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ChemicalBook--->CAS DataBase List--->205171-04-6

205171-04-6

205171-04-6 Structure

205171-04-6 Structure
IdentificationBack Directory
[Name]

6-Chloro-9-(2,3,5-tri-O-benzoyl-2-C-methyl-beta-D-ribofuranosyl)-9H-purine
[CAS]

205171-04-6
[Synonyms]

6-Chloro-9-(2,3,5-tri-O-benzoyl-2-C-Methyl-β-D-ribofuranosyl)-9H-purine
6-Chloro-9-(2,3,5-tri-O-benzoyl-2-C-methyl-β-D-ribofuranosyl)-9H-purine
6-Chloro-9-(2,3,5-tri-O-benzoyl-2-b-C-methyl-β-D-ribofuranosyl)-9H-purine
9H-Purine, 6-chloro-9-(2,3,5-tri-O-benzoyl-2-C-methyl-β-D-ribofuranosyl)-
6-CHLORO-9-(2,3,5-TRI-O-BENZOYL-2-C-METHYL-BETA-D-RIBOFURANOSYL)-9H-PURINE
(2R,3R,4R,5R)-5-((benzoyloxy)methyl)-2-(6-chloro-9H-purin-9-yl)-3-methyltetrahydrofuran-3,4-diyl dibenzoate
[Molecular Formula]

C32H25ClN4O7
[MDL Number]

MFCD28957715
[MOL File]

205171-04-6.mol
[Molecular Weight]

613.02
Chemical PropertiesBack Directory
[Boiling point ]

757.0±70.0 °C(Predicted)
[density ]

1.41
[pka]

0.76±0.10(Predicted)
Hazard InformationBack Directory
[Uses]

6-Chloro-9-(2,3,5-tri-O-benzoyl-2-C-methyl-beta-D-ribofuranosyl)-9H-purine dibenzoate is a purine nucleoside analog. Purine nucleoside analogs have broad antitumor activity targeting indolent lymphoid malignancies. Anticancer mechanisms in this process rely on inhibition of DNA synthesis, induction of apoptosis, etc[1].
[References]

[1] Robak T, Robak P. Purine nucleoside analogs in the treatment of rarer chronic lymphoid leukemias. Curr Pharm Des. 2012;18(23):3373-88. DOI:10.2174/138161212801227005
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