161599-46-8

5'-Deoxy-2',3'-di-O-acetyl-5-fluorocytidine Chemical Structure
161599-46-8

Chemical Structure

5'-Deoxy-2',3'-di-O-acetyl-5-fluorocytidine

Synonym(s): 2',3'-Di-O-acetyl-5'-deoxy-5-fluorocytidine

  • CAS No.: 161599-46-8
  • Formula:C13H16FN3O6
  • Molecular Weight:329.28

IUPAC Name: (2R,3R,4R,5R)-2-(4-amino-5-fluoro-2-oxopyrimidin-1(2H)-yl)-5-methyltetrahydrofuran-3,4-diyl diacetate

InChIKey: NWJBWNIUGNXJGO-RPULLILYSA-N

SMILES: C[C@@H]1[C@@H](OC(C)=O)[C@@H](OC(C)=O)[C@H](N2C=C(F)C(N)=NC2=O)O1

Biological Activity: 5'-Deoxy-2',3'-di-O-acetyl-5-fluorocytidine (2',3'-Di-O-acetyl-5'-deoxy-5-fluorocytidine) is an antiviral compound that inhibits HBV reverse transcriptase activity. 5'-Deoxy-2',3'-di-O-acetyl-5-fluorocytidine shows potential to control HBV replication in vitro. 5'-Deoxy-2',3'-di-O-acetyl-5-fluorocytidine, as a nucleoside analog, may provide a new option for the suppression of chronic hepatitis B[1].

Cat. No. Product Name Purity Description Pricing
HY-W105601
5'-Deoxy-2',3'-di-O-acetyl-5-fluorocytidine 99.77% 5'-Deoxy-2',3'-di-O-acetyl-5-fluorocytidine (2',3'-Di-O-acetyl-5'-deoxy-5-fluorocytidine) is an antiviral compound that inhibits HBV reverse transcriptase activity. 5'-Deoxy-2',3'-di-O-acetyl-5-fluorocytidine shows potential to control HBV replication in vitro. 5'-Deoxy-2',3'-di-O-acetyl-5-fluorocytidine, as a nucleoside analog, may provide a new option for the suppression of chronic hepatitis B.
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HY-W105601R
5'-Deoxy-2',3'-di-O-acetyl-5-fluorocytidine (Standard) ≥98% 5'-Deoxy-2',3'-di-O-acetyl-5-fluorocytidine (Standard) is the analytical standard of 5'-Deoxy-2',3'-di-O-acetyl-5-fluorocytidine. This product is intended for research and analytical applications. 5'-Deoxy-2',3'-di-O-acetyl-5-fluorocytidine (2',3'-Di-O-acetyl-5'-deoxy-5-fluorocytidine) is an antiviral compound that inhibits HBV reverse transcriptase activity. 5'-Deoxy-2',3'-di-O-acetyl-5-fluorocytidine shows potential to control HBV replication in vitro. 5'-Deoxy-2',3'-di-O-acetyl-5-fluorocytidine, as a nucleoside analog, may provide a new option for the suppression of chronic hepatitis B.
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