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Merck

920762

(S,R,S)-AHPC-benzyl-piperazine hydrochloride

동의어(들):

(2S,4R)-1-((S)-3,3-dimethyl-2-(4-(piperazin-1-ylmethyl)benzamido)butanoyl)-4-hydroxy-N-(4-(4-methylthiazol-5-yl)benzyl)pyrrolidine-2-carboxamide hydrochloride, Crosslinker−E3 Ligase ligand conjugate, Protein degrader building block for PROTAC® research, Template for synthesis of targeted protein degrader, VH032 conjugate

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제품정보 (DICE 배송 시 비용 별도)

실험식(Hill 표기법):
C34H44N6O4S · xHCl
Molecular Weight:
632.82 (free base basis)
UNSPSC Code:
51453014
NACRES:
NA.22
Form:
solid
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도움 문의


ligand

VH032

Quality Level

form

solid

reaction suitability

reactivity: carboxyl reactive, reagent type: ligand-linker conjugate

functional group

amine

storage temp.

2-8°C

SMILES string

CC(N=CS1)=C1C2=CC=C(CNC([C@@H]3C[C@@H](O)CN3C([C@@H](NC(C4=CC=C(CN5CC[ClH](CC5)=N)C=C4)=O)C(C)(C)C)=O)=O)C=C2

Application

Protein degrader building block (S,R,S)-AHPC-benzyl-piperazine hydrochloride enables the synthesis of molecules for targeted protein degradation and PROTAC (proteolysis-targeting chimeras) technology. This conjugate contains a von Hippel-Lindau (VHL)-recruiting ligand, a rigid linker, and a pendant amine for reactivity with a carboxylic acid on the target ligand. Because even slight alterations in ligands and crosslinkers can affect ternary complex formation between the target, E3 ligase, and PROTAC, many analogs are prepared to screen for optimal target degradation. When used with other protein degrader building blocks with a pendant amine, parallel synthesis can be used to more quickly generate PROTAC libraries that feature variation in crosslinker length, composition, and E3 ligase ligand.

Legal Information

PROTAC is a registered trademark of Arvinas Operations, Inc., and is used under license


저장 등급

11 - Combustible Solids

wgk

WGK 3



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시험 성적서(COA)

Lot/Batch Number

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문서 라이브러리 방문


문서

Protein Degrader Building Blocks are a collection of crosslinker-E3 ligand conjugates with a pendant functional group for covalent linkage to a target ligand.


Daniel P Bondeson et al.
Annual review of pharmacology and toxicology, 57, 107-123 (2016-10-13)
Protein homeostasis networks are highly regulated systems responsible for maintaining the health and productivity of cells. Whereas therapeutics have been developed to disrupt protein homeostasis, more recently identified techniques have been used to repurpose homeostatic networks to effect degradation of



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SKUGTIN
920762-50MG04065266056730