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Chemical Structure Cat. No. Product Name CAS No.
BCI-121 Chemical Structure
 BCP30688 BCI-121 432529-82-3
BCI-121 is an SMYD3 inhibitor. It acts by impairing cancer cell growth.
Remetinostat Chemical Structure
 BCP30561 Remetinostat 946150-57-8
Remetinostat (SHP-141) is a hydroxamic acid-based inhibitor of histone deacetylase enzymes (HDAC) which is under development for the treatment of cutaneous T-cell lymphoma.
E-7386 Chemical Structure
 BCP30544 E-7386 1799824-08-0
E-7386 is an orally active CBP/beta-catenin modulator.
T-3775440 Chemical Structure
 BCP30535 T-3775440 1422620-34-5
T-3775440 is a novel potent, selecitve, irreversible LSD1 inhibitor with IC50 of 2.1 nM.
T-3775440 hydrochloride Chemical Structure
 BCP30534 T-3775440 hydrochloride 1422535-52-1
T-3775440 hydrochloride is a potent, selecitve, irreversible LSD1 inhibitor.
Corin Chemical Structure
 BCP30529 Corin 1808113-09-8
Corin is a dual inhibitor of histone lysine specific demethylase (LSD1) and histone deacetylase (HDAC), with a Ki(inact) of 110 nM for LSD1 and an IC50 of 147 nM for HDAC1.
INCB054329 Racemate Chemical Structure
 BCP30528 INCB054329 Racemate 1628607-62-4
INCB054329 Racemate is a BET protein inhibitor.
(S)-JQ-35 Chemical Structure
 BCP30522 (S)-JQ-35 1349719-98-7
(S)-JQ-35 is an inhibitor of the Bromodomain and Extra-Terminal (BET) family bromodomain-containing proteins with potential antineoplastic activity.
PROTAC BRD9 Degrader-1 Chemical Structure
 BCP30517 PROTAC BRD9 Degrader-1 2097971-01-0
PROTAC BRD9 Degrader-1 is a lead PROTAC BRD9 chemical degrader (IC50=13.5 nM), which can be used as a selective probe useful for the study of BAF complex biology.
PROTAC BET Degrader-1 Chemical Structure
 BCP30516 PROTAC BET Degrader-1 2093386-22-0
PROTAC BET Degrader-1 is a potent BET degrader based on PROTAC, decreasing BRD2, BRD3, and BRD4 protein levels at low concentration.
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