生物活性 | |||
---|---|---|---|
描述 | THZ-P1-2 is a pioneering and selective inhibitor of PI5P4K, with an IC50 of 190 nM for PI5P4Kα. It covalently binds to cysteines on a disordered loop in PI5P4Kα/β/γ, leading to autophagy disruption and the upregulation of TFEB signaling. Additionally, THZ-P1-2 exhibits anticancer properties in leukemia cell lines.[1] |
实验方案 | |||
---|---|---|---|
1mg | 5mg | 10mg | |
1 mM 5 mM 10 mM |
1.88mL 0.38mL 0.19mL |
9.41mL 1.88mL 0.94mL |
18.81mL 3.76mL 1.88mL |