Pomalidomide-PEG6-butyl azide
Synonym(s):Crosslinker–E3 Ligase ligand conjugate;Pomalidomide-2-2-2-2-2-2-6-N3, 24-azido-N-(2-(2,6-dioxopiperidin-3-yl)-1,3-dioxoisoindolin-4-yl)-3,6,9,12,15,18-hexaoxatetracosanamide;Protein degrader building block for PROTAC research;Template for synthesis of targeted protein degrader
- Molecular Weight: 0
- Update Date: 2025-01-27 09:38:02
What is Pomalidomide-PEG6-butyl azide?
The Uses of Pomalidomide-PEG6-butyl azide
Protein degrader builiding block Pomalidomide-PEG6-butyl azide enables the synthesis of molecules for targeted protein degradation and PROTAC (proteolysis-targeting chimeras) technology. This conjugate contains a Cereblon (CRBN)-recruiting ligand, a linker with both hydrophobic and hydrophilic moieties, and a pendant azide for click chemistry with 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 azide group, parallel synthesis can be used to more quickly generate PROTAC libraries that feature variation in crosslinker length, composition, and E3 ligase ligand.
Properties of Pomalidomide-PEG6-butyl azide
| storage temp. | 2-8°C |
Safety information for Pomalidomide-PEG6-butyl azide
Computed Descriptors for Pomalidomide-PEG6-butyl azide
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