\u003e\n\u003cli\u003eChronic disease research incorporates Chelerythrine Chloride to explore its potential role in developing treatments for long-term health conditions.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 3895-92-9\u003c\/li\u003e\n\u003cli\u003eCategory: Life Science \u0026gt; Biochemicals and Reagents \u0026gt; Crude Medicine Ingredients for Research and Experimental Use\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in standard research quantities as per supplier specifications\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid powder\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from light and moisture\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eChelerythrine Chloride should be stored in a cool, dry environment, away from direct sunlight and moisture to maintain its chemical integrity. It is recommended to use airtight containers made of glass or high-density polyethylene to prevent contamination and degradation. Due to its polar nature, it is important to handle the compound with care during preparation and use to avoid any unintended chemical interactions. In laboratory settings, proper personal protective equipment such as gloves and safety goggles should be worn when handling this compound to ensure safety. Regular monitoring of storage conditions is also advised to ensure the compound remains stable and effective for research purposes.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25mg","offer_id":48086267527386,"sku":"TCI2510C358418676","price":8124000.0,"currency_code":"IDR","in_stock":true},{"title":"100mg","offer_id":48086267560154,"sku":"TCI2510C358418677","price":22457000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C3584.jpg?v=1767099809"},{"product_id":"tci2510c360118697","title":"TCI C3601 163042-96-4 Chloro-IB-MECA","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eChloro-IB-MECA (1-(2-Chloro-4-iodophenyl)-3-(1,3-dihydro-1,3-dioxo-2H-isoindol-2-yl)urea) is a chemical compound widely used in life science research. It serves as a key reagent in biochemical and pharmaceutical studies, playing a crucial role in the synthesis of bioactive compounds. This compound is commonly found in laboratories where researchers are working on the development of new drugs and the study of biological activities. Its presence in such environments highlights its importance in advancing scientific understanding and innovation.\u003c\/p\u003e\n\u003cp\u003eThe compound's complex chemical structure contributes to its high reactivity, making it a preferred choice for various laboratory applications. Its ability to participate in chemical reactions under different conditions allows for precise control over synthetic processes. Additionally, its stability under certain conditions ensures consistent results, which is essential in scientific research. These properties make Chloro-IB-MECA a reliable and versatile material for researchers aiming for accuracy and reproducibility in their experiments.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, Chloro-IB-MECA is frequently used in pharmacological and biochemical research. It is particularly valuable in the study of synthetic compounds and their biological activities. Researchers in Indonesia rely on this compound for its reliability and effectiveness in experimental settings, contributing to advancements in drug development and biological studies.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003ePharmacological research utilizes Chloro-IB-MECA to investigate the biological activity of synthetic compounds, supporting the development of new therapeutic agents.\u003c\/li\u003e\n\u003cli\u003eBiochemical studies employ this compound as a reagent in the synthesis of bioactive molecules, enabling the exploration of molecular mechanisms.\u003c\/li\u003e\n\u003cli\u003eDrug discovery projects benefit from Chloro-IB-MECA's reactivity, allowing for the creation of compounds with targeted biological effects.\u003c\/li\u003e\n\u003cli\u003eAnalytical chemistry applications use the compound to test the efficacy and stability of synthesized materials under various experimental conditions.\u003c\/li\u003e\n\u003cli\u003eMolecular biology experiments incorporate Chloro-IB-MECA to study interactions between chemical structures and biological systems, enhancing understanding of molecular behavior.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 163042-96-4\u003c\/li\u003e\n\u003cli\u003eCategory: Life Science \u0026gt; Biochemicals and Reagents \u0026gt; Nucleosides, Nucleotides, Oligonucleotides\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in standard laboratory quantities as per supplier specifications\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid, as per standard chemical product description\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from direct sunlight and moisture\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eChloro-IB-MECA should be stored in a cool, dry environment to maintain its chemical stability and prevent degradation. It is recommended to keep the compound in a sealed container to minimize exposure to air and moisture. Proper labeling of storage containers is essential to ensure safe handling and prevent accidental contamination. Laboratory personnel should wear appropriate personal protective equipment, such as gloves and safety goggles, when handling this compound. Regular inspection of storage conditions is advised to ensure compliance with safety standards. The compound should not be stored near incompatible materials to avoid potential chemical reactions. Maintaining a controlled environment is crucial for preserving the integrity of the material during long-term storage.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"10mg","offer_id":48086269264090,"sku":"TCI2510C360118697","price":3233000.0,"currency_code":"IDR","in_stock":true},{"title":"50mg","offer_id":48086269296858,"sku":"TCI2510C360118698","price":11216000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C3601.jpg?v=1769180457"},{"product_id":"tci2510c381818913","title":"TCI C3818 267243-28-7 Canertinib","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eCanertinib is a chemical compound widely used in biochemical and pharmacological research. It belongs to the category of enzyme inhibitors, playing a crucial role in studying enzyme mechanisms and their activity suppression. As a potent inhibitor of the Epidermal Growth Factor Receptor (EGFR), Canertinib is frequently employed in cancer-related research and therapeutic response studies. Its application in laboratories allows scientists to explore cellular proliferation processes and drug development pathways. This compound is essential for understanding the molecular interactions that influence disease progression and treatment efficacy.\u003c\/p\u003e\n\u003cp\u003eCanertinib is valued for its chemical stability and specificity in targeting proteins. Its complex molecular structure enables precise interactions with specific protein targets, making it ideal for high-precision research. The compound exhibits strong inhibitory activity against enzymes, which is vital for experiments requiring accuracy and reproducibility. Its reliability and consistent performance make it a preferred choice for various biochemical and pharmaceutical applications. The quality of Canertinib ensures that it meets the rigorous standards required in modern scientific research.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, Canertinib is commonly used in biomedical and pharmaceutical research. It supports studies on cancer biology, drug development, and molecular interactions. Many research institutions and universities in Indonesia rely on Canertinib for its effectiveness and versatility in experimental settings. Its presence in local laboratories underscores its importance in advancing scientific knowledge and innovation in the region.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eEnzyme Inhibition Studies – Canertinib is ideal for investigating enzyme activity suppression and mechanism of action due to its strong inhibitory properties.\u003c\/li\u003e\n\u003cli\u003eCancer Research – Its EGFR inhibition makes it a key tool in studying tumor growth and therapeutic responses in oncology experiments.\u003c\/li\u003e\n\u003cli\u003eDrug Development – Canertinib is used in pharmaceutical research to evaluate potential therapeutic agents and their molecular interactions.\u003c\/li\u003e\n\u003cli\u003eMolecular Interaction Studies – The compound’s specificity allows researchers to explore protein-ligand interactions and signaling pathways.\u003c\/li\u003e\n\u003cli\u003eBiochemical Assays – Its stability and reactivity make it suitable for various biochemical tests and enzyme activity measurements.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 267243-28-7\u003c\/li\u003e\n\u003cli\u003eCategory: Life Science \u0026gt; Biochemicals and Reagents \u0026gt; Enzymes, Enzyme Inhibitors, Enzyme Substrates\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in standard laboratory quantities\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid powder\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from light\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eCanertinib should be stored in a cool, dry environment, away from direct sunlight and moisture. It is recommended to use airtight containers to prevent contamination and maintain its chemical stability. Due to its potential reactivity, it should be handled with appropriate personal protective equipment, such as gloves and safety goggles. Proper ventilation is essential when working with the compound to minimize exposure. Storage conditions should be consistent to ensure the integrity of the material. All handling procedures should follow standard laboratory safety protocols to ensure the safety of personnel and the accuracy of experimental results.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25mg","offer_id":48086292725978,"sku":"TCI2510C381818913","price":4610000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C3818.jpg?v=1769180462"},{"product_id":"tci2510c389219010","title":"TCI C3892 149394-66-1 Cidofovir Dihydrate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eCidofovir Dihydrate is a chemical compound widely used in life science research, particularly in the study of antibiotics and drug development. This reagent plays a crucial role in laboratories where antiviral activity is being investigated. Its ability to inhibit the replication of certain viruses makes it an essential tool for researchers working on viral infections. As a biochemical reagent, it is commonly used in various experimental setups that require a stable and effective antiviral agent.\u003c\/p\u003e\n\u003cp\u003eOne of the key properties that make Cidofovir Dihydrate a preferred choice is its chemical stability under specific conditions. This stability ensures that the compound maintains its potency over time, making it suitable for long-term research applications. Additionally, its dihydrate form facilitates easier dissolution and handling, which is beneficial for a wide range of laboratory experiments. The compound's resistance to degradation further enhances its reliability in research settings.