CAS NO: | 94164-88-2 |
包装 | 价格(元) |
10 mM * 1 mL in DMSO | 电议 |
5mg | 电议 |
10mg | 电议 |
50mg | 电议 |
100mg | 电议 |
200mg | 电议 |
500mg | 电议 |
1 g | 电议 |
生物活性 | PKM2-IN-1 is apyruvate kinaseM2(PKM2) inhibitor with anIC50of 2.95 μM. | ||||||||||||||||
IC50& Target | IC50: 2.95 μM (PKM2)[1] | ||||||||||||||||
体外研究 (In Vitro) | PKM2-IN-1 is a pyruvate kinase M2 (PKM2) inhibitor with an IC50of 2.95±0.53 μM. Results show that most of the tested compounds exhibit some degree of PKM2 inhibition and some compounds, such as PKM2-IN-1 (compound 3k) and 6d, display more potent activity than the positive control shikonin. The representative compounds PKM2-IN-1, 6d display dose-dependent inhibition of PKM2 with less inhibition of PKM1 and PKL like shikonin. Among all tested compounds, the most potent compounds are 3a, PKM2-IN-1 and 3r, which exhibit IC50values against HCT116 and Hela cells ranging from 0.39 to 0.41 μM, 0.18 to 0.29 μM and 0.18 to 0.38 μM, respectively[1]. | ||||||||||||||||
分子量 | 345.48 | ||||||||||||||||
性状 | Solid | ||||||||||||||||
Formula | C18H19NO2S2 | ||||||||||||||||
CAS 号 | 94164-88-2 | ||||||||||||||||
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 : 10 mg/mL(28.95 mM;ultrasonic and warming and heat to 60℃) 配制储备液
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