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Product introduction
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.
Chinese name
PF-477736,Chk1抑制剂, 检查点激酶 1 抑制剂
English name
PF-477736
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
Technical Documents
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PF-477736 10mM in DMSO 1ml

PF-477736 10mM in DMSO 1ml; supplied for laboratory research, analysis, inspection, and scientific procurement use; specifications: 1ml.

item number:P408231-1ml
Product model:1ml
level: 1ml
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