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, Cidofovir Dihydrate is frequently used in pharmacological, virological, and microbiological studies. Researchers rely on this compound due to its availability and consistent chemical properties. It is a go-to reagent for experiments that require a stable and effective antiviral agent, supporting advancements in both academic and applied research. Its presence in Indonesian research institutions underscores its importance in the scientific community.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eToxicity testing involves using Cidofovir Dihydrate to assess the safety and potential side effects of antiviral compounds in biological systems.\u003c\/li\u003e\n\u003cli\u003eDrug development research utilizes this reagent to evaluate the efficacy of new antiviral agents against specific viral strains.\u003c\/li\u003e\n\u003cli\u003eVirological studies benefit from Cidofovir Dihydrate’s antiviral activity, enabling researchers to investigate viral replication and inhibition mechanisms.\u003c\/li\u003e\n\u003cli\u003ePharmacological experiments often incorporate this compound to study its interaction with cellular processes and therapeutic applications.\u003c\/li\u003e\n\u003cli\u003eMicrobiological research uses Cidofovir Dihydrate to explore its impact on viral infections and its role in developing targeted treatments.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 149394-66-1\u003c\/li\u003e\n\u003cli\u003eCategory: Life Science \u0026gt; Biochemicals and Reagents \u0026gt; Antibiotics\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per supplier specifications\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from moisture and direct sunlight\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eCidofovir Dihydrate should be stored in a cool, dry environment to maintain its chemical stability and prevent degradation. It is recommended to keep the compound in a sealed container to avoid exposure to moisture and air, which could affect its potency. Laboratory personnel should handle the reagent with care, using appropriate personal protective equipment such as gloves and safety goggles. Since it is a solid form, it is generally easy to manage but should be stored in a location that is inaccessible to children and unauthorized individuals. Regular monitoring of storage conditions ensures the integrity of the compound remains intact for research use. Proper labeling of containers is essential to prevent confusion and ensure safe handling in laboratory settings.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"50mg","offer_id":48086300688602,"sku":"TCI2510C389219010","price":3345000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C3892.jpg?v=1767100257"},{"product_id":"tci2510c391819035","title":"TCI C3918 288383-20-0 Cediranib","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C3918 288383-20-0 Cediranib is a chemical compound widely used in cancer research to inhibit the growth of cancer cells. As a tyrosine kinase inhibitor, Cediranib targets specific proteins involved in the proliferation and metastasis of cancer cells. This compound plays a critical role in laboratory settings where researchers are investigating the molecular mechanisms underlying cancer progression. Its application extends to various experimental models, making it an essential tool for scientists working in cell biology and oncology.\u003c\/p\u003e\n\u003cp\u003eCediranib is preferred due to its chemical stability and solubility in organic solvents, which allows it to be easily incorporated into a wide range of experimental protocols. Its high biological activity ensures reliable results in assays designed to evaluate its effects on cell behavior. The compound's specificity and effectiveness make it a top choice for researchers seeking compounds with strong therapeutic potential. Additionally, its consistent performance across different experimental conditions enhances its reliability in both academic and industrial research environments.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, Cediranib is commonly used by researchers specializing in cancer and cell biology. It supports studies aimed at understanding disease mechanisms and developing new therapeutic strategies. With the support of AMI Scientific, researchers can access high-quality materials necessary for accurate and reproducible experiments. Its presence in Indonesian research facilities highlights its importance in advancing cancer research and related biomedical fields.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eCancer Cell Proliferation Studies: Cediranib is used to investigate how it inhibits the growth of cancer cells, providing insights into potential therapeutic targets.\u003c\/li\u003e\n\u003cli\u003eMetastasis Research: The compound helps researchers understand the molecular pathways involved in cancer cell migration and spread.\u003c\/li\u003e\n\u003cli\u003eDrug Development Testing: Cediranib is employed in screening assays to evaluate its efficacy and mechanism of action in various cancer models.\u003c\/li\u003e\n\u003cli\u003eBiological Activity Assays: It is used to assess its impact on cell signaling pathways, making it valuable in studying cellular responses to targeted therapies.\u003c\/li\u003e\n\u003cli\u003ePreclinical Research: Cediranib supports the development of new cancer treatments by enabling the testing of its effects in controlled experimental conditions.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 288383-20-0\u003c\/li\u003e\n\u003cli\u003eCategory: Life Science \u0026gt; Cell Biology \u0026gt; Cancer Research\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per standard laboratory requirements\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from light\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eCediranib should be stored in a cool, dry environment, away from direct light and sources of heat. It is recommended to use airtight containers to prevent moisture absorption and contamination. Due to its chemical nature, it should be handled with appropriate personal protective equipment, such as gloves and safety goggles, to ensure laboratory safety. The compound is stable under standard storage conditions but should be kept in a secure location to prevent accidental exposure. Proper labeling of containers is essential to maintain safety and clarity in the laboratory setting. Regular monitoring of storage conditions ensures the integrity of the compound remains unaffected over time.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5mg","offer_id":48086302785754,"sku":"TCI2510C391819035","price":2559000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C3918.jpg?v=1769180464"},{"product_id":"tci2510c406119174","title":"TCI C4061 20575-57-9 Calycosin","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eCalycosin is a bioactive chemical compound widely used in life science research laboratories. It is derived from plant extracts and is valued for its diverse biological activities, including antioxidant and anti-inflammatory properties. This compound plays a crucial role in experimental studies aimed at understanding disease mechanisms, drug development, and plant metabolite research. Its presence in natural sources makes it an essential tool for researchers seeking to explore the pharmacological and biochemical properties of natural substances.\u003c\/p\u003e\n\u003cp\u003eCalycosin is preferred due to its chemical stability under controlled conditions, which simplifies storage and handling in laboratory settings. Its well-defined molecular structure allows for accurate analysis using various chemical and spectroscopic techniques. These characteristics make it a reliable choice for experiments requiring precision and reproducibility. Additionally, its consistent performance across different research applications enhances its utility in both academic and industrial research environments.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, Calycosin is commonly used in pharmacology, biochemistry, and health sciences research. It supports studies on natural compounds and their therapeutic potential. Many research institutions and universities in Indonesia incorporate Calycosin into their experimental protocols to advance scientific understanding and innovation in the field of natural product research.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003ePharmacological research utilizes Calycosin to investigate its potential therapeutic effects and mechanisms of action in drug development.\u003c\/li\u003e\n\u003cli\u003eBiochemical studies benefit from Calycosin’s antioxidant properties, enabling analysis of its role in cellular processes and oxidative stress.\u003c\/li\u003e\n\u003cli\u003ePlant metabolite research employs Calycosin to explore its natural occurrence and biochemical pathways in plant extracts.\u003c\/li\u003e\n\u003cli\u003eAnti-inflammatory studies leverage Calycosin’s biological activity to assess its impact on inflammatory responses and disease models.\u003c\/li\u003e\n\u003cli\u003eHealth sciences research incorporates Calycosin to examine its potential applications in natural medicine and therapeutic formulations.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 20575-57-9\u003c\/li\u003e\n\u003cli\u003eCategory: Life Science \u0026gt; Biochemicals and Reagents \u0026gt; Crude Medicine Ingredients for Research and Experimental Use\u003c\/li\u003e\n\u003cli\u003ePack sizes: As per supplier specifications\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid (as per standard product description)\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from direct sunlight\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eCalycosin should be stored in a cool, dry environment to maintain its chemical stability and prevent degradation. It is recommended to use airtight containers to minimize exposure to moisture and air, which can affect its integrity. Laboratory personnel should handle Calycosin with care, using appropriate personal protective equipment such as gloves and safety goggles. It is important to ensure that the compound is kept away from incompatible substances to avoid any chemical reactions. Proper labeling of storage containers is essential for safety and traceability. Regular monitoring of storage conditions ensures the compound remains suitable for research use.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"50mg","offer_id":48086318907610,"sku":"TCI2510C406119174","price":5116000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C4061.jpg?v=1767100479"},{"product_id":"tci2510c409919201","title":"TCI C4099 114289-47-3 CI 976","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C4099 114289-47-3 CI 976 is a chemical compound widely used in life science research, particularly in the field of cell biology and cancer research. This material serves as a key reagent in laboratory experiments aimed at studying the mechanisms of cancer cell growth and their response to therapeutic treatments. In the laboratory, it functions as an essential tool that supports the testing of biological activities, including toxicity and antitumor properties. Its presence enables researchers to conduct accurate and reliable experiments that contribute to the advancement of cancer research.\u003c\/p\u003e\n\u003cp\u003eThe compound is valued for its chemical stability and high purity, which ensure consistent results across repeated experiments. These properties make it a preferred choice for researchers who require reliable and reproducible data. Its resistance to degradation also simplifies storage and usage over extended periods, reducing the risk of experimental inconsistencies. Additionally, its high purity level ensures that it does not introduce unwanted variables into the experimental process, thereby enhancing the accuracy of research outcomes.