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Apoptosis Pathway

Chemical Structure Cat. No. Product Name CAS No.
C25-140 Chemical Structure
BCP30323 C25-140 1358099-18-9
C25-140 is the first in class protein-protein interaction inhibitor of a RING-E3 ligase (TRAF6) / E2 enzyme (Ubc13) binding.
Bax channel blocker Chemical Structure
BCP30816 Bax channel blocker 335165-68-9
Bax channel blocker is a direct allosteric inhibitor of BAX.
BMS-1166 Chemical Structure
BCP30748 BMS-1166 1818314-88-3
BMS-1166 is a potent PD-1/PD-L1 interaction inhibitor with an IC50 of 1.4 nM.
Tetrahydrocurcumin Chemical Structure
BCP18621 Tetrahydrocurcumin 36062-04-1
Tetrahydrocurcumin is isolated and purified from the rhizomes of Curcuma longa L.
GDP366 Chemical Structure
BCP30719 GDP366 501698-03-9
GDP366, a dual inhibitor of survivin and Op18, induces cell growth inhibition, cellular senescence and mitotic catastrophe in human cancer cells.
Epibrassinolide Chemical Structure
BCP20059 Epibrassinolide 78821-43-9
Epibrassinolide is a natural brassinosteroid (BR) derivative, is a plant regulator with a similar structure to mammalian steroids. Epibrassinolide is a potential apoptotic inducer in various cancer cells without affecting the non-tumor cell growth.
UAMC3203 3HCl Chemical Structure
BCP30685 UAMC3203 3HCl UAMC32033HCl
UAMC-3203 is a novel potent, drug-like ferroptosis inhibitor with IC50 of 12 nM, inhibit erastin-induced ferroptotic cell death more potently than Ferrostatin-1; shows an improved protection compared to Fer-1 against multi-organ injury in mice, represents novel lead compounds with therapeutic potential in relevant ferroptosis-driven disease models.
UAMC-3203 Chemical Structure
BCP30684 UAMC-3203 2271358-64-4
UAMC-3203 is a potent and selective Ferroptosis inhibitor with an IC50 of 12 nM.
AC-DEVD-AFC Chemical Structure
BCP18218 AC-DEVD-AFC 201608-14-2
Ac-DEVD-AFC is a fluorogenic substrate (λex=400 nm, λem=530 nm).
GSK547 Chemical Structure
BCP30590 GSK547 2226735-55-1
GSK547 is a highly selective and potent inhibitor of RIP1 kinase that targets RIP1 in vivo.
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