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Chemical Structure Cat. No. Product Name CAS No.
Cathelicidin LL 37 (human) Chemical Structure
 BCP30243 Cathelicidin LL 37 (human) 154947-66-7
LL-37 is a human cathelicidin that inhibits viral replication and while also playing a role in host defense against infection.
Bobcat339 hydrochloride Chemical Structure
 BCP49654 Bobcat339 hydrochloride 2436747-44-1
Bobcat339 hydrochloride is a potent and selective cytosine-based inhibitor of TET enzyme, with the IC50s of 33 μM and 73 μM for TET1 and TET2, respectively.
β-Cyclodextrin Chemical Structure
 BCP49653 β-Cyclodextrin 7585-39-9
β-Cyclodextrin is a cyclic polysaccharide composed of seven units of glucose (α-D-glucopyranose) linked by α-(1,4) type bonds. β-Cyclodextrin has often been used to enhance the solubility of agents. β-Cyclodextrin has anti-influenza virus H1N1 activities.
α-Cyclodextrine Chemical Structure
 BCP49652 α-Cyclodextrine 10016-20-3
α-Cyclodextrin is a multifunctional, soluble dietary fiber marketed for use as a fiber ingredient.
Boc-NH-PEG(3)-COOH Chemical Structure
 BCP49651 Boc-NH-PEG(3)-COOH 876345-13-0
Boc-NH-PEG(3)-COOH is a cleavable ADC linker used as a linker for antibody-drug conjugates and a PEG-based PROTAC linker that can be used in the synthesis of PROTACs.
Luxdegalutamide Chemical Structure
 BCP49650 Luxdegalutamide 2750830-09-0
Luxdegalutamide is an orally active and potent proteolysis targeting chimera (PROTAC) protein degrader. Luxdegalutamide degrades wild-type androgen receptor (AR) but also relevant AR LBD mutants, including the most prevalent AR L702H, H875Y, and T878A mutations.
BI-2493 Chemical Structure
 BCP49649 BI-2493 2937344-16-4
BI-2493 is a structural analogue of BI-2865 that was optimized for in vivo administration.
RAS-IN-2 Chemical Structure
 BCP49648 RAS-IN-2 2765081-21-6
RAS-IN-2 (RMC-6236) is a potent pan-KRAS inhibitor targeting activation-state KRAS for cancer-related studies.
DATP Chemical Structure
 BCP49642 DATP DATP
BMS-502 Chemical Structure
 BCP49646 BMS-502 2407854-18-4
BMS-502 is a potent dual inhibitor of diacylglycerol kinase (DGK) α and ζ with IC50 of 4.6 nM and 2.1 nM.
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