Synthesis, Bioactivity and SAR study of N′-(5-substituted-1,3,4-thiadiazol-2-yl)-N-cyclopropylformyl-thioureas as ketol-acid reductoisomerase Inhibitors-Reference-Cited by-同舟云学术

Synthesis, Bioactivity and SAR study of N′-(5-substituted-1,3,4-thiadiazol-2-yl)-N-cyclopropylformyl-thioureas as ketol-acid reductoisomerase Inhibitors

Published:2009-04-01 Issue:2 Volume:24 Page:545-552
ISSN:1475-6366
Container-title:Journal of Enzyme Inhibition and Medicinal Chemistry
language:en
Short-container-title:Journal of Enzyme Inhibition and Medicinal Chemistry

Author:

Liu Xing-Hai¹,Zhang Chuan-Yu¹,Guo Wan-Cheng¹,Li Yong-Hong¹,Chen Pei-Quan¹,Wang Teng²,Dong Wei-Li¹,Wang Bao-Lei¹,Sun Hong-Wei²,Li Zheng-Ming¹³

Affiliation:

1. 1State-Key Laboratory of Elemento-Organic Chemistry, Nankai University, Tianjin, China

2. 2Department of Chemistry, College of Chemistry, Nankai University, Tianjin, China

3. 3National Pesticide Engineering Research Center, Nankai University, Tianjin, 300071, China

Publisher

Informa UK Limited

Subject

Drug Discovery,Pharmacology,General Medicine

Link

https://www.tandfonline.com/doi/pdf/10.1080/14756360802234943

Reference25 articles.

1. Acetolactate Synthase Is the Site of Action of Two Sulfonylurea Herbicides in Higher Plants

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3. Enzymology, Structure, and Dynamics of Acetohydroxy Acid Isomeroreductase

4. The herbicidally active experimental compound Hoe 704 is a potent inhibitor of the enzyme acetolactate reductoisomerase

5. Oxalyl hydroxamates as reaction-intermediate analogs for ketol-acid reductoisomerase

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