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this compound is commonly used in cancer research conducted by academic institutions and research organizations. Scientists rely on it to develop new diagnostic methods and treatment strategies for cancer, as well as to gain deeper insights into the underlying mechanisms of the disease. Its application supports both basic and applied research, contributing to the broader scientific community’s understanding of cancer biology.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eAntitumor Activity Testing: This compound is ideal for assessing the effectiveness of potential cancer treatments on specific cell lines, providing critical data for drug development.\u003c\/li\u003e\n\u003cli\u003eChemical Toxicity Assessment: It supports experiments that evaluate the toxic effects of chemicals on cancer cells, helping to identify safe and effective therapeutic agents.\u003c\/li\u003e\n\u003cli\u003eCancer Cell Growth Studies: Researchers use it to investigate how cancer cells proliferate under various experimental conditions, aiding in the understanding of tumor progression.\u003c\/li\u003e\n\u003cli\u003eDevelopment of Cell Models: It facilitates the creation of reliable cell models that mimic human cancer, enabling more accurate and relevant research outcomes.\u003c\/li\u003e\n\u003cli\u003eDrug Screening and Validation: It is used in high-throughput screening processes to test the efficacy of new compounds against cancer cell lines, accelerating the discovery of novel therapies.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS Number: 114289-47-3\u003c\/li\u003e\n\u003cli\u003eCategory: Life Science \u0026gt; Cell Biology \u0026gt; Cancer Research\u003c\/li\u003e\n\u003cli\u003ePack Sizes: Not specified in the provided data\u003c\/li\u003e\n\u003cli\u003ePhysical Form: Not specified in the provided data\u003c\/li\u003e\n\u003cli\u003eStorage Note: Store in a cool, dry place away from direct sunlight\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis compound should be stored in a cool, dry environment to maintain its chemical stability and prevent degradation. It is recommended to use airtight containers to minimize exposure to moisture and air, which could affect its integrity. Due to its chemical properties, it should be handled with appropriate personal protective equipment, such as gloves and safety goggles, to ensure laboratory safety. Proper labeling of storage containers is essential for easy identification and safe handling. Regular monitoring of storage conditions is advised to ensure the material remains in optimal condition for use in research applications.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"20mg","offer_id":48086321758426,"sku":"TCI2510C409919201","price":3064000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C4099.jpg?v=1769144227"},{"product_id":"tci2510d004419339","title":"TCI D0044 53-43-0 Dehydroepiandrosterone","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eDehydroepiandrosterone (DHEA), with the CAS number 53-43-0, is a key organic compound widely used in laboratory research. As a pharmaceutical ingredient, it plays a crucial role in biochemical and pharmacological studies, particularly in the investigation of hormonal activity and metabolic processes. DHEA is commonly employed to explore the biological mechanisms of sex hormones such as testosterone and estrogen. Its presence in research settings allows scientists to study the physiological and biochemical effects of hormones on the human body.\u003c\/p\u003e\n\u003cp\u003eDHEA is valued for its chemical stability and solubility in organic solvents like ethyl acetate and acetone. These properties make it a reliable reagent for various experimental procedures. Its complex molecular structure also contributes to its popularity in scientific research, enabling detailed studies on hormone synthesis and metabolic pathways. The compound’s resistance to degradation under normal laboratory conditions ensures consistent results across experiments.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, DHEA is a vital component in health, pharmaceutical, and biomedical research. It is frequently used to investigate metabolic processes, pharmacological effects, and the development of new drugs. Researchers in Indonesia rely on DHEA to understand the mechanisms of hormone action and their impact on human physiology, supporting advancements in both academic and applied scientific fields.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eHormone Synthesis Studies: DHEA is used to investigate the biosynthesis of sex hormones, providing insights into metabolic pathways and hormonal regulation.\u003c\/li\u003e\n\u003cli\u003ePharmacological Research: It serves as a key reagent in studies evaluating the biological effects of hormones and their therapeutic potential.\u003c\/li\u003e\n\u003cli\u003eMetabolic Process Analysis: DHEA enables researchers to study how hormones influence metabolic functions and cellular activity in various biological systems.\u003c\/li\u003e\n\u003cli\u003eDrug Development: It is incorporated into the formulation and testing of new pharmaceutical compounds, supporting the development of hormone-based therapies.\u003c\/li\u003e\n\u003cli\u003eBiomedical Research: DHEA is utilized in experiments exploring the physiological and biochemical effects of hormones on human health and disease mechanisms.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS Number: 53-43-0\u003c\/li\u003e\n\u003cli\u003eCategory: Pharmaceutical Ingredients (for Research and Experimental Use)\u003c\/li\u003e\n\u003cli\u003ePack Sizes: As per supplier specifications\u003c\/li\u003e\n\u003cli\u003ePhysical Form: Solid\u003c\/li\u003e\n\u003cli\u003eStorage Note: Store in a cool, dry place away from light\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eDHEA should be stored in a cool, dry environment, away from direct light to maintain its chemical stability. It is recommended to use airtight containers to prevent moisture absorption and contamination. Due to its solubility in organic solvents, it should be handled in a well-ventilated area to minimize exposure. Researchers should wear appropriate personal protective equipment, such as gloves and safety goggles, when handling the compound. Proper labeling of containers is essential to ensure safe storage and use. Regular monitoring of storage conditions is advised to prevent degradation and maintain the integrity of the material for experimental use.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086335815898,"sku":"TCI2510D004419339","price":732000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086335848666,"sku":"TCI2510D004419340","price":1857000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48086335881434,"sku":"TCI2510D004419341","price":6437000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D0044.jpg?v=1767100714"},{"product_id":"tci2510d024219593","title":"TCI D0242 72-48-0 Alizarin","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eAlizarin TCI D0242, with CAS number 72-48-0, is a chemical compound widely used as a pigment in laboratory experiments. It is a key component in various analytical and experimental processes, particularly in the fields of chemistry, biology, and pharmacy. This compound is commonly employed for its ability to absorb and reflect specific wavelengths of light, making it an essential tool in staining and visualization techniques. Its presence in laboratory settings allows researchers to identify and analyze organic compounds effectively. Alizarin is also valuable in qualitative testing, where its reactivity with certain substances helps in determining the presence of specific ions or compounds.\u003c\/p\u003e\n\u003cp\u003eOne of the main reasons alizarin is preferred in laboratory applications is its stability under controlled conditions and its solubility in organic solvents. These properties make it suitable for a wide range of experimental setups, from basic research to advanced analytical procedures. Its ability to bind with other compounds enhances its utility in both qualitative and quantitative analysis. Additionally, alizarin’s consistent performance and reliability contribute to its popularity among scientists and researchers. Its physical form and chemical behavior make it a versatile reagent that can be adapted to various experimental needs.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, alizarin is frequently used in chemical, biological, and pharmaceutical research. It plays a crucial role in educational institutions and research facilities where staining and visualization techniques are required. Its availability in a 25-gram package makes it convenient for both small-scale experiments and larger research projects. Alizarin’s application in these settings highlights its importance as a fundamental reagent in the scientific community.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eAlizarin is used in chemical analysis for identifying organic compounds due to its distinct absorption and reflection properties.\u003c\/li\u003e\n\u003cli\u003eIt is commonly applied in biological research for staining and visualizing cellular structures, aiding in microscopic examination.\u003c\/li\u003e\n\u003cli\u003eAlizarin supports pharmaceutical studies by helping in the detection and analysis of specific compounds in drug formulations.\u003c\/li\u003e\n\u003cli\u003eIt is utilized in qualitative testing to detect the presence of certain ions or functional groups in a sample.\u003c\/li\u003e\n\u003cli\u003eAlizarin is employed in educational settings to demonstrate staining techniques and light interaction in chemistry and biology classes.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 72-48-0\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Stains and Dyes (for Research and Experimental Use) \u0026gt; Pigments (for Research and Experimental Use)\u003c\/li\u003e\n\u003cli\u003ePack sizes: 25 grams\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eAlizarin should be stored in a cool, dry place away from direct sunlight and moisture. It is recommended to keep it in a sealed container to prevent exposure to air and contaminants. Due to its chemical nature, it should be handled with care, using appropriate personal protective equipment such as gloves and safety goggles. Alizarin is not flammable but may react with strong oxidizing agents. It is important to ensure proper ventilation when working with this compound to avoid inhalation of any vapors. Storage in a well-ventilated area helps maintain its stability and effectiveness for laboratory use.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25g","offer_id":48086360883418,"sku":"TCI2510D024219593","price":1181000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D0242.jpg?v=1767101026"},{"product_id":"tci2510d191621896","title":"TCI D1916 38183-03-8 7,8-Dihydroxyflavone","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e7,8-Dihydroxyflavone is a flavonoid compound widely used in life science research due to its high biological activity. This compound plays a crucial role in biochemical and pharmacological studies, where it is employed as a building block for the synthesis of other compounds or as a testing agent. Its ability to interact with various biological pathways makes it an essential tool for researchers exploring the mechanisms of cellular processes. In the laboratory, it is frequently used to investigate the effects of flavonoids on cellular behavior and signaling.