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Chemical Structure Cat. No. Product Name CAS No.
BD1063 dhydrochloride Chemical Structure
BCP31637 BD1063 dhydrochloride 206996-13-6
BD1063 dhydrochloride is a potent and selective sigma 1 receptor antagonist.
HG-9-91-01 Chemical Structure
BCP25041 HG-9-91-01 1456858-58-4
HG-9-91-01 is a potent and highly selective salt-inducible kinase (SIK) inhibitor with IC50s of 0.92 nM, 6.6 nM and 9.6 nM for SIK1, SIK2 and SIK3 respectively.
EN40 Chemical Structure
BCP31630 EN40 2094547-67-6
EN40 is a potent, selective, and covalent ligand which inhibits aldehyde dehydrogenase 3A1 (ALDH3A1), and impairs lung cancer pathogenicity.
RHC80267 Chemical Structure
BCP31629 RHC80267 83654-05-1
RHC 80267 is a potent and selective inhibitor of diacylglycerol lipase
JWG-071 Chemical Structure
BCP31627 JWG-071 2250323-50-1
JWG-071 is the first reported kinase-selective chemical probe for ERK5.
ZT-12-037-01 Chemical Structure
BCP31626 ZT-12-037-01 2328073-61-4
ZT-12-037-01 is a potent, selective, ATP-competitive STK19 inhibitor. ZT-12-037-01 effectively blocks oncogenic NRAS-driven melanocyte malignant transformation and melanoma growth in vitro and in vivo.
DO-264 Chemical Structure
BCP31625 DO-264 2301866-59-9
DO264 is a novel ABHD12 inhibitor.
GNF4877 Chemical Structure
BCP31624 GNF4877 2041073-22-5
GNF4877 is a potent DYRK1A and GSK3β inhibitor with IC50s of 6 nM and 16 nM.
ANI-7 Chemical Structure
BCP31623 ANI-7 931417-26-4
ANI-7 is a potent and selective (up to 263-fold) inhibitor of breast cancer cells with GI50 of 0.5 uM (MCF-7), via activation the aryl hydrocarbon receptor (AhR) pathway.
Imetit Dihydrobromide Chemical Structure
BCP31622 Imetit Dihydrobromide 32385-58-3
Imetit Dihydrobromide is a histamine H3 receptor (H3R) agonist.
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