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Chemical Structure Cat. No. Product Name CAS No.
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).
GSK3368715 dihydrochloride Chemical Structure
 BCP38359 GSK3368715 dihydrochloride 1628925-77-8
GSK3368715 dihydrochloride is a novel potent type-I protein arginine methyltransferases (PRMTs) inhibitor.
Phorbol 12,13-dibutyrate Chemical Structure
 BCP38374 Phorbol 12,13-dibutyrate 37558-16-0
Phorbol 12,13-dibutyrate is a PKC activator and a potent skin tumor promoter.
TFLLR-NH2 Chemical Structure
 BCP38224 TFLLR-NH2 197794-83-5
TFLLR-NH2, derived from the protease-activated receptor-1 (PAR1), is a selective PAR1 agonist with an EC50 of 1.9 μM.
VTP50469 fumarate Chemical Structure
 BCP38003 VTP50469 fumarate 2169919-29-1
VTP50469 fumarate is a highly selective and orally active inhibitor of Menin-MLL interaction (Ki: 104 pM), and has potently anti-leukemia activity.
MT 63-78 Chemical Structure
 BCP38015 MT 63-78 1179347-65-9
MT 63-78 is a direct activator of AMPK, and an inhibitor of prostate cancer growth by blocking lipogenesis.
LEM-14 Chemical Structure
 BCP38013 LEM-14 1814881-70-3
LEM-14 is a specific NSD2 inhibitor.
TM2-115 Chemical Structure
 BCP38007 TM2-115 1197196-47-6
TM2-115 is a potent histone methyltransferase inhibitor with rapid antimalarial activity against all blood stage forms in Plasmodium falciparum
LP99 Chemical Structure
 BCP38006 LP99 1808951-93-0
LP99 is the First Selective BRD7/9 Bromodomain Inhibitor.
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