\u003c\/p\u003e\n\u003cp\u003eOne of the key properties that make 7,8-Dihydroxyflavone a preferred choice is its complex chemical structure and ability to cross cell membranes. These characteristics enable it to be effectively used in studies involving cellular uptake and bioavailability. Additionally, its solubility in organic solvents such as ethyl acetate and ethanol facilitates its use in analytical and preparative procedures. This solubility profile is particularly advantageous for chromatographic and spectroscopic analyses, ensuring accurate and reproducible results.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, 7,8-Dihydroxyflavone is commonly utilized in applied research areas such as pharmacology, biochemistry, and neuroscience. Its relevance extends to studies examining the biological effects of flavonoids, especially in the context of antioxidant, antidepressant, and anti-inflammatory activities. Its versatility and reliability make it a go-to compound for researchers seeking precise and consistent results in their experiments.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003ePharmacological research benefits from 7,8-Dihydroxyflavone’s ability to interact with various biological pathways, making it ideal for studying drug mechanisms and therapeutic effects.\u003c\/li\u003e\n\u003cli\u003eBiochemical studies often use this compound to investigate its role in cellular signaling and metabolic processes due to its structural complexity and biological activity.\u003c\/li\u003e\n\u003cli\u003eNeuroscientific research leverages its potential in studying neuroprotective effects and its interaction with neurotransmitter systems, supporting studies on brain function.\u003c\/li\u003e\n\u003cli\u003eAntioxidant research utilizes 7,8-Dihydroxyflavone to assess its capacity to neutralize free radicals and protect cellular components from oxidative damage.\u003c\/li\u003e\n\u003cli\u003eAnti-inflammatory studies benefit from its ability to modulate inflammatory responses, making it a valuable tool in investigating the mechanisms of inflammation and disease progression.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 38183-03-8\u003c\/li\u003e\n\u003cli\u003eCategory: Life Science \u0026gt; Biochemicals and Reagents \u0026gt; Phenylpropanoids, Aromatic Polyketides\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per standard laboratory requirements\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid powder\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from light and moisture\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003e7,8-Dihydroxyflavone should be stored in a cool, dry environment, away from direct light and moisture to maintain its chemical integrity. It is recommended to use airtight containers to prevent exposure to humidity and potential degradation. In laboratory settings, proper personal protective equipment such as gloves and safety goggles should be worn when handling this compound to ensure safety. Due to its solubility in organic solvents, it is important to handle it in well-ventilated areas to avoid inhalation of vapors. The compound should be kept in a secure location to prevent accidental spills or contamination. Regular monitoring of storage conditions is advised to ensure the compound remains stable and suitable for use in research applications.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086483206362,"sku":"TCI2510D191621896","price":1743000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086483239130,"sku":"TCI2510D191621897","price":5481000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D1916.jpg?v=1771058115"},{"product_id":"tci2510d337123627","title":"TCI D3371 15663-27-1 cis-Diammineplatinum(II) Dichloride","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003ecis-Diammineplatinum(II) Dichloride is a chemical compound widely used in catalytic reactions and organic synthesis within laboratory settings. As a transition metal complex, it exhibits unique reactivity and structural properties that make it valuable for various chemical processes. This compound is particularly useful in reactions requiring electronic activation or molecular structure modification. Its role as a catalyst is essential in advancing research in inorganic chemistry and catalysis, where precise control over reaction pathways is crucial.\u003c\/p\u003e\n\u003cp\u003eThe compound's stability and reactivity are key factors that make it a preferred choice in laboratory applications. It has the ability to form metal complexes with a variety of ligands, which enhances its versatility in different chemical environments. Its chiral structure also makes it significant in the study of reaction mechanisms and asymmetric synthesis. These properties allow researchers to explore complex molecular transformations with greater precision and control.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, cis-Diammineplatinum(II) Dichloride is commonly used in academic and research institutions. It plays a vital role in chemical research, especially in areas such as catalytic processes and inorganic chemistry. Its availability and reliability make it a standard material for experiments requiring high chemical specificity and controlled reactivity. This compound supports a wide range of scientific investigations, contributing to the advancement of chemical knowledge in the region.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eCatalytic Reactions: This compound is ideal for catalytic processes due to its ability to activate electron transfer and facilitate molecular rearrangements.\u003c\/li\u003e\n\u003cli\u003eAsymmetric Synthesis: Its chiral structure makes it suitable for studying asymmetric reactions and the formation of enantiomers in organic chemistry.\u003c\/li\u003e\n\u003cli\u003eInorganic Chemistry Research: It is widely used in the study of transition metal complexes and their interactions with various ligands.\u003c\/li\u003e\n\u003cli\u003eStructural Modification Studies: The compound is valuable for experiments involving molecular structure changes and electronic activation.\u003c\/li\u003e\n\u003cli\u003eMetal Complex Formation: Its reactivity allows it to form stable complexes with different ligands, making it useful in coordination chemistry research.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 15663-27-1\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Catalysis and Inorganic Chemistry \u0026gt; Transition Elements\u003c\/li\u003e\n\u003cli\u003ePack sizes: Not specified\u003c\/li\u003e\n\u003cli\u003ePhysical form: Not specified\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from moisture and light\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis compound should be stored in a cool, dry place, away from moisture and direct light. It is recommended to use airtight containers to prevent exposure to air and humidity. Due to its chemical reactivity, it should be handled with care, using appropriate personal protective equipment such as gloves and safety goggles. Avoid contact with incompatible substances to ensure safe storage and usage. Regular monitoring of storage conditions is advised to maintain the compound’s stability and effectiveness in laboratory applications.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"100mg","offer_id":48086610837722,"sku":"TCI2510D337123627","price":1575000.0,"currency_code":"IDR","in_stock":true},{"title":"1g","offer_id":48086610870490,"sku":"TCI2510D337123628","price":7308000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D3371.jpg?v=1767106003"},{"product_id":"tci2510d357923895","title":"TCI D3579 3094-09-5 5'-Deoxy-5-fluorouridine","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI D3579 5'-Deoxy-5-fluorouridine, widely known as doxifluridine or 5'-DFUR, is a synthetic fluoropyrimidine nucleoside that holds an important position as a reference material in biochemistry and pharmacology laboratories. The compound is a uridine derivative that lacks the hydroxyl group at the 5' position and carries a fluorine atom at position 5 of the pyrimidine ring. This distinctive structure makes it a classic prodrug studied intensively in antimetabolite metabolism research, because its conversion into the active form depends on thymidine phosphorylase activity within tissues. In the laboratory, this material serves as a test compound, an analytical standard, and a starting material for mechanistic studies of fluoropyrimidine-based drugs.\u003c\/p\u003e\n\u003cp\u003eThe characteristics that lead many researchers to select 5'-Deoxy-5-fluorouridine are the combination of reasonable storage stability in solid form and highly specific biological reactivity once it is enzymatically activated. The presence of the fluorine atom at position 5 gives the molecule electronic properties different from those of natural uracil, allowing the compound to interfere with the thymidylate synthesis pathway after conversion. Its well-defined structure and consistent behaviour as a nucleoside derivative make it suitable for use as a comparison compound, so that experimental results obtained in different laboratories remain interpretable against a common reference point.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this material is typically used in university research groups, pharmacology and biochemistry teaching laboratories, and pharmaceutical research units that study antimetabolite mechanisms. It is commonly employed in enzyme activity assays, cell-based studies, and analytical method development where a defined fluoropyrimidine nucleoside is required. Because it is supplied by TCI as a catalogue chemical, it fits routine research workflows in which reproducibility and traceable identity of the compound matter as much as the experiment itself.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eProdrug activation studies — the compound depends on thymidine phosphorylase for conversion, making it a direct model for investigating tissue-dependent enzymatic activation of nucleoside prodrugs in controlled experiments.\u003c\/li\u003e\n\u003cli\u003eAntimetabolite mechanism research — because the activated form interferes with the thymidylate synthesis pathway, it allows researchers to trace how fluoropyrimidines disrupt nucleotide biosynthesis at the biochemical level.\u003c\/li\u003e\n\u003cli\u003eAnalytical standard preparation — its defined identity as a fluoropyrimidine nucleoside makes it suitable as a reference substance for chromatographic and spectroscopic method development and system suitability checks.\u003c\/li\u003e\n\u003cli\u003eEnzyme activity assays — thymidine phosphorylase studies can use this substrate to compare conversion rates between sample types, since the enzymatic dependency of the molecule is well characterised.\u003c\/li\u003e\n\u003cli\u003eStructure–activity relationship studies — the 5'-deoxy modification and 5-fluoro substitution provide a defined structural template for comparing uridine derivatives and evaluating how each modification changes biological behaviour.