2’,3’,5’-Tri-O-acetylinosine

• CAT Number: R000516
• CAS Number: 3181-38-2
• Molecular Formula: C₁₆H₁₈N₄O₈
• Molecular Weight: 394.34
• Purity: ≥95%
• Synonyms: NSC 66386
• Storage: -20°C
• IUPAC Name: [(2R,3R,4R,5R)-3,4-diacetyloxy-5-(6-oxo-1H-purin-9-yl)oxolan-2-yl]methyl acetate
• InChI: InChI=1S/C16H18N4O8/c1-7(21)25-4-10-12(26-8(2)22)13(27-9(3)23)16(28-10)20-6-19-11-14(20)17-5-18-15(11)24/h5-6,10,12-13,16H,4H2,1-3H3,(H,17,18,24)/t10-,12-,13-,16-/m1/s1
• InChIKey: SFEQTFDQPJQUJM-XNIJJKJLSA-N
• SMILES: CC(=O)OC[C@@H]1[C@H]([C@H]([C@@H](O1)N2C=NC3=C2N=CNC3=O)OC(=O)C)OC(=O)C

2’,3’,5’-Tri-O-acetylinosine（Cat No.:R000516）is a chemically modified derivative of inosine, with acetyl groups attached to its hydroxyl moieties to enhance stability and lipophilicity. This compound is widely used in biochemical research and nucleoside analog development. It serves as a precursor in synthetic pathways for antiviral and anticancer agents. The acetyl modifications improve cellular uptake and solubility, making it valuable for studying inosine metabolism and nucleoside transport. Its role in exploring therapeutic nucleosides highlights its importance in drug design and the investigation of nucleoside-based biochemical pathways.