Z-VAD(OH)-FMK (Caspase Inhibitor VI) 1mg | Purity Not Available
Selleck Chemicals
Z-VAD(OH)-FMK (Caspase Inhibitor VI) is an irreversible pan-caspase inhibitor.
More Information Supplier PageZ-VAD(OH)-FMK (Caspase Inhibitor VI) is an irreversible pan-caspase inhibitor.
More Information Supplier PageZ-VAD(OH)-FMK (Caspase Inhibitor VI) is an irreversible pan-caspase inhibitor.
More Information Supplier PageGlyH-101 is a selective and reversible CFTR inhibitor with Ki of 4.3 μM.
More Information Supplier PageGlyH-101 is a selective and reversible CFTR inhibitor with Ki of 4.3 μM.
More Information Supplier PageGANT61 (NSC 136476) is an inhibitor for GLI1 as well as GLI2-induced transcription, inhibits hedgehog with IC50 of 5 μM in GLI1 expressing HEK293T cell, displays selectivity over other pathways, such as TNF and glucocorticoid receptor gene transactivation. GANT61 induces apoptosis and activates protective autophagy in LX-2 cells.
More Information Supplier PageASP3026 is a novel and selective inhibitor for ALK with IC50 of 3.5 nM. Phase 1.
More Information Supplier PageLomeguatrib (PaTrin-2) is a potent inhibitor of O6-alkylguanine-DNA-alkyltransferase with IC50 of 5 nM.
More Information Supplier PageMidostaurin is a multi-targeted kinase inhibitor, including PKCα/β/γ, Syk, Flk-1, Akt, PKA, c-Kit, c-Fgr, c-Src, FLT3, PDFRβ and VEGFR1/2 with IC50 ranging from 80-500 nM.
More Information Supplier PageVorapaxar (SCH 530348, MK-5348) is a potent and orally active thrombin receptor (PAR-1) antagonist with Ki of 8.1 nM.
More Information Supplier PageVorapaxar (SCH 530348, MK-5348) is a potent and orally active thrombin receptor (PAR-1) antagonist with Ki of 8.1 nM.
More Information Supplier Page