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI (Tokyo Chemical Industry)\u003c\/li\u003e\n\u003cli\u003eCAS Number: 3094-09-5\u003c\/li\u003e\n\u003cli\u003eCatalogue Number: D3579\u003c\/li\u003e\n\u003cli\u003eCategory: Life Science \u0026gt; Biochemicals and Reagents \u0026gt; Nucleosides, Nucleotides, Oligonucleotides\u003c\/li\u003e\n\u003cli\u003eChemical Class: Synthetic fluoropyrimidine nucleoside, uridine derivative (doxifluridine \/ 5'-DFUR)\u003c\/li\u003e\n\u003cli\u003ePack Sizes: Available in standard TCI research-scale packaging; please confirm the size required when ordering\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eStore the material in its original tightly closed container, kept in a cool, dry place and protected from light and moisture, following the storage conditions stated on the manufacturer's label and safety data sheet. Amber glass or the supplied original packaging is appropriate, and containers should be resealed promptly after each use to limit exposure to humid air. Handle the solid in a well-ventilated area or fume hood, wearing a laboratory coat, nitrile gloves, and eye protection, and avoid generating dust during weighing or transfer. As a biologically active fluoropyrimidine compound intended for research use only, it should be handled by trained personnel, kept away from food and drink, and disposed of as chemical waste in accordance with institutional and local regulations. Consult the manufacturer's safety data sheet before first use.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086627516634,"sku":"TCI2510D357923895","price":2222000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086627549402,"sku":"TCI2510D357923896","price":6634000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D3579.jpg?v=1769180615"},{"product_id":"tci2510d358023897","title":"TCI D3580 3056-17-5 2',3'-Didehydro-3'-deoxythymidine","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI D3580 2',3'-Didehydro-3'-deoxythymidine, more widely known as stavudine or d4T, is a thymidine nucleoside analogue that has become one of the most important reference compounds in molecular virology research. The molecule is characterised by a double bond between the 2' and 3' positions of the sugar ring together with the absence of a hydroxyl group at the 3' position. It is precisely this missing 3'-OH group that gives the compound its chain-terminating behaviour once the triphosphate form is incorporated by reverse transcriptase. In the laboratory, the material is used as an antiviral test compound, as an analytical standard for method development, and as a structural model in the design of next-generation nucleoside analogues.\u003c\/p\u003e\n\u003cp\u003eThe property that makes this compound such a frequent choice is the clarity of its mechanism of action, which is very well established in the published literature, so that experimental results can be compared easily against existing reference data. The didehydro-dideoxy modification on the sugar imparts a particular conformational rigidity that influences recognition by cellular kinases as well as by viral polymerases. As a solid, the compound is relatively straightforward to weigh out and to dissolve in the solvents commonly used for biological assays. Lot-to-lot consistency in purity from TCI supports reproducible work across repeated experiments.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this material is typically found in university research groups, biomedical and pharmaceutical research institutes, and analytical method development laboratories working on antiviral chemistry. It is generally handled at small scale for assay work, comparative studies against newer nucleoside analogues, and as a reference substance when calibrating or validating chromatographic methods. Its well-documented behaviour makes it a practical teaching and benchmarking material for research teams building capability in molecular virology.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eAntiviral assay reference compound — the well-characterised chain-termination mechanism allows researchers to benchmark new candidate molecules against a compound whose behaviour is already fully documented.\u003c\/li\u003e\n\u003cli\u003eAnalytical method development and validation — the material serves as a reference substance when establishing chromatographic or spectroscopic procedures that must resolve and quantify nucleoside analogues reliably.\u003c\/li\u003e\n\u003cli\u003eReverse transcriptase mechanism studies — the absent 3'-hydroxyl group makes this compound a clear model for demonstrating and probing how chain termination occurs during viral DNA synthesis.\u003c\/li\u003e\n\u003cli\u003eNucleoside analogue design work — the didehydro-dideoxy sugar modification provides a structural template that medicinal chemists use when planning conformationally constrained analogues for further evaluation.\u003c\/li\u003e\n\u003cli\u003eEnzyme recognition and phosphorylation studies — the conformational rigidity of the sugar ring makes the molecule useful for examining how cellular kinases and viral polymerases discriminate between substrates.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS Number: 3056-17-5\u003c\/li\u003e\n\u003cli\u003eCatalogue Number: D3580\u003c\/li\u003e\n\u003cli\u003eCategory: Life Science \u0026gt; Biochemicals and Reagents \u0026gt; Antibiotics\u003c\/li\u003e\n\u003cli\u003ePhysical form: solid\u003c\/li\u003e\n\u003cli\u003ePack sizes: available in the standard TCI catalogue pack sizes; please refer to the product listing for the options currently offered\u003c\/li\u003e\n\u003cli\u003eStorage: store according to the conditions stated on the manufacturer's label and product documentation\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eStore the container tightly closed in a cool, dry place away from direct sunlight, moisture, and incompatible materials, following the storage conditions given on the manufacturer's label and safety data sheet. Keep the material in its original container or in a clean, chemically resistant, well-sealed vessel that is clearly labelled. Handle the solid in a well-ventilated area or fume hood, using gloves, safety glasses, and a laboratory coat, and avoid generating dust during weighing. Allow the container to reach room temperature before opening if it has been kept refrigerated, in order to limit condensation. Consult the safety data sheet before use and dispose of residues and contaminated consumables in accordance with applicable laboratory waste procedures.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086627614938,"sku":"TCI2510D358023897","price":1687000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086627647706,"sku":"TCI2510D358023898","price":5369000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D3580.jpg?v=1767106266"},{"product_id":"tci2510d363423977","title":"TCI D3634 4342-03-4 Dacarbazine","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI D3634 Dacarbazine is a triazene compound linked to a carboxamide-substituted imidazole ring, known as an antineoplastic agent belonging to the alkylating class. This product is categorized as a pharmaceutical research reagent for experimental use, so its role in the laboratory is that of a reference reagent in pharmacological studies, experimental oncology, and analytical method development. In research settings, this compound is commonly used as a comparator for assessing cellular responses to alkylating agents, as well as a working standard in the establishment and validation of assay methods for content determination. This product is not intended for diagnostic or therapeutic use in humans.\u003c\/p\u003e\n\u003cp\u003eThe characteristic that makes this compound important in research is its mechanism of action as a precursor that must first be activated. The dimethyltriazene group on the molecule can decompose to generate alkylating species that react with nucleic acid bases, which is why the compound is frequently used to study DNA damage and the cellular mechanisms that repair it. Another property that must be taken into account is its sensitivity to light and heat; triazene compounds tend to decompose upon exposure to light, so protection from illumination and controlled temperature handling are essential to preserving the integrity of the material throughout an experiment.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this reagent is typically encountered in university research groups, pharmacy and life science faculties, and analytical laboratories that develop or verify quantitative methods. It generally serves as a reference point in cell-based experiments and in chromatographic assay work, where a well-defined alkylating agent is required for comparison. Because it is supplied strictly for experimental purposes, its use is confined to research protocols rather than clinical or diagnostic procedures.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eCytotoxicity and cell response studies: serves as a comparator alkylating agent so researchers can benchmark how cultured cells respond relative to a well-characterized reference compound.\u003c\/li\u003e\n\u003cli\u003eDNA damage research: the dimethyltriazene group decomposes into alkylating species that react with nucleic acid bases, making it suitable for investigating induced DNA lesions.\u003c\/li\u003e\n\u003cli\u003eDNA repair mechanism investigations: because the alkylation event is defined and reproducible, it allows the cellular repair pathways responding to that damage to be traced and characterized.\u003c\/li\u003e\n\u003cli\u003eAnalytical method development and validation: functions as a working standard when assay procedures for content determination are being established, optimized, and verified for reliability.\u003c\/li\u003e\n\u003cli\u003eExperimental oncology and pharmacology research: acts as a reference antineoplastic agent for studies examining the pharmacological behaviour of alkylating-class compounds under controlled laboratory conditions.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS Number: 4342-03-4\u003c\/li\u003e\n\u003cli\u003eCategory: Life Science \u0026gt; Biochemicals and Reagents \u0026gt; Pharmaceutical Research Reagents (for Experimental Use)\u003c\/li\u003e\n\u003cli\u003eProduct Code: D3634\u003c\/li\u003e\n\u003cli\u003eIntended Use: experimental and research use only; not for diagnostic or therapeutic application in humans\u003c\/li\u003e\n\u003cli\u003eStorage Note: protect from light and store under controlled temperature conditions, as triazene compounds are sensitive to light and heat\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eStore this reagent in its original tightly closed container, protected from light and kept under controlled temperature conditions, since triazene compounds are prone to decomposition when exposed to illumination or heat. Amber glass or light-shielded containers are appropriate for aliquots and prepared solutions, and containers should be clearly labelled and dated. Handle the material in a well-ventilated area or fume hood using standard personal protective equipment, including gloves, a laboratory coat, and eye protection, and avoid the generation of dust. As an antineoplastic alkylating compound, it should be handled by trained personnel following the institution's laboratory safety procedures for cytotoxic substances, with waste collected and disposed of according to applicable regulations.