(S,R,S)-AHPC-PEG2-butyl alkyne

Synonyms (s): (2S,4R)-1-((S)-3,3-Dimethyl-2-(2-(2-(oct-7-yn-1-yloxy)ethoxy)acetamido)butanoyl)-4-hydroxy-N-(4-(4-methylthiazol-5-yl)benzyl)pyrrolidine-2-carboxamide, (S,R,S)-AHPC-2-2-6-alkyne, Crosslinker–E3 Ligase ligand conjugate, Protein degrader building block for PROTAC® research, Template for synthesis of targeted protein degrader, VH032 conjugate

Empirical Formula (Hill Notation): C₃₄H₄₈N₄O₆S

Size: 50 mg

Product Introduction

Molecular Weight	640.83
Assay	≥95%
Form	(Liquid or Semi-solid or Paste or Solid)
Reaction Suitability	Reaction type: click chemistry
Smiles String	O=C(N[C@H](C(N1[C@H](C(NCC2=CC=C(C3=C(C)N=CS3)C=C2)=O)C[C@@H](O)C1)=O)C(C)(C)C)COCCOCCCCCCC#C
Storage Temp.	2-8 °C

Application

Protein degrader builiding block (S,R,S)-AHPC-PEG2-butyl alkyne 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 linker with both hydrophobic and hydrophilic moieties, and a pendant alkyne for click chemistry with an azide 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 alkyne group, parallel synthesis can be used to more quickly generate PROTAC libraries that feature variation in crosslinker length, composition, and E3 ligase ligand.

Safety Information

Storage Class Code	12 - Non Combustible Liquids
WGK	WGK 3

For research use only. Not for clinical use.