Design, synthesis, and structure–activity relationships of pyrazole derivatives as potential FabH inhibitors-Reference-Cited by-同舟云学术

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Design, synthesis, and structure–activity relationships of pyrazole derivatives as potential FabH inhibitors

Published:2010-08 Issue:15 Volume:20 Page:4657-4660
ISSN:0960-894X
Container-title:Bioorganic & Medicinal Chemistry Letters
language:en
Short-container-title:Bioorganic & Medicinal Chemistry Letters

Author:

Lv Peng-Cheng,Sun Juan,Luo Yin,Yang Ying,Zhu Hai-Liang

Funder

National Natural Science Foundation of China

Jiangsu National Science Foundation

Anhui National Science Foundation

Publisher

Elsevier BV

Subject

Organic Chemistry,Clinical Biochemistry,Drug Discovery,Pharmaceutical Science,Molecular Biology,Molecular Medicine,Biochemistry

Reference27 articles.

1. Escherichia coli and Salmonella typhimurium;Cronan,1996

2. Bacterial β-ketoacyl-Acyl Carrier Protein Synthases as Targets for Antibacterial Agents

3. The Claisen condensation in biology

4. Isolation and characterization of the beta-ketoacyl-acyl carrier protein synthase III gene (fabH) from Escherichia coli K-12.

5. Purification and characterization of 3-ketoacyl-acyl carrier protein synthase III from spinach. A condensing enzyme utilizing acetyl-coenzyme A to initiate fatty acid synthesis.

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