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2’-Deoxy-2’-fluoro-5-methyl-4’-thio-alpha-D-arabinouridine manufacturers
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| | 2’-Deoxy-2’-fluoro-5-methyl-4’-thio-alpha-D-arabinouridine Basic information |
| Product Name: | 2’-Deoxy-2’-fluoro-5-methyl-4’-thio-alpha-D-arabinouridine | | Synonyms: | 2’-Deoxy-2’-fluoro-5-methyl-4’-thio-alpha-D-arabinouridine;2’-Deoxy-2’-fluoro-5-methyl-4’-thio-β-D-arabinouridine;2'-Deoxy-2'-fluoro-5-methyl-4'-thio-a-D-arabinouridine;2,4(1H,3H)-Pyrimidinedione, 1-(2-deoxy-2-fluoro-4-thio-α-D-arabinofuranosyl)-5-methyl-;2’-Deoxy-2’-fluoro-5-methyl-4’-thio-a-D-arabinouridine | | CAS: | 294868-24-9 | | MF: | C10H13FN2O4S | | MW: | 276.28 | | EINECS: | | | Product Categories: | | | Mol File: | 294868-24-9.mol |  |
| | 2’-Deoxy-2’-fluoro-5-methyl-4’-thio-alpha-D-arabinouridine Chemical Properties |
| density | 1.58±0.1 g/cm3(Predicted) | | pka | 9.55±0.10(Predicted) |
| | 2’-Deoxy-2’-fluoro-5-methyl-4’-thio-alpha-D-arabinouridine Usage And Synthesis |
| Uses | 2’-Deoxy-2’-fluoro-5-methyl-4’-thio-a-D-arabino uridine 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 |
| | 2’-Deoxy-2’-fluoro-5-methyl-4’-thio-alpha-D-arabinouridine Preparation Products And Raw materials |
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