PF-00477736是一个强有力的,有选择性的ATP竞争性的小分子抑制剂,抑制Chk1,此Chk1带有0.49 nM的Ki。该化合物废除DNA损伤诱导的细胞周期阻滞和提高临床重要的化疗药物的细胞毒性,包括吉西他滨和卡铂。 PF-00477736 is a potent, selective ATP-competitive small-molecule inhibitor that inhibits Chk1 with a Ki of 0.49 nM. The compound abrogates cell cycle arrest induced by DNA damage and enhances cytotoxicity of clinically important chemotherapeutic agents, including gemcitabine and carboplatin.
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PF-477736
Dangerous GoodsCAS number:952021-60-2 molecular formula:C22H25N7O2
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Specs
| Chinese alias | - | ||
| English alias | (2R)-2-amino-2-cyclohexyl-N-[2-(1-methyl-1H-pyrazol-4-yl)-9-oxo-3,10,11-triazatricyclo[6.4.1.0,4,13]trideca-1,4(13),5,7,11-pentaen-6-yl]acetamide | SCHEMBL13599879 | DTXSID401025875 | H11453 | NSC800848 | NSC-800848 | PF 00477736 | PF-736,PF-00477736 | DB | ||
| CAS number | 952021-60-2 | molecular formula | C22H25N7O2 |
| molecular weight | 419.48 g/mol | Exact mass | - |
| PSA | 130.000 Ų | logp | 1.5 |
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3
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