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086630662362,"sku":"TCI2510D363423977","price":2222000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086630695130,"sku":"TCI2510D363423978","price":6437000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D3634.jpg?v=1769180618"},{"product_id":"tci2510d398624435","title":"TCI D3986 478-43-3 4,5-Dihydroxyanthraquinone-2-carboxylic Acid","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI D3986 4,5-Dihydroxyanthraquinone-2-carboxylic Acid (CAS 478-43-3), widely known among researchers as rhein, is a hydroxylated anthraquinone derivative that carries a carboxylic acid group on its tricyclic framework. In the laboratory this material plays a dual role: it serves as a non-heterocyclic building block for organic synthesis, and at the same time it functions as a reference compound in natural product research, particularly in studies of secondary metabolites of the anthraquinone class that are commonly found in plants of the Polygonaceae and Fabaceae families. Its presence helps researchers establish the identity of isolated compounds with greater confidence.\u003c\/p\u003e\n\u003cp\u003eThe characteristic that makes this material a frequent choice is its combination of functional groups that is rich yet still manageable: two phenolic hydroxyl groups that are weakly acidic and capable of forming intramolecular hydrogen bonds with the quinone carbonyl groups, plus a single carboxylic acid group that provides a clear derivatisation point for both esterification and amidation. The anthraquinone framework supplies a strongly conjugated chromophore system, so the compound is easily monitored with a UV-Vis detector in HPLC as well as by spectrophotometric scanning. This makes it convenient to track through reaction sequences and analytical workflows alike.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this profile fits the work routinely carried out in university natural product groups, pharmacy and pharmacognosy laboratories, and chemical synthesis laboratories. It is used as a comparison standard when confirming anthraquinone metabolites isolated from local plant material, and as a starting scaffold when researchers need to prepare derivatives around the anthraquinone core. Because it is detected readily by common UV-Vis instrumentation, it integrates well with the analytical equipment already available in most institutional laboratories.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eNatural product reference compound — used as a comparison marker so anthraquinone metabolites isolated from Polygonaceae and Fabaceae plant material can be identified with greater confidence.\u003c\/li\u003e\n\u003cli\u003eNon-heterocyclic building block for organic synthesis — the intact anthraquinone framework serves as a starting scaffold for researchers preparing structurally related target compounds.\u003c\/li\u003e\n\u003cli\u003eCarboxyl-directed derivatisation chemistry — the single carboxylic acid group provides a clear and well-defined point of attachment for esterification and amidation reactions.\u003c\/li\u003e\n\u003cli\u003eHPLC method development and analysis — the strongly conjugated anthraquinone chromophore is readily monitored with a UV-Vis detector, making the compound convenient for chromatographic work.\u003c\/li\u003e\n\u003cli\u003eUV-Vis spectrophotometric studies — the same conjugated chromophore system allows straightforward spectrophotometric scanning, supporting characterisation work and routine verification of isolated fractions.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS Number: 478-43-3\u003c\/li\u003e\n\u003cli\u003eChemical name: 4,5-Dihydroxyanthraquinone-2-carboxylic Acid (also known as rhein)\u003c\/li\u003e\n\u003cli\u003eProduct code: D3986\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Non-Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: available in standard TCI research-scale packaging; please refer to the current catalogue listing for available options\u003c\/li\u003e\n\u003cli\u003eStorage: store according to the storage conditions stated on the product label and in the accompanying documentation\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eStore the container tightly closed in a cool, dry, well-ventilated place, away from direct sunlight and sources of heat or ignition, and follow the specific storage conditions indicated on the product label and Safety Data Sheet. Keep the material in its original supplier container, or in a chemically compatible, clearly labelled amber glass container if transfer is necessary, since the conjugated chromophore makes light protection sensible. Handle in a fume hood using standard personal protective equipment — safety goggles, gloves, and a laboratory coat — and avoid the generation and inhalation of dust when weighing the solid. Wash hands thoroughly after handling, keep the container closed when not in use, and dispose of residues and contaminated materials in accordance with applicable laboratory and institutional waste procedures. Always consult the Safety Data Sheet before first use.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"200mg","offer_id":48086649602266,"sku":"TCI2510D398624435","price":4414000.0,"currency_code":"IDR","in_stock":true},{"title":"1g","offer_id":48086649635034,"sku":"TCI2510D398624436","price":14418000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D3986.jpg?v=1767106898"},{"product_id":"tci2510d410224588","title":"TCI D4102 114977-28-5 Docetaxel","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI D4102 Docetaxel, CAS 114977-28-5, is a taxane-class compound widely recognised as an antimitotic agent. In research laboratories, docetaxel serves as a reference compound and pharmacological tool for studying microtubule dynamics, the cell cycle, and the mechanisms of programmed cell death. The material stabilises microtubules and inhibits their normal depolymerisation, causing cells to arrest at a particular stage of division. Because of its strong and well-defined biological effect, this compound is frequently employed as a positive control in cytotoxicity assays and in the screening of new candidate anticancer compounds.\u003c\/p\u003e\n\u003cp\u003eThe properties that make docetaxel a preferred choice are its high potency at low concentrations and its specific mechanism of action on microtubules, which makes experimental results easier to interpret than those obtained with compounds acting on multiple targets. This material is supplied as a solid and is generally dissolved in an organic solvent such as dimethyl sulfoxide to prepare a stock solution, which is then diluted into culture medium. Its limited solubility in water requires careful attention during solution preparation so that precipitation does not occur.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this compound is typically used in academic research units, pharmacology and biomedical laboratories, and cell culture facilities working on anticancer screening. It is normally handled in small quantities from a concentrated stock solution, with dilution steps carried out immediately before an assay. As a cytotoxic compound, docetaxel is handled under controlled conditions, with work planned so that exposure is kept to a minimum and the material remains confined to a designated working area.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eMicrotubule dynamics studies — the compound stabilises microtubules and blocks normal depolymerisation, giving researchers a reliable and reproducible way to perturb the cytoskeleton.\u003c\/li\u003e\n\u003cli\u003eCell cycle analysis — because it arrests dividing cells at a defined stage, it provides a clear and consistent reference point when examining progression through the cell cycle.\u003c\/li\u003e\n\u003cli\u003eApoptosis and programmed cell death research — its strong, well-characterised biological effect makes it suitable for investigating the mechanisms that lead cells toward programmed death.\u003c\/li\u003e\n\u003cli\u003ePositive control in cytotoxicity assays — its potency at low concentrations and well-defined response make it a dependable benchmark against which test samples can be compared.\u003c\/li\u003e\n\u003cli\u003eScreening of new anticancer candidate compounds — its specific action on microtubules rather than multiple targets allows results from screening campaigns to be interpreted with greater confidence.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 114977-28-5\u003c\/li\u003e\n\u003cli\u003eCategory: Life Science \u0026gt; Biochemicals and Reagents \u0026gt; Antibiotics\u003c\/li\u003e\n\u003cli\u003eCatalogue number: D4102\u003c\/li\u003e\n\u003cli\u003ePhysical form: solid; generally dissolved in an organic solvent such as dimethyl sulfoxide to prepare stock solutions\u003c\/li\u003e\n\u003cli\u003eStorage: store according to the conditions stated on the manufacturer's label and accompanying documentation\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eStore the container closed and stored in accordance with the conditions indicated on the manufacturer's label and product documentation. Keep the solid in its original tightly sealed container, protected from moisture, and use containers compatible with organic solvents when preparing and holding stock solutions. Because docetaxel is a cytotoxic compound, handle it with appropriate personal protective equipment, including gloves, a laboratory coat, and eye protection, and carry out weighing and solution preparation in a suitable containment enclosure. Prepare dilutions carefully to avoid precipitation given its limited solubility in water, label all stock solutions clearly, and dispose of residues and contaminated consumables through the laboratory's designated route for cytotoxic waste.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"100mg","offer_id":48086655566042,"sku":"TCI2510D410224588","price":3121000.0,"currency_code":"IDR","in_stock":true},{"title":"1g","offer_id":48086655598810,"sku":"TCI2510D410224589","price":14727000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D4102.jpg?v=1767107071"},{"product_id":"tci2510d414824655","title":"TCI D4148 32981-86-5 10-Deacetylbaccatin III","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI D4148 10-Deacetylbaccatin III is a natural product belonging to the taxane class of diterpenoids, obtained naturally from plants of the genus *Taxus*, commonly known as the yew tree. The compound is widely recognized as the core scaffold that serves as the starting point for taxane chemistry, one of the most important classes of molecules in the history of modern drug discovery. In the laboratory, this material is used primarily as a semi-synthetic precursor, an analytical reference standard, and a subject of study in natural product research. Its availability in isolated form saves researchers the long extraction and purification stages that would otherwise be required.\u003c\/p\u003e\n\u003cp\u003eThe characteristic that makes this compound valuable is its polycyclic taxane skeleton, which carries an arrangement of hydroxyl and ester groups already established in the correct stereochemical configuration. Such an intricate structure is almost impossible to construct efficiently through total synthesis, so its use as a semi-synthetic starting material offers a substantial advantage. The hydroxyl groups differ in their degree of reactivity, which allows selective modification through stepwise protection, acylation, and side-chain coupling. Researchers can therefore generate a range of taxane analogues in order to study structure-activity relationships.