| Identification | Back Directory | [Name]
E3 ligase Ligand-Linker Conjugates 11 | [CAS]
1835705-61-7 | [Synonyms]
(S,R,S)-AHPC-6-5-6-Cl
(S,R,S)-AHPC-(C3-PEG)2-C6-C
VHL Ligand-Linker Conjugates 11
E3 ligase Ligand-Linker Conjugates 11
(S,R,S)-AHPC-C6-PEG1-C3-PEG1-butyl chloride
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)- | [Molecular Formula]
C39H61ClN4O6S | [MDL Number]
MFCD31560481 | [MOL File]
1835705-61-7.mol | [Molecular Weight]
749.443 |
| Hazard Information | Back Directory | [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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Sigma-Aldrich
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