Basic information Safety Supplier Related

E3 ligase Ligand-Linker Conjugates 11

Basic information Safety Supplier Related

E3 ligase Ligand-Linker Conjugates 11 Basic information

Product Name:
E3 ligase Ligand-Linker Conjugates 11
Synonyms:
  • E3 ligase Ligand-Linker Conjugates 11
  • (S,R,S)-AHPC-C6-PEG1-C3-PEG1-butyl chloride
  • VHL Ligand-Linker Conjugates 11
  • L-Prolinamide, N-[6-[[5-[(6-chlorohexyl)oxy]pentyl]oxy]-1-oxohexyl]-3-methyl-L-valyl-4-hydroxy-N-[[4-(4-methyl-5-thiazolyl)phenyl]methyl]-, (4R)-
  • (S,R,S)-AHPC-6-5-6-Cl
  • (S,R,S)-AHPC-(C3-PEG)2-C6-C
CAS:
1835705-61-7
MF:
C39H61ClN4O6S
MW:
749.44
Mol File:
1835705-61-7.mol
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E3 ligase Ligand-Linker Conjugates 11 Chemical Properties

Boiling point:
921.3±65.0 °C(Predicted)
Density 
1.152±0.06 g/cm3(Predicted)
storage temp. 
2-8°C
pka
14.08±0.40(Predicted)
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E3 ligase Ligand-Linker Conjugates 11 Usage And Synthesis

Uses

Protein degrader builiding block (S,R,S)-AHPC-C6-PEG1-C3-PEG1-butyl Chloride 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 chloroalkane for reactivity with a nucleophilic group on a 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 chloro group, parallel synthesis can be used to more quickly generate PROTAC libraries that feature variation in crosslinker length, composition, and E3 ligase ligand.

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