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Apoptosis Pathway

Chemical Structure Cat. No. Product Name CAS No.
BMS202 HCl Chemical Structure
BCP42693 BMS202 HCl BMS202HCl
BMS-202 is a PD-1/PD-L1 interaction inhibitor.
KEA1-97 Chemical Structure
BCP42477 KEA1-97 2138882-71-8
KEA1-97 is a small molecule that disrupts the interaction of thioredoxin with caspase 3.
NY2267 Chemical Structure
BCP41938 NY2267 886053-73-2
NY2267 is a disruptor of Myc-Max interaction, with an IC50 of 36.5 μM.
SRS11-92 Chemical Structure
BCP41935 SRS11-92 1467047-25-1
SRS11-92 is a ferroptosis inhibitor and a derivative of ferrostatin-1.
FR054 Chemical Structure
BCP41907 FR054 10378-06-0
FR054 is an inhibitor of the Hexosamine Biosynthetic Pathway (HBP) enzyme PGM3, with a remarkable anti-breast cancer effect.
BI-3802 Chemical Structure
BCP41514 BI-3802 2166387-65-9 
BI-3802 is a BCL6 inhibitor, with an IC50 of ≤3 nM. BI-3802 shows an IC50 of 43 nM for the cellular BCL6.
Nω-Hydroxy-nor-L-Arginine Dihydrochloride Chemical Structure
BCP41251 Nω-Hydroxy-nor-L-Arginine Dihydrochloride 291758-32-2
nor-NOHA is a potent and reversible inhibitor of rat liver arginase.
UCB-9260 Chemical Structure
BCP40717 UCB-9260 1515888-53-5
UCB-9260 is an orally active inhibitor that inhibits TNF signalling by stabilising an asymmetric form of the trimer.
Mcl1-IN-2 Chemical Structure
BCP40301 Mcl1-IN-2 292057-76-2
Mcl1-IN-2, a hydroxyquinoline derivative, is an Mcl-1 inhibitor.
APG-2575 Chemical Structure
BCP40069 APG-2575 APG2575
APG-2575 is a novel, orally administered small-molecule Bcl-2‒selective inhibitor.
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