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this material is typically handled in university research groups, natural product chemistry laboratories, pharmaceutical development units, and analytical service laboratories. It supports work in which a well-defined taxane scaffold is required either as a synthetic building block or as a comparison standard for identification and method development. Because the isolated compound removes the need for in-house extraction from plant material, it allows research teams to focus their resources directly on synthesis, characterization, and analytical work.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eSemi-synthetic precursor work: the pre-formed taxane skeleton with its established stereochemistry lets chemists build taxane derivatives without attempting the impractical route of total synthesis.\u003c\/li\u003e\n\u003cli\u003eAnalytical reference standard: a defined, isolated taxane compound provides a reliable comparison point for identification, peak confirmation, and analytical method development in chromatographic and spectroscopic work.\u003c\/li\u003e\n\u003cli\u003eNatural product chemistry research: as a characteristic constituent of *Taxus* species, the compound serves as a study object for investigating taxane biosynthesis, isolation strategies, and natural product structure.\u003c\/li\u003e\n\u003cli\u003eStructure-activity relationship studies: the differing reactivity of its hydroxyl groups permits selective protection, acylation, and side-chain attachment, enabling the preparation of taxane analogue series for comparison.\u003c\/li\u003e\n\u003cli\u003eSelective derivatization and protecting-group methodology: the multiple hydroxyl functions on a complex scaffold make this material a practical substrate for developing and validating stepwise protection and acylation procedures.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 32981-86-5\u003c\/li\u003e\n\u003cli\u003eCategory: Life Science \u0026gt; Biochemicals and Reagents \u0026gt; Antibiotics\u003c\/li\u003e\n\u003cli\u003eProduct code: D4148\u003c\/li\u003e\n\u003cli\u003ePack sizes: available in standard research and laboratory pack sizes as offered by the manufacturer\u003c\/li\u003e\n\u003cli\u003eStorage: store according to the conditions stated on the manufacturer label and product documentation\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eStore the container in a cool, dry place, protected from light and moisture, and follow the storage conditions stated on the manufacturer label and accompanying documentation. Keep the material in its original tightly closed container, or in a suitable amber glass or chemically resistant vessel that is clearly labelled with the compound name and product code. Handle the compound in a well-ventilated area or fume hood, and wear appropriate personal protective equipment including gloves, safety glasses, and a laboratory coat. Avoid the generation of dust, avoid contact with skin and eyes, and use clean, dry spatulas and glassware when weighing to prevent contamination. Return the container promptly to its designated storage location after use, and consult the safety data sheet before opening, handling, or disposing of the material.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"100mg","offer_id":48086657990874,"sku":"TCI2510D414824655","price":1941000.0,"currency_code":"IDR","in_stock":true},{"title":"500mg","offer_id":48086658023642,"sku":"TCI2510D414824656","price":6156000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D4148.jpg?v=1767107144"},{"product_id":"tci2510d419324714","title":"TCI D4193 25316-40-9 Doxorubicin Hydrochloride","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI D4193 Doxorubicin Hydrochloride, bearing CAS number 25316-40-9, is an anthracycline compound supplied in its hydrochloride salt form and classified within chemical biology, specifically the field of glycoscience, because its structure contains an amino sugar moiety attached to a polyketide aglycone core. It is one of the most widely recognised reagents in cell biology research and experimental oncology, employed as a comparative treatment in cell viability assays, DNA damage studies, and drug resistance research. Its established role as a reference compound makes it an important part of the modern biomedical research laboratory toolkit.\u003c\/p\u003e\n\u003cp\u003eThe characteristics that make doxorubicin such a frequently chosen compound include its ability to intercalate between DNA base pairs and its influence on the activity of the topoisomerase II enzyme, two properties that together produce clear and readily observable cellular responses. The molecule is also intrinsically fluorescent, so its uptake into cells can be monitored directly by fluorescence microscopy or flow cytometry without the need for any additional labelling step. The daunosamine sugar portion improves solubility in water, and the hydrochloride salt form makes the preparation of aqueous stock solutions straightforward and practical for routine bench work.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this reagent is typically found in university research groups, biomedical and pharmaceutical research institutes, and cell culture facilities working on oncology-related questions. It commonly serves as the positive control or benchmark treatment in cytotoxicity screening panels, where new candidate compounds are compared against a well-characterised standard. Because its behaviour in cell-based systems is thoroughly documented, it also supports method development, assay validation, and the training of researchers and postgraduate students in cell biology techniques.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eCell viability and cytotoxicity assays, where it functions as a reliable comparative treatment against which the activity of newly synthesised or extracted candidate compounds can be measured.\u003c\/li\u003e\n\u003cli\u003eDNA damage studies, since its intercalation between DNA base pairs and its effect on topoisomerase II activity generate clear, reproducible cellular responses suitable for mechanistic investigation.\u003c\/li\u003e\n\u003cli\u003eDrug resistance research, in which it is used as a reference anthracycline to characterise resistant cell populations and to examine how treatment responses shift across experimental conditions.\u003c\/li\u003e\n\u003cli\u003eCellular uptake and localisation experiments, taking advantage of its intrinsic fluorescence so that entry into cells can be tracked by fluorescence microscopy without adding any external label.\u003c\/li\u003e\n\u003cli\u003eFlow cytometry workflows in experimental oncology, where the compound's own fluorescent signal allows quantitative assessment of accumulation across cell populations without an additional staining procedure.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS Number: 25316-40-9\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Chemical Biology \u0026gt; Glycoscience\u003c\/li\u003e\n\u003cli\u003eChemical class: anthracycline compound supplied as the hydrochloride salt\u003c\/li\u003e\n\u003cli\u003eSolubility note: the daunosamine sugar moiety supports water solubility, and the hydrochloride salt form facilitates preparation of aqueous stock solutions\u003c\/li\u003e\n\u003cli\u003ePack sizes: available in the pack sizes listed on the product page; please confirm the option required when ordering\u003c\/li\u003e\n\u003cli\u003eStorage: store according to the conditions stated on the manufacturer's label and product documentation\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eStore this product under the conditions specified on the manufacturer's label and accompanying documentation, keeping the container tightly closed and protected from light, moisture, and elevated temperature. Use clean, chemically compatible containers for aqueous stock solutions, label them clearly with concentration and preparation date, and aliquot where repeated freeze-thaw cycles would otherwise be required. Handle the material only in a designated laboratory area using appropriate personal protective equipment, including gloves, a laboratory coat, and eye protection, and carry out weighing and solution preparation with suitable engineering controls in place. Avoid the generation of dust or aerosols, keep the compound away from incompatible materials, and dispose of residues and contaminated consumables through the established chemical waste procedures of your institution. Always consult the Safety Data Sheet before first use.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25mg","offer_id":48086677881050,"sku":"TCI2510D419324714","price":6409000.0,"currency_code":"IDR","in_stock":true},{"title":"100mg","offer_id":48086677913818,"sku":"TCI2510D419324715","price":19169000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D4193.jpg?v=1767107201"},{"product_id":"tci2510d429224848","title":"TCI D4292 53-85-0 5,6-Dichlorobenzimidazole 1-beta-D-Ribofuranoside","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI D4292 is 5,6-Dichlorobenzimidazole 1-beta-D-Ribofuranoside, a nucleoside analogue that combines a chlorinated benzimidazole base with a ribofuranose sugar in the beta configuration. The compound is widely known among molecular biology researchers as a reagent for interfering with transcription in cells, and it is commonly abbreviated as DRB in the literature. As a material in the biochemicals and reagents category, this product is intended for cell-based experiments and gene expression analysis rather than for large-scale chemical synthesis work.\u003c\/p\u003e\n\u003cp\u003eThe feature that makes this compound a preferred choice is its ability to enter cells and act as an inhibitor of the kinase associated with RNA chain elongation by RNA polymerase II, so that its effect on transcription can be observed within a relatively short time frame and is reversible once the reagent is washed out. Its nucleoside structure gives it reasonable solubility in polar organic solvents such as dimethyl sulfoxide, making it straightforward to prepare as a concentrated stock solution that is then diluted into culture medium. The presence of two chlorine atoms on the benzimidazole ring adds lipophilic character that assists cell membrane penetration compared with more polar nucleosides.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this reagent is typically used in molecular biology and cell biology settings where transcription needs to be modulated under controlled conditions. It is handled at the bench scale of cell culture and gene expression work, prepared as a stock solution in a polar organic solvent and then applied to culture medium at working concentrations. Its rapid and reversible action suits experimental designs that compare cells before, during, and after treatment within a single working session.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eTranscription inhibition studies: the compound enters cells readily and interferes with the transcription process, allowing researchers to establish a defined transcriptional shutdown point in cultured cells.\u003c\/li\u003e\n\u003cli\u003eRNA polymerase II elongation research: because it inhibits the kinase associated with RNA chain elongation by RNA polymerase II, it is well suited to work examining the elongation phase specifically rather than general transcription.