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Chemical Structure Cat. No. Product Name CAS No.
D-erythro-Sphingosine HCl Chemical Structure
BCP40404 D-erythro-Sphingosine HCl 2637-72-5
D-erythro-Sphingosine is an inhibitor of protein kinase C and calmodulin-dependent enzymes, but may stimulate mast cells by activation of protein kinase C.
PF-06679142 Chemical Structure
BCP40393 PF-06679142 1467059-66-0
PF-06679142 is a potent AMPK activator.
SRX3207 Chemical Structure
BCP40266 SRX3207 2254693-15-5
SRX3207 is an orally active dual inhibitor of Syk-PI3K with IC50 of 39.9 nM, 31200 nM, 3070 nM, 3070 nM, 244 nM, 388 nM, 9790 nM for Syk, Zap70, BRD41, BRD42, PI3K alpha, PI3K delta, PI3K gamma, respectively.
DDP-38003 2HCl Chemical Structure
BCP39854 DDP-38003 2HCl 1831167-98-6
DDP-38003 2HCl is an orally available inhibitor of histone lysine-specific demethylase 1A (LSD1).
LLY-283 Chemical Structure
BCP39701 LLY-283 2040291-27-6
LLY-283 is an inhibitor of protein arginine methyltransferase 5 (PRMT5) with antitumor activity. It potently suppresses cancer growth via inhibiting PRMT5 expressed in breast cancer, gastric cancer, glioblastoma, and lymphoma cells.
Resminostat hydrochloride Chemical Structure
BCP39644 Resminostat hydrochloride 1187075-34-8
Resminostat HCl is a potent inhibitor of HDAC1/3/6.
Tazemetostat hydrobromide Chemical Structure
BCP39175 Tazemetostat hydrobromide 1467052-75-0
Tazemetostat is a potent, selective, and orally bioavailable small-molecule inhibitor of EZH2 enzymatic activity.
VZ185 Chemical Structure
BCP38781 VZ185 2306193-61-1
VZ185 is an effective and selective dual BRD7/9 PROTAC degrader (DC50s: 4.5 and 1.8 nM, respectively).
BIX 01294 trihydrochloride hydrate Chemical Structure
BCP38667 BIX 01294 trihydrochloride hydrate 1808255-64-2
BIX 01294 trihydrochloride hydrate, a diazepin-quinazolinamine derivative, is a histone-lysine methyltransferase (HMTase) inhibitor that modulates the epigenetic status of chromatin.
Fuzuopali Chemical Structure
BCP38585 Fuzuopali 1358715-18-0
Fluzoparib is a selective poly [ADP-ribose] polymerase 1 (PARP1) and poly [ADP-ribose] polymerase 2 inhibitor (PARP2).
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