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135473-15-3

135473-15-3 Structure

135473-15-3 Structure
IdentificationBack Directory
[Name]

6-Chloropurine -9-beta-D-(3',5'-di-O-benzoyl-2'-deoxy-2'-fluoro)arabinoriboside
[CAS]

135473-15-3
[Synonyms]

9-(3,5-Di-O-benzoyl-2-deoxy-2-fluoro-β-D-arabinofuranosyl)-9H-6-chloropurine
6-Chloropurine-9-β-D-(3’,5’-di-O-benzoyl-2’-deoxy-2’-fluoro)-arabinoriboside
6-Chloro-9-(3,5-di-O-benzoyl-2-deoxy-2-fluoro-?-D-arabinofuranosyl)-9H-purine
9H-Purine, 6-chloro-9-(3,5-di-O-benzoyl-2-deoxy-2-fluoro-β-D-arabinofuranosyl)-
6-Chloropurine -9-beta-D-(3',5'-di-O-benzoyl-2'-deoxy-2'-fluoro)arabinoriboside
6-Chloro-9-(3,5-di-O-benzoyl-2-deoxy-2-fluoro-beta-D-arabinofuranosyl)-9H-purine
((2R,3R,4S,5R)-3-(BENZOYLOXY)-5-(6-CHLORO-9H-PURIN-9-YL)-4-FLUOROTETRAHYDROFURAN-2-YL)METHYL BENZOATE
((2R,3R,4S,5R)-3-(benzoyloxy)-5-(6-chloro-9H-purin-9-yl)-4-fluorotetrahydrofuran-2-yl)methyl benzoate(WXC03256)
[Molecular Formula]

C24H18ClFN4O5
[MDL Number]

MFCD15145215
[MOL File]

135473-15-3.mol
[Molecular Weight]

496.87
Chemical PropertiesBack Directory
[Boiling point ]

665.6±65.0 °C(Predicted)
[density ]

1.51±0.1 g/cm3(Predicted)
[pka]

0.76±0.10(Predicted)
[InChIKey]

MNHSAXRZPYOLSX-OWJXGRTBNA-N
[SMILES]

C(OC)(=O)C1=CC=CC=C1[C@@H]1[C@@H](OC(=O)C2=CC=CC=C2)[C@H](F)[C@H](N2C3=C(N=C2)C(Cl)=NC=N3)O1 |&1:10,11,21,23,r|
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P261-P264-P270-P271-P280-P301+P312-P302+P352-P304+P340-P305+P351+P338-P330-P332+P313-P337+P313-P362-P403+P233-P405-P501
Hazard InformationBack Directory
[Uses]

6-Chloro-9-(3,5-di-O-benzoyl-2-deoxy-2-fluoro-beta-D-arabinofuranosyl)-9H-purine 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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