\u003c\/li\u003e\n\u003cli\u003eGene expression analysis: the reagent supports experiments where transcript levels must be measured following a controlled interruption of transcription, making expression changes easier to interpret over time.\u003c\/li\u003e\n\u003cli\u003eReversible treatment experiments: its effect can be reversed after the reagent is washed out, which suits designs comparing treated and recovered cell populations within the same experimental series.\u003c\/li\u003e\n\u003cli\u003eCell-based reagent screening: its lipophilic chlorinated benzimidazole ring assists membrane penetration, so it performs well in live-cell assays that require the compound to reach intracellular targets quickly.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS Number: 53-85-0\u003c\/li\u003e\n\u003cli\u003eChemical name: 5,6-Dichlorobenzimidazole 1-beta-D-Ribofuranoside\u003c\/li\u003e\n\u003cli\u003eCategory: Life Science \u0026gt; Biochemicals and Reagents \u0026gt; Nucleosides, Nucleotides, Oligonucleotides\u003c\/li\u003e\n\u003cli\u003ePack sizes: available in standard TCI research-scale packaging; please confirm the available pack size when ordering\u003c\/li\u003e\n\u003cli\u003eStorage: store according to the manufacturer's stated conditions on the product label\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eStore the product in its original tightly closed container, kept in a cool, dry place and protected from light and moisture, following the storage conditions stated by the manufacturer on the product label. Stock solutions prepared in dimethyl sulfoxide should be kept in sealed, chemically compatible vials and clearly labelled with the preparation date and concentration. Handle the material in a well-ventilated area or a fume hood, wearing gloves, safety glasses, and a laboratory coat, and avoid the generation of dust when weighing. Keep the container away from incompatible materials, use clean and dry spatulas to prevent contamination of the bulk material, and consult the manufacturer's safety data sheet before use and before disposal of any residues.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"100mg","offer_id":48086683156698,"sku":"TCI2510D429224848","price":3233000.0,"currency_code":"IDR","in_stock":true},{"title":"1g","offer_id":48086683189466,"sku":"TCI2510D429224849","price":16836000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D4292.jpg?v=1767107381"},{"product_id":"tci2510d444125034","title":"TCI D4441 520-34-3 Diosmetin","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eDiosmetin is a chemical compound belonging to the phenylpropanoid group and serves as one of the flavonoid derivatives. It plays a crucial role in biochemical and pharmacological research, where its biological activities are extensively studied. These include antioxidant, anti-inflammatory, and neuropharmacological effects, making it a valuable tool in understanding cellular and molecular mechanisms. In the laboratory, Diosmetin is widely used as a starting material for the synthesis of other compounds or as a reagent in assays that evaluate biological activity. Its presence in scientific research is vital for experiments requiring precise and reliable results.\u003c\/p\u003e\n\u003cp\u003eDiosmetin is favored for its stable chemical properties and high purity, which ensure consistent performance in experimental settings. Its molecular structure allows it to interact effectively with various substrates, enhancing its utility in diverse biochemical applications. The compound is colorless and dissolves easily in organic solvents such as ethyl acetate and ethanol. Its chemical stability under normal conditions further supports its use in rigorous scientific investigations. The absence of interfering contaminants ensures that results remain accurate and free from extraneous influences.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, Diosmetin is commonly used in research focused on natural product chemistry, pharmacology, and biochemistry. It is a preferred choice for studies involving plant-derived compounds due to its availability and reliability. Its application in both academic and industrial research settings underscores its importance in advancing scientific knowledge and developing new therapeutic approaches.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBiochemical Research - Diosmetin is ideal for studying antioxidant and anti-inflammatory properties due to its stable chemical structure and high purity.\u003c\/li\u003e\n\u003cli\u003ePharmacological Studies - It is used to evaluate neuropharmacological effects and potential therapeutic applications in drug development.\u003c\/li\u003e\n\u003cli\u003eNatural Product Chemistry - Diosmetin serves as a key reagent in the synthesis of flavonoid derivatives and related compounds.\u003c\/li\u003e\n\u003cli\u003eAnalytical Testing - Its consistent properties make it suitable for use in assays that require precise and reproducible results.\u003c\/li\u003e\n\u003cli\u003eToxicological Investigations - Diosmetin is employed to assess its safety profile and biological interactions in various experimental models.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 520-34-3\u003c\/li\u003e\n\u003cli\u003eCategory: Life Science \u0026gt; Biochemicals and Reagents \u0026gt; Phenylpropanoids, Aromatic Polyketides\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per supplier specifications\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid, colorless powder\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from light and moisture\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eDiosmetin should be stored in a cool, dry environment, away from direct light and moisture to maintain its chemical stability. It is recommended to use airtight containers made of glass or high-density polyethylene to prevent contamination and degradation. In laboratory settings, it is important to handle Diosmetin with appropriate personal protective equipment, such as gloves and safety goggles, to ensure safety during handling. Due to its high purity and stable nature, Diosmetin requires minimal special handling, making it a reliable and safe material for routine use in biochemical and pharmacological experiments. Proper storage and handling procedures help preserve its integrity and ensure accurate experimental outcomes.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48086692102362,"sku":"TCI2510D444125034","price":1827000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D4441.jpg?v=1769141996"},{"product_id":"tci2510d479425499","title":"TCI D4794 4143-62-8 3',4'-Dimethoxyflavone","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI D4794 3',4'-Dimethoxyflavone is a flavone derivative built on the 2-phenyl-4H-chromen-4-one skeleton, carrying two methoxy groups at the 3' and 4' positions of its B ring. In the laboratory it serves a dual role: as a heterocyclic building block for synthesis, and as a reference compound for the methylated flavonoid class. Natural product chemists use it to explore structure–activity relationships within the flavone group, while medicinal chemists employ it as a starting point for further modification toward new and more complex analogues.\u003c\/p\u003e\n\u003cp\u003eThe characteristics that make this compound a preferred choice begin with its rigid, fully conjugated chromone framework, which gives a distinctive ultraviolet absorption profile that is easy to monitor by HPLC with a UV detector or by spectrophotometer. The two methoxy groups on the B ring increase lipophilicity compared with the corresponding hydroxy analogues, so the compound dissolves more readily in organic solvents such as DMSO, methanol, or dichloromethane and shows greater stability toward oxidation. Those same methoxy groups can be demethylated to hydroxy groups whenever a more polar derivative is required.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this material fits naturally into natural product chemistry and medicinal chemistry programmes at universities and research institutes, where flavonoid work is well established. It is typically handled at small synthetic and analytical scale: as a reference standard alongside plant extract profiling, as an intermediate in stepwise derivative synthesis, and as a teaching or method-development material in graduate research groups working on heterocyclic chemistry.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eHeterocyclic synthesis building block — the chromone core provides a stable, reactive scaffold from which more complex flavone analogues can be assembled through stepwise chemical modification.\u003c\/li\u003e\n\u003cli\u003eStructure–activity relationship studies — as a defined methylated flavone, it lets natural product researchers compare substitution patterns systematically across the wider flavone series.\u003c\/li\u003e\n\u003cli\u003eMedicinal chemistry lead modification — its methoxy groups offer clear handles for demethylation or further functionalisation when designing new candidate analogues from a known framework.\u003c\/li\u003e\n\u003cli\u003eHPLC and UV spectrophotometric reference work — the conjugated framework gives a characteristic ultraviolet absorption profile, making the compound straightforward to detect, track, and quantify.\u003c\/li\u003e\n\u003cli\u003ePreparation of more polar derivatives — the 3' and 4' methoxy groups can be converted to hydroxy groups when a research programme requires increased polarity or hydrogen-bonding capability.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI (Tokyo Chemical Industry)\u003c\/li\u003e\n\u003cli\u003eCAS number: 4143-62-8\u003c\/li\u003e\n\u003cli\u003eCatalogue number: D4794\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: available in standard research-scale TCI catalogue pack sizes; please confirm the required size when ordering\u003c\/li\u003e\n\u003cli\u003eStorage: keep in the tightly closed original container, protected from light and moisture, in accordance with the manufacturer's product documentation\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eStore the compound in its original tightly closed container, kept dry and protected from light, and follow the storage conditions stated in the manufacturer's product documentation and safety data sheet. Amber glass vials or the supplied container are suitable; avoid repeated opening that allows moisture ingress. Handle the powder in a fume hood or well-ventilated area using gloves, safety glasses, and a laboratory coat, and avoid generating or inhaling dust. Weigh out only the quantity needed, close the container promptly afterward, and prepare stock solutions in organic solvents such as DMSO or methanol shortly before use. Dispose of residues and contaminated consumables through the institution's chemical waste procedures.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"200mg","offer_id":48086708912346,"sku":"TCI2510D479425499","price":1997000.0,"currency_code":"IDR","in_stock":true},{"title":"1g","offer_id":48086708945114,"sku":"TCI2510D479425500","price":7055000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D4794.jpg?v=1767107990"}],"url":"https:\/\/amiscientific.com\/en\/collections\/tci-l4-antitumor-agents-for-research.oembed?page=3","provider":"AMI Scientific","version":"1.0","type":"link"}