CAS 39007-52-8

Imidazo[1,2-c]pyrimidin-5(6H)-one, 6-β-D-ribofuranosyl-

Description:

Imidazo[1,2-c]pyrimidin-5(6H)-one, 6-β-D-ribofuranosyl- is a nucleoside analog characterized by its unique bicyclic structure, which combines an imidazole and pyrimidine ring. This compound features a ribofuranosyl moiety, which is a sugar component that enhances its biological activity, particularly in the context of nucleic acid metabolism. The presence of the β-D-ribofuranosyl group suggests that it can participate in biochemical processes similar to natural nucleosides, potentially influencing RNA synthesis and function. The compound is of interest in medicinal chemistry and pharmacology due to its potential antiviral and anticancer properties, as it may interfere with viral replication or cellular proliferation. Its CAS number, 39007-52-8, allows for easy identification and retrieval of information regarding its synthesis, properties, and applications in scientific literature. Overall, this compound exemplifies the intersection of organic chemistry and biochemistry, highlighting the importance of structural modifications in developing therapeutic agents.

Formula: C₁₁H₁₃N₃O₅

Synonyms:

• Imidazo[1,2-c]pyrimidin-5(6H)-one, 6-β-D-ribofuranosyl-

N4-Ethenocytidine

CAS: 39007-52-8

N4-Ethenocytidine is a nucleoside analogue that has been synthesized and shown to be an effective inhibitor of the hepatitis C virus. N4-Ethenocytidine prevents the synthesis of viral RNA by attacking the 3'-hydroxyl group of uridine, which is involved in the formation of ribonucleotides. This compound can also inhibit rat liver microsomes through a hydrated attack on carbonyl groups. The reaction products are trifluoroacetic acid and chloride ions. N4-Ethenocytidine's fluorescence properties have been used to identify its reaction intermediates, which include uridylic acid and 4-etheno-N6-isopentenyladenosine.

Formula: C₁₁H₁₃N₃O₅

Purity: Min. 95%

Color and Shape: White Off-White Powder

Molecular weight: 267.24 g/mol

Ref: 3D-NE06244