Glycyrrhizin TCI G0150

Chemical Identity

Other names: Glycyrrhizic Acid
CAS No.: 1405-86-3
PubChem: CID 14982·SID 87570348
Formula: C42H62O16
Molecular weight: 822.94 g/mol
Purity: >75.0%(HPLC)
Reference databases: ChEBI·ChemSpider·ECHA·Wikipedia

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: (2S,3S,4S,5R,6R)-6-[(2S,3R,4S,5S,6S)-2-[[(3S,4aR,6aR,6bS,8aS,11S,12aR,14aR,14bS)-11-carboxy-4,4,6a,6b,8a,11,14b-heptamethyl-14-oxo-2,3,4a,5,6,7,8,9,10,12,12a,14a-dodecahydro-1H-picen-3-yl]oxy]-6-carboxy-4,5-dihydroxyoxan-3-yl]oxy-3,4,5-trihydroxyoxane-2-c
SMILES: CC1(C2CCC3(C(C2(CCC1OC4C(C(C(C(O4)C(=O)O)O)O)OC5C(C(C(C(O5)C(=O)O)O)O)O)C)C(=O)C=C6C3(CCC7(C6CC(CC7)(C)C(=O)O)C)C)C)C
InChIKey: LPLVUJXQOOQHMX-QWBHMCJMSA-N
MDL: MDL00065194

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Glycyrrhizin TCI G0150, with CAS number 1405-86-3, is a chemical compound widely used in laboratory research across chemistry and biological sciences. Derived from the root of the licorice plant *Glycyrrhiza glabra*, this compound is valued for its diverse pharmacological properties. It plays a crucial role in various studies, including anti-inflammatory, antiviral, and antitumor research. Its presence in laboratories supports the development of new drugs and the analysis of active compounds, making it an essential tool for scientific investigation.

One of the key reasons Glycyrrhizin is preferred in laboratories is its molecular structure, which consists of a complex glycoside. This structure contributes to its solubility and stability, allowing it to interact effectively with proteins and enzymes. These interactions make it highly suitable for molecular interaction studies. Additionally, its high purity and consistent quality ensure reliable results in experiments, making it a trusted choice for researchers seeking reproducible outcomes.

In Indonesian laboratories, Glycyrrhizin is commonly used in applied research projects. It is integral to the development of modern traditional medicines, the analysis of active compounds from plants, and pharmacological studies. Its versatility and reliability have made it a staple in both academic and industrial research settings, supporting a wide range of scientific inquiries.

TCI brochures (PDF)

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Obesity_Diabete Research Reagents 2026-07-10 · p. 1
Traditional Medicine/Crude Medicine Research Reagents 2024-09-11 · p. 1
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Anti-inflammatory research benefits from Glycyrrhizin’s ability to modulate inflammatory pathways, making it ideal for studying its therapeutic effects.
Antiviral studies utilize Glycyrrhizin due to its potential to inhibit viral replication, supporting research into viral infection mechanisms.
Antitumor investigations rely on Glycyrrhizin’s capacity to interfere with cancer cell growth, aiding in the development of novel therapeutic strategies.
Molecular interaction studies benefit from its ability to bind with proteins and enzymes, providing insights into biochemical processes.
Drug development projects use Glycyrrhizin as a starting material for synthesizing new compounds, supporting pharmaceutical innovation.

Brand	TCI
CAS number	1405-86-3
Molecular formula	—
Purity	—
Category	Chemistry > Chemical Biology > Glycoscience
Pack sizes	Available in various quantities as per standard laboratory requirements
Physical form	Solid powder
Storage	Store in a cool, dry place away from light and moisture

Glycyrrhizin should be stored in a cool, dry environment, away from direct light and moisture to maintain its stability and purity. It is recommended to use airtight containers to prevent contamination and degradation. Due to its chemical nature, 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 traceability and safe handling. Regular monitoring of storage conditions ensures the compound remains suitable for use in research applications. Always follow standard laboratory safety protocols when working with this compound to minimize risks and ensure optimal performance in experiments.

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