The chemical substance with the name "[(2R,3S,4S,5R)-3,4-diacetoxy-5-(5-amino-4-cyano-imidazol-1-yl)tetrahydrofuran-2-yl]methyl acetate" and CAS number 23192-63-4 is a complex organic compound characterized by its specific stereochemistry and functional groups. It features a tetrahydrofuran ring, which is a five-membered cyclic ether, and is substituted with multiple acetoxy groups, contributing to its reactivity and solubility properties. The presence of an imidazole moiety, which contains nitrogen atoms, suggests potential biological activity, as imidazole derivatives are often found in pharmaceuticals and biologically active compounds. The amino and cyano groups further enhance its chemical reactivity and potential interactions in biological systems. This compound may exhibit properties such as solubility in organic solvents, stability under certain conditions, and the ability to participate in various chemical reactions, making it of interest in medicinal chemistry and synthetic applications. Its specific stereochemistry may also influence its biological activity and interaction with biological targets.

[(2R,3S,4S,5R)-3,4-diacetoxy-5-(5-amino-4-cyano-imidazol-1-yl)tetrahydrofuran-2-yl]methyl acetate

23192-63-4: The chemical substance with the name "[(2R,3S,4S,5R)-3,4-diacetoxy-5-(5-amino-4-cyano-imidazol-1-yl)tetrahydrofuran-2-yl]methyl acetate" and CAS number 23192-63-4 is a complex organic compound characterized by its specific stereochemistry and functional groups. It features a tetrahydrofuran ring, which is a five-membered cyclic ether, and is substituted with multiple acetoxy groups, contributing to its reactivity and solubility properties. The presence of an imidazole moiety, which contains nitrogen atoms, suggests potential biological activity, as imidazole derivatives are often found in pharmaceuticals and biologically active compounds. The amino and cyano groups further enhance its chemical reactivity and potential interactions in biological systems. This compound may exhibit properties such as solubility in organic solvents, stability under certain conditions, and the ability to participate in various chemical reactions, making it of interest in medicinal chemistry and synthetic applications. Its specific stereochemistry may also influence its biological activity and interaction with biological targets.

5-Amino-1-(2'',3'',5''-tri-O-acetyl-b-D-ribofuranosyl)-imidazole-4-carbonitrile

5-Amino-1-(2',3',5'-tri-O-acetyl-b-D-ribofuranosyl)-imidazole-4-carbonitrile is a novel nucleoside analogue that inhibits the viral enzyme ribonucleotide reductase. It has antiviral activity against the herpes viruses, cytomegalovirus, and Epstein Barr virus. 5AADC has also been shown to inhibit DNA synthesis in tumor cells. This compound is currently undergoing clinical trials as an anticancer agent.

CAS 23192-63-4

[(2R,3S,4S,5R)-3,4-diacetoxy-5-(5-amino-4-cyano-imidazol-1-yl)tetrahydrofuran-2-yl]methyl acetate

5-Amino-1-(2'',3'',5''-tri-O-acetyl-b-D-ribofuranosyl)-imidazole-4-carbonitrile

Ref: 7W-GN1147

5-Amino-1-(2',3',5'-tri-O-acetyl-b-D-ribofuranosyl)-imidazole-4-carbonitrile

Ref: 3D-NA11708