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CAS 85079-03-4

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N-Benzoyl-3′-O-methylcytidine

Description:
N-Benzoyl-3′-O-methylcytidine is a modified nucleoside that features a benzoyl group at the nitrogen position of the cytidine base and a methoxy group at the 3′ position of the ribose sugar. This compound is characterized by its structural modifications that enhance its stability and bioactivity compared to unmodified nucleosides. It is typically used in biochemical research and pharmaceutical applications, particularly in the study of nucleic acid interactions and as a potential therapeutic agent. The presence of the benzoyl group can influence the compound's solubility and binding affinity, while the methoxy group may affect its reactivity and interaction with enzymes. N-Benzoyl-3′-O-methylcytidine is also of interest in the synthesis of nucleoside analogs and can serve as a building block in the development of antiviral and anticancer drugs. Its unique structural features make it a valuable compound in the field of medicinal chemistry and molecular biology.
Formula:C17H19N3O6
InChI:InChI=1S/C17H19N3O6/c1-25-14-11(9-21)26-16(13(14)22)20-8-7-12(19-17(20)24)18-15(23)10-5-3-2-4-6-10/h2-8,11,13-14,16,21-22H,9H2,1H3,(H,18,19,23,24)/t11-,13-,14-,16-/m1/s1
InChI key:InChIKey=HBJGWSUTFFOKLJ-XKVFNRALSA-N
SMILES:O[C@H]1[C@@H](O[C@H](CO)[C@H]1OC)N2C(=O)N=C(NC(=O)C3=CC=CC=C3)C=C2
Synonyms:
  • N-Benzoyl-3′-O-methylcytidine
  • Cytidine, N-benzoyl-3′-O-methyl-
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