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Chemical Structure Cat. No. Product Name CAS No.
MTX115325 Chemical Structure
 BCP49673 MTX115325 2750895-97-5
MTX115325 is an orally active, brain-penetrating USP30 inhibitor (IC50=12 nM) with neuroprotective activity.
ARV393 Chemical Structure
 BCP49670 ARV393 2851885-95-3
ARV-393 is an orally active PROTAC degrader targeting BCL6. ARV-393 utilizes the ubiquitin-proteasome system to target the degradation of BCL6. ARV-393 has DC50 and GI50 values of <1 nM in multiple cell lines of diffuse large B-cell lymphoma (DLBCL) and Burkitt lymphoma (BL). ARV-393 also demonstrated considerable tumor suppressor activity in tumor xenograft models.
Hematin porcine Chemical Structure
 BCP49671 Hematin porcine 15489-90-4
Hematin is an iron-containing porphyrin. It is used for testing in vitro activities of the Rx-01 oxazolidinones against hospital and community pathogens.
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.
DATP Chemical Structure
 BCP49642 DATP DATP
TL 12-186 Chemical Structure
 BCP49644 TL 12-186 2250025-88-6
TL12-186 is a Cereblon-dependent kinase degrader that degrades CDK, BTK, FLT3, Aurora and other kinases.TL12-186 inhibits CDK2/cyclin A and CDK9/cyclin T1 with IC50s of 73 and 55 nM, respectively.
H-Gly-hyp-ala-OH Chemical Structure
 BCP49639 H-Gly-hyp-ala-OH 62147-09-5
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