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CAS 13484-66-7

:

[(2R,3R,4R,5R)-5-[6-(benzylamino)purin-9-yl]-3,4-dihydroxy-oxolan-2-yl ]methoxyphosphonic acid

Description:
The chemical substance with the name "[(2R,3R,4R,5R)-5-[6-(benzylamino)purin-9-yl]-3,4-dihydroxy-oxolan-2-yl]methoxyphosphonic acid" and CAS number 13484-66-7 is a nucleotide analog that exhibits significant biological activity, particularly in the context of antiviral and anticancer research. This compound features a purine base, which is a key structural component that allows it to interact with nucleic acid synthesis pathways. The presence of multiple hydroxyl groups contributes to its solubility and potential reactivity, while the methoxyphosphonic acid moiety enhances its ability to mimic natural nucleotides. Its stereochemistry, indicated by the (2R,3R,4R,5R) configuration, is crucial for its biological function, as it influences how the molecule interacts with enzymes and cellular targets. Overall, this compound is of interest in medicinal chemistry for its potential therapeutic applications, particularly in inhibiting viral replication and modulating cellular processes.
Formula:C17H18N5O7P
InChI:InChI=1/C17H20N5O7P/c23-13-11(7-28-30(25,26)27)29-17(14(13)24)22-9-21-12-15(19-8-20-16(12)22)18-6-10-4-2-1-3-5-10/h1-5,8-9,11,13-14,17,23-24H,6-7H2,(H,18,19,20)(H2,25,26,27)/p-2/t11-,13-,14-,17-/m1/s1
Synonyms:
  • Benzyl-amp
  • Benzyl-adenosine monophosphate
  • N6-Benzyladenosine-5'-phosphate
  • Nsc 255523
  • N(6)-Benzyladenosine-5'-monophosphate
  • N-benzyladenosine 5'-(dihydrogen phosphate)
  • N-benzyl-9-(5-O-phosphonopentofuranosyl)-9H-purin-6-amine
  • N-benzyl-5'-O-phosphonatoadenosine
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