Discovery of Fluoromethylketone-Based Peptidomimetics as Covalent ATG4B (Autophagin-1) Inhibitors
摘要:
ATG4B or autophagin-1 is a cysteine protease that cleaves ATG8 family proteins. ATG4B plays essential roles in the autophagosome formation and the autophagy pathway. Herein we disclose the design and structural modifications of a series of fluoromethylketone (FMK)-based peptidomimetics as highly potent ATG4B inhibitors. Their structure activity relationship (SAR) and protease selectivity are also discussed.
Recherches sur la formation et la transformation de dérivés organiques du fluor II. Sur la synthèse et l'estérification d'amino-alcools fluorés
作者:Emile Cherbuliez、A. Yazgi、J. Rabinowitz
DOI:10.1002/hlca.19600430425
日期:——
The syntheses of monofluorinated amino-alcohols (with primary, secondary and tertiary amino groups and also with quaternary ammonium groups) and of their phosphoric and acetic esters are described.
描述了单氟化氨基醇(具有伯,仲和叔氨基以及还具有季铵基)及其磷酸酯和酸性酯的合成。
Discovery of Fluoromethylketone-Based Peptidomimetics as Covalent ATG4B (Autophagin-1) Inhibitors
ATG4B or autophagin-1 is a cysteine protease that cleaves ATG8 family proteins. ATG4B plays essential roles in the autophagosome formation and the autophagy pathway. Herein we disclose the design and structural modifications of a series of fluoromethylketone (FMK)-based peptidomimetics as highly potent ATG4B inhibitors. Their structure activity relationship (SAR) and protease selectivity are also discussed.