| 中文名 | NVP-LCQ195 |
|---|---|
| 英文名 | 4-[(2,6-dichlorobenzoyl)amino]-N-(1-methylsulfonylpiperidin-4-yl)-1H-pyrazole-5-carboxamide |
| 英文别名 |
CS-0840
AT 9311 4-(2,6-dichlorobenzoylamino)-1H-pyrazole-3-carboxylic acid (1-methanesulphonyl-piperidin-4-yl)amide NVP LCQ195 LCQ 195 NVP-LCQ195 |
| 描述 | NVP-LCQ195 (AT9311; LCQ195)是CDK杂环类抑制剂,对CDK1,CDK2,CDK3和CDK5的IC50为1-42 nM。 |
|---|---|
| 相关类别 | |
| 靶点 |
Cdk5/p25:1 nM (IC50) CDK5/p35:1 nM (IC50) Cdk1/cyclin B:2 nM (IC50) cdk2/cyclin A:2 nM (IC50) CDK2/cyclinE:5 nM (IC50) CDK9/cyclinT1:15 nM (IC50) CDK3/Cyclin E:42 nM (IC50) cdk6/cyclin D3:187 nM (IC50) CDK7/Cyclin H/MAT1:3564 nM (IC50) |
| 参考文献 |
| 分子式 | C17H19Cl2N5O4S |
|---|---|
| 分子量 | 460.33500 |
| 精确质量 | 459.05300 |
| PSA | 136.13000 |
| LogP | 3.91620 |
| 储存条件 | -20°C |
|
~93%
902156-99-4 |
| 文献:ASTEX THERAPEUTICS LIMITED Patent: WO2008/1101 A2, 2008 ; Location in patent: Page/Page column 366-367 ; |
|
~%
902156-99-4 |
| 文献:ASTEX THERAPEUTICS LIMITED Patent: WO2008/1101 A2, 2008 ; Location in patent: Page/Page column 369-370 ; |
|
~49%
902156-99-4 |
| 文献:ASTEX THERAPEUTICS LIMITED Patent: WO2007/129066 A1, 2007 ; Location in patent: Page/Page column 97-98 ; |