Synthesis and evaluation of new tyrosyl-tRNA synthetase inhibitors as antibacterial agents based on a N2-(arylacetyl)glycinanilide scaffold-Reference-Cited by-同舟云学术

Synthesis and evaluation of new tyrosyl-tRNA synthetase inhibitors as antibacterial agents based on a N2-(arylacetyl)glycinanilide scaffold

Published:2015-09 Issue: Volume:102 Page:631-638
ISSN:0223-5234
Container-title:European Journal of Medicinal Chemistry
language:en
Short-container-title:European Journal of Medicinal Chemistry

Author:

Xiao Zhu-Ping,Wei Wei,Wang Peng-Fei,Shi Wei-Kang,Zhu Na,Xie Me-Qun,Sun Yu-Wen,Li Ling-Xia,Xie Yong-Xiang,Zhu Liang-Song,Tang Nian,Ouyang Hui,Li Xian-Hui,Wang Guang-Cheng,Zhu Hai-Liang

Funder

National Natural Science Foundation of China

Hunan Provincial Natural Science Foundation of China

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Pharmacology,General Medicine

Reference25 articles.

1. Mechanism and evolution of multidomain aminoacyl-tRNA synthetases revealed by their inhibition by analogues of a reaction intermediate, and by properties of truncated forms

2. A single amino acid substitution affects the substrate specificity of the seryl-tRNA synthetase homologue

3. 2-[2-Substituted-3-(3,4-dichlorobenzylamino)propylamino]-1H-quinolin-4-ones as Staphylococcus aureus methionyl-tRNA synthetase inhibitors

4. Synthetic Microcin C Analogs Targeting Different Aminoacyl-tRNA Synthetases

5. Inhibition of Helicobacter pylori aminoacyl-tRNA amidotransferase by chloramphenicol analogs

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