CAS NO: | 942947-93-5 |
包装 | 价格(元) |
5mg | 电议 |
10mg | 电议 |
50mg | 电议 |
100mg | 电议 |
200mg | 电议 |
500mg | 电议 |
生物活性 | CCT129202 is anaurorakinase inhibitor withIC50s of 42, 198, and 227 nM foraurora A, B and C, respectively. | ||||||||||||||||
IC50& Target[1] |
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体外研究 (In Vitro) | CCT129202 causes the accumulation of human tumor cells with z4N DNA content, leading to apoptosis. CCT129202 is found to induce apoptosis with GI50values that ranges between 0.08 and 1.7 μM. CCT120202-treated human tumor cells shows a delay in mitosis, abrogation of nocodazole-induced mitotic arrest, and spindle defects. CCT129202 Causes p21Up-regulation, Rb Hypophosphorylation, and H2F-DependentTK1Down-regulation[1]. | ||||||||||||||||
体内研究 (In Vivo) | Growth of HCT116 xenografts in nude mice is inhibited after i.p. administration of CCT129202. p21, the cyclin-dependent kinase inhibitor, is induced by CCT129202. Up-regulation of p21 by CCT129202 in HCT116 cells led to Rb hypophosphorylation and E2F inhibition, contributing to a decrease in thymidine kinase 1 transcription[1]. | ||||||||||||||||
分子量 | 497.02 | ||||||||||||||||
性状 | Solid | ||||||||||||||||
Formula | C23H25ClN8OS | ||||||||||||||||
CAS 号 | 942947-93-5 | ||||||||||||||||
运输条件 | Room temperature in continental US; may vary elsewhere. | ||||||||||||||||
储存方式 |
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溶解性数据 | In Vitro: DMSO : 1 mg/mL(2.01 mM;Need ultrasonic) 配制储备液
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