Exploration of the structure–activity relationship and druggability of novel oxazolidinone‐based compounds as Gram‐negative antibacterial agents-Reference-Cited by-同舟云学术

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Exploration of the structure–activity relationship and druggability of novel oxazolidinone‐based compounds as Gram‐negative antibacterial agents

Published:2019-09-03 Issue:11 Volume:352 Page:1900129
ISSN:0365-6233
Container-title:Archiv der Pharmazie
language:en
Short-container-title:Arch Pharm Chem Life Sci

Author:

Ding Shi¹²,Ji Jing‐Chao¹,Zhang Ming‐Juan¹,Yang Yu‐She²,Wang Rui³,Zhu Xing‐Long¹,Wang Li‐Hong¹,Zhong Yi¹,Gao Le¹,Lu Man¹,Liu Ju¹^ORCID,Chen Ye¹

Affiliation:

1. Key Laboratory of New Drug Research and Development of Liaoning Province, College of Pharmacy Liaoning University Shenyang Liaoning China

2. State Key Laboratory of Drug Research, Shanghai Institute of Materia Medica Chinese Academy of Sciences Shanghai China

3. Central Hospital affiliated to Shenyang Medical College Shenyang Liaoning China

Funder

National Natural Science Foundation of China

Publisher

Wiley

Subject

Drug Discovery,Pharmaceutical Science

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/ardp.201900129

Reference16 articles.

1. Newer antibacterial drugs for a new century

2. Antibacterial Agents That Inhibit Lipid A Biosynthesis

3. Crystal structure of LpxC, a zinc-dependent deacetylase essential for endotoxin biosynthesis

4. Structure of the LpxC deacetylase with a bound substrate-analog inhibitor

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3. Oxazolidinones: Are they only good for the discovery of antibiotics? A worm's eye view;Journal of Molecular Structure;2023-08

4. Bacterial Zinc Metalloenzyme Inhibitors: Recent Advances and Future Perspectives;Molecules;2023-05-27

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