Neu5Troc[1Me,4789Ac]alpha(2-3)Gal[26Bn]-beta-MP TCI M1729

Chemical Identity

CAS No.: 610763-72-9
PubChem: CID 56973700·SID 135727222
Formula: C48H56Cl3NO20
Molecular weight: 1073.3 g/mol
Purity: >98.0%(HPLC)

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: methyl 4-acetyloxy-2-[5-hydroxy-2-(4-methoxyphenoxy)-3-phenylmethoxy-6-(phenylmethoxymethyl)oxan-4-yl]oxy-6-[(1S,2R)-1,2,3-triacetyloxypropyl]-5-(2,2,2-trichloroethoxycarbonylamino)oxane-2-carboxylate
SMILES: CC(=O)OC[C@H]([C@H](C1C(C(CC(O1)(C(=O)OC)OC2C(C(OC(C2OCC3=CC=CC=C3)OC4=CC=C(C=C4)OC)COCC5=CC=CC=C5)O)OC(=O)C)NC(=O)OCC(Cl)(Cl)Cl)OC(=O)C)OC(=O)C
InChIKey: HNINFVMNWIPTPG-IJDKSFGZSA-N

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TCI M1729 610763-72-9 Neu5Troc[1Me,4789Ac]alpha(2-3)Gal[26Bn]-beta-MP is a highly specialized chemical compound used in advanced chemical biology research, particularly in glycoscience. This compound is designed for use in laboratory settings where precise molecular interactions are required, such as in the study of glycan-receptor interactions. Its complex structure enables researchers to explore the molecular mechanisms underlying biological processes, making it a critical tool in modern biochemical investigations.

The compound's unique chemical modifications, including the Troc and Ac groups, make it a preferred choice for synthesizing glycan derivatives with tailored functionalities. These modifications allow for enhanced reactivity and specificity, which are essential in developing compounds for drug discovery and therapeutic applications. The compound’s structural complexity also supports its use in creating synthetic models of natural glycans, aiding in the study of their biological roles.

In Indonesian laboratories, this compound is widely used in applied research areas such as pharmaceutical development, molecular diagnostics, and cellular interaction studies. Its role in creating synthetic glycans with specific biological functions makes it an essential component in both academic and industrial research settings. Researchers in various institutions and universities rely on this compound to advance their understanding of glycoscience and its implications in biomedicine.

TCI brochures (PDF)

Glycosidation 2026-04-14 · p. 10
Reagents for Glyco Chemistry & Biology 5th Edition · p. 86

Related TCI products

Glycan Synthesis Research: This compound is ideal for synthesizing complex glycans that mimic natural structures, aiding in the study of their biological functions and interactions.
Drug Discovery Programs: Its modified structure enables the development of glycan-based therapeutics, supporting the creation of targeted drug candidates for various diseases.
Molecular Diagnostics: The compound’s specificity allows for the design of diagnostic tools that detect glycan-related biomarkers, enhancing the accuracy of disease identification.
Cellular Interaction Studies: Its role in modeling glycan-receptor interactions makes it valuable for investigating how cells communicate and respond to external signals.
Biomedical Research: The compound supports research into glycan-mediated processes, contributing to advancements in understanding disease mechanisms and treatment strategies.

Brand	TCI
CAS number	610763-72-9
Molecular formula	—
Purity	—
Category	Chemistry > Chemical Biology > Glycoscience
Pack sizes	—
Physical form	—
Storage	Store in a cool, dry place away from light

This compound 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 complexity, it is important to handle the compound with appropriate personal protective equipment, such as gloves and safety goggles, to ensure laboratory safety. The compound should be kept in a secure location to prevent accidental exposure. Proper labeling of storage containers is essential for safe handling and to maintain a clear inventory. Regular monitoring of storage conditions is advised to maintain the integrity of the compound and ensure its effectiveness in research applications.

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