KPT-185 is an orally bioavailable selective inhibitor of CRM1 amd displayes potent antiproliferative properties at submicromolar concentrations (IC50 values:100-500nM), induced apoptosis (average 5-fold increase), cell-cycle arrest, and myeloid differentiation in AML cell lines and patient blasts.
MoreASP3026是高活性ALK抑制剂,IC50为3.5 nM。
MoreAT101乙酸盐对Bcl-2, Bcl-xL和Mcl-1的结合Ki值分别为0.32,0.48和0.18uM。
MoreIloperidone是D2/5-HT2受体拮抗剂,可作用于精神分裂症。
MoreINO-1001是PARP抑制剂,IC50为3 nM。
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