生物活性 | |||
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靶点 |
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描述 | TH588 (2-10μM; 7-10 days) selectively and efficiently eradicates U2OS, HeLa, MDA-MB-231, MCF-7, SW480, and SW620 cells, displaying IC50 values of 1.38, 0.83, 1.03, 1.08, 1.72, 0.8 μM, respectively[1]. | ||
作用机制 | TH588 inhibits MTH1 by forming hydrogen bonds with Phe72 and Met81 and π-π stacking with Phe72. |
实验方案 | |||
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1mg | 5mg | 10mg | |
1 mM 5 mM 10 mM |
3.39mL 0.68mL 0.34mL |
16.94mL 3.39mL 1.69mL |
33.88mL 6.78mL 3.39mL |
参考文献 |
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