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CAS 161110-00-5

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N4-BENZOYL-3'-DEOXYCYTIDINE

Description:
N4-Benzoyl-3'-deoxycytidine is a modified nucleoside analog that features a benzoyl group at the N4 position of the cytidine base and lacks the hydroxyl group at the 3' position of the ribose sugar, which is characteristic of deoxycytidine. This compound is of interest in the field of medicinal chemistry and molecular biology due to its potential applications in antiviral and anticancer therapies. The modification enhances its stability and may influence its interaction with nucleic acid targets. N4-benzoyl-3'-deoxycytidine can be utilized in various biochemical assays and research studies aimed at understanding nucleoside function and metabolism. Its structural modifications may also affect its binding affinity and selectivity towards specific enzymes or receptors, making it a valuable tool for investigating nucleoside-related processes. As with many nucleoside analogs, the pharmacological properties, including bioavailability and toxicity, are critical factors that determine its therapeutic potential.
Formula:C16H17N3O5
InChI:InChI=1S/C16H17N3O5/c20-9-11-8-12(21)15(24-11)19-7-6-13(18-16(19)23)17-14(22)10-4-2-1-3-5-10/h1-7,11-12,15,20-21H,8-9H2,(H,17,18,22,23)/t11-,12+,15+/m0/s1
InChI key:QUGKQHJTFHHVDD-YWPYICTPSA-N
SMILES:C1[C@H](O[C@H]([C@@H]1O)N2C=CC(=NC2=O)NC(=O)C3=CC=CC=C3)CO
Synonyms:
  • N4-Benzoyl-3'-deoxy-D-cytidine
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