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Chemical Structure Cat. No. Product Name CAS No.
SB 203186 hydrochloride Chemical Structure
BCP42428 SB 203186 hydrochloride 135938-17-9
SB203186 is potent 5-HT4 receptor antagonist with high affinity for human atrial 5-HT4 receptors.
Lenalidomide-4-aminomethyl hydrochloride Chemical Structure
BCP42312 Lenalidomide-4-aminomethyl hydrochloride 444289-05-8
Lenalidomide-4-aminomethyl hydrochloride is the Lenalidomide-based cereblon (CRBN) ligand used in the recruitment of CRBN protein.
Thalidomide-O-C6-NH2 hydrochloride Chemical Structure
BCP42310 Thalidomide-O-C6-NH2 hydrochloride 2245697-88-3
Thalidomide-O-C6-NH2 hydrochloride is a synthesized E3 ligase ligand-linker conjugate used in the PROTAC dTAG-13, a degrader of FKBP12F36V and BET.
NH2-PEG5-C2-NH-Boc Chemical Structure
BCP42279 NH2-PEG5-C2-NH-Boc 189209-27-6
NH2-PEG5-C2-NH-Boc is a PEG-based PROTAC linker can be used in the synthesis of PROTACs.
MUN96006 Chemical Structure
BCP42260 MUN96006 2130996-00-6
MUN96006 is an antagonists of sphingosine-?1-?phosphate (S1P) receptor for prophylaxis and?/or treatment of diseases including fibrotic, inflammatory, autoimmune, metabolic, cardiovascular, and?/or proliferative diseases.
CCW16 Chemical Structure
BCP42239 CCW16 2361138-33-0
CCW16 is targeting ligand for the E3 ubiquitin ligase RNF4 (RING finger protein 4) and can be used in targeted protein degradation (TPD) research or in the synthesis of protein degraders.
Methyl tetrazine OH Chemical Structure
BCP42340 Methyl tetrazine OH 58884-35-8
Methyl tetrazine OH is an alkyl chain-based PROTAC linker that can be used in the synthesis of PROTACs.
Thalidomide-linker 6 Chemical Structure
BCP42249 Thalidomide-linker 6 390367-50-7
Thalidomide-linker 6 is a synthesized E3 ligase ligand-linker conjugate that incorporates the Thalidomide based cereblon ligand and a linker used in PROTAC technology.
Thalidomide-linker 6 hydrochloride Chemical Structure
BCP42246 Thalidomide-linker 6 hydrochloride 2341840-99-9
Thalidomide-linker 6 hydrochloride is a functionalized cereblon ligand for PROTAC that incorporates an E3 ligase ligand plus an alkylC2 linker with terminal amine ready for conjugation to a target protein ligand.
(S,R,S)-AHPC-C9-NH2 hydrochloride Chemical Structure
BCP42237 (S,R,S)-AHPC-C9-NH2 hydrochloride 2376139-50-1
Protein degrader building block (S,R,S)-AHPC-C6-NH2 hydrochloride enables the synthesis of molecules for targeted protein degradation and PROTAC (proteolysis-targeting chimeras) technology.
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