CAS NO: | 1702809-17-3 |
包装 | 价格(元) |
1mg | 电议 |
5mg | 电议 |
10mg | 电议 |
25mg | 电议 |
50mg | 电议 |
100mg | 电议 |
生物活性 | THZ531 is a selective and covalent inhibitor of bothCDK12andCDK13withIC50s of 158 nM and 69 nM, respectively[1]. | ||||||||||||||||
IC50& Target |
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体外研究 (In Vitro) | The results from Kinase assays demonstrate that THZ531 potently inhibits CDK12 and CDK13 with IC50s of 158 nM and 69 nM, respectively; whereas inhibition of CDK7 and CDK9 is more than 50-fold weaker with IC50s of 8.5 and 10.5 μM, respectively. THZ531 treatment leads to a dramatic and irreversible decrease in Jurkat cell proliferation with an IC50of 50 nM. FACS cell cycle analysis following treatment with escalating doses of THZ531 displays a dose and time-dependent increase in the number of cells exhibiting sub-G1 content. At 50 nM THZ531, no increase in the percentage of apoptotic cells is observed over DMSO control for the time course of the experiment. Higher doses of THZ531 leads to pronounced Annexin V signal with 30 to 40% annexin V-positively stained cells by 72 hrs. A dramatic reduction in elongating Pol II following THZ531 treatment is also observed[1]. | ||||||||||||||||
分子量 | 558.07 | ||||||||||||||||
性状 | Solid | ||||||||||||||||
Formula | C30H32ClN7O2 | ||||||||||||||||
CAS 号 | 1702809-17-3 | ||||||||||||||||
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 : 14.29 mg/mL(25.61 mM;Need ultrasonic) 配制储备液
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以下溶剂前显示的百
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