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491871-58-0

中文名称 TCS PIM-1 1
英文名称 3-Cyano-4-phenyl-6-(3-bromo-6-hydroxy)phenyl-2(1H)-pyridone
CAS 491871-58-0
分子式 C18H11BrN2O2
分子量 367.2
MOL 文件 491871-58-0.mol
更新日期 2024/04/14 10:33:09
491871-58-0 结构式 491871-58-0 结构式

基本信息

中文别名
PIM-1激酶抑制剂(TCS PIM-1 1)
3-氰基-4-苯基-6-(3-溴-6-羟基苯基)-2(1H)-吡啶酮
6-(5-溴-2-羟基苯)-2-氧代-4-苯基-1,2-二氢吡啶-3-腈
英文别名
CS-1482
TCS PIM-1
SC 204330
TCS PIM-1 1
TCS PIM-1 1, >=98%
TCS PIM-1 1(sc-204330)
SC 204330
TCS PIM 1-1
3-Cyano-4-phenyl-6-(3-bromo-6-hydroxy)phenyl-2(1H)-pyridone
6-(5-Bromo-2-hydroxyphenyl)-1,2-dihydro-2-oxo-4-phenyl-3-pyridinecarbonitrile
3-Pyridinecarbonitrile, 6-(5-bromo-2-hydroxyphenyl)-1,2-dihydro-2-oxo-4-phenyl-
所属类别
生物化工:激动剂抑制剂

物理化学性质

沸点592.6±50.0 °C(Predicted)
密度1.63±0.1 g/cm3(Predicted)
储存条件Store at +4°C
溶解度insoluble in H2O; insoluble in EtOH; ≥12.8 mg/mL in DMSO
酸度系数(pKa)6.93±0.10(Predicted)
形态固体

常见问题列表

生物活性
TCS PIM-1 1 (SC 204330)是一种有效的、选择性的 ATP-competitive Pim-1 kianse 抑制剂,其IC50值为50 nM,对 Pim-2 和 MEK1/MEK2 具有良好的选择性(IC50> 20000 nM)。
靶点
TargetValue
Pim1
(Cell-free assay)
50 nM
体外研究

TCS PIM-1 1 (compound 1), a substituted pyridone scaffold, binds convincingly within the ATP-binding site of Pim-1 suggesting an ATP-competitive inhibitory mechanism. Preliminary data further suggests that TCS PIM-1 1 lacked in vitro inhibitory activity toward related serine/threonine kinases Pim-2 and MEK1/2. Hence, small molecules similar to TCS PIM-1 1 may serve as useful starting scaffolds for the development of other improved yet selective Pim-1 inhibitors. TCS PIM-1 1 serves both as a starting point for SAR chemical syntheses and was used for co-crystallization with Pim-1 protein.

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