中文名 | AZ6102 |
英文名 | AZ6102 |
别名 | 化合物AZ6102 REL-2-[4-[6-[(3R,5S)-3,5-二甲基-1-哌嗪基]-4-甲基-3-吡啶基]苯基]-3,7-二氢-7-甲基-4H-吡咯并[2,3-D]嘧啶-4-酮 |
英文别名 | AZ6102 CS-2332 AZ 6102 AZ-6102 2-(4-(6-((3S,5R)-3,5-Dimethylpiperazin-1-yl)-4-methylpyridin-3-yl)phenyl)-7-methyl-3Hpyrrolo[2,3-d]pyrimidin-4(7H)-one rel-2-[4-[6-[(3R,5S)-3,5-Dimethyl-1-piperazinyl]-4-methyl-3-pyridinyl]phenyl]-3,7-dihydro-7-methyl-4H-pyrrolo[2,3-d]pyrimidin-4-one 4H-Pyrrolo[2,3-d]pyrimidin-4-one, 2-[4-[6-[(3R,5S)-3,5-dimethyl-1-piperazinyl]-4-methyl-3-pyridinyl]phenyl]-3,7-dihydro-7-methyl-, rel- |
CAS | 1645286-75-4 |
化学式 | C25H28N6O |
分子量 | 428.53 |
密度 | 1.31±0.1 g/cm3(Predicted) |
沸点 | 657.6±65.0 °C(Predicted) |
溶解度 | 10毫米DMSO |
酸度系数 | 8.70±0.60(Predicted) |
存储条件 | -20℃ |
体外研究 | AZ6102 is a potent dual TNKS1 and TNKS2 inhibitor, with IC 50 s of 3 nM and 1 nM, respectively. AZ6102 alao has 100-fold selectivity against other PARP family enzymes, with IC 50 s of 2.0 μM, 0.5 μM, and >3 μM, for PARP1, PARP2, and PARP6, respectively. AZ6102 shows Wnt pathway inhibition in DLD-1 cells. |
1mg | 5mg | 10mg | |
---|---|---|---|
1 mM | 2.334 ml | 11.668 ml | 23.336 ml |
5 mM | 0.467 ml | 2.334 ml | 4.667 ml |
10 mM | 0.233 ml | 1.167 ml | 2.334 ml |
5 mM | 0.047 ml | 0.233 ml | 0.467 ml |
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