Chemical preparation, degradation analysis, computational docking and biological activities of novel sulfonylureas with 2,5-disubstituted groups
- 13 October 2022
- journal article
- research article
- Published by Elsevier in Pesticide Biochemistry and Physiology
- Vol. 188, 105261
Abstract
No abstract availableKeywords
Funding Information
- National Key Research and Development Program of China (2021YFD1700103)
- National Natural Science Foundation of China (21977057, 22277060)
- Ministry of Science and Technology of the People's Republic of China
This publication has 22 references indexed in Scilit:
- Resistance to AHAS inhibitor herbicides: current understandingPest Management Science, 2013
- Synthesis and evaluation of novel monosubstituted sulfonylurea derivatives as antituberculosis agentsEuropean Journal of Medicinal Chemistry, 2012
- A very simple and highly efficient procedure for N-formylation of primary and secondary amines at room temperature under solvent-free conditionsTetrahedron Letters, 2010
- A short history of SHELXActa Crystallographica Section A Foundations of Crystallography, 2007
- Herbicide-binding sites revealed in the structure of plant acetohydroxyacid synthaseProceedings of the National Academy of Sciences, 2006
- Abiotic Degradation of Iodosulfuron-methyl-ester in Aqueous SolutionJournal of Agricultural and Food Chemistry, 2005
- Expression, purification and characterization of Arabidopsis thaliana acetohydroxyacid synthaseBiochemical Journal, 1997
- LIGPLOT: a program to generate schematic diagrams of protein-ligand interactionsProtein Engineering, Design and Selection, 1995
- Site of Action of ChlorsulfuronPlant Physiology, 1984
- Acetolactate Synthase Is the Site of Action of Two Sulfonylurea Herbicides in Higher PlantsScience, 1984