Combinatorial Multicomponent Access to Natural-Products-Inspired Peptidomimetics: Discovery of Selective Inhibitors of Microbial Metallo-aminopeptidases-Reference-Cited by-同舟云学术

Combinatorial Multicomponent Access to Natural-Products-Inspired Peptidomimetics: Discovery of Selective Inhibitors of Microbial Metallo-aminopeptidases

Published:2014-07-02 Issue:10 Volume:9 Page:2351-2359
ISSN:1860-7179
Container-title:ChemMedChem
language:en
Short-container-title:ChemMedChem

Author:

Méndez Yanira,Pérez-Labrada Karell,González-Bacerio Jorge,Valdés Gilberto,de los Chávez María Á.,Osuna Joel,Charli Jean-Louis,Pascual Isel,Rivera Daniel G.

Publisher

Wiley

Subject

Organic Chemistry,General Pharmacology, Toxicology and Pharmaceutics,Molecular Medicine,Drug Discovery,Biochemistry,Pharmacology

Reference78 articles.

1. Plasmodium falciparum neutral aminopeptidases: new targets for anti-malarials

2. PepN, the Major Suc-LLVY-AMC-hydrolyzing Enzyme inEscherichia coli, Displays Functional Similarity with Downstream Processing Enzymes in Archaea and Eukarya

3. The Role of Tricorn Protease and Its Aminopeptidase-Interacting Factors in Cellular Protein Degradation

4. PepN is the major aminopeptidase in Escherichia coli: insights on substrate specificity and role during sodium-salicylate-induced stress

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