| Autor: |
Ceballos, Javier, Grinhagena, Elija, Sangouard, Gontran, Heinis, Christian, Waser, Jerome |
| Předmět: |
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| Popis: |
Easy access to a wide range of structurally diverse stapled peptides is crucial for the development of inhibitors of protein-protein interactions. Herein, we report bis-functional hypervalent iodine reagents for two-component cysteine-cysteine and cysteine-lysine stapling yielding structurally diverse thioalkyne linkers. This stapling method works with unprotected natural amino acid residues and does not require pre-functionalization or metal catalysis. The products are stable to purification and isolation. Post-stapling modification can be accessed via amidation of an activated ester, or via cycloaddition onto the formed thioalkyne group. Increased helicity and binding affinity to MDM2 was obtained for a i,i+7 stapled peptide. |
| Databáze: |
OpenAIRE |
| Externí odkaz: |
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