Back to Search
Start Over
Structural Biology-Guided Design, Synthesis, and Biological Evaluation of Novel Insect Nicotinic Acetylcholine Receptor Orthosteric Modulators.
- Source :
-
Journal of medicinal chemistry [J Med Chem] 2022 Feb 10; Vol. 65 (3), pp. 2297-2312. Date of Electronic Publication: 2022 Jan 05. - Publication Year :
- 2022
-
Abstract
- The development of novel and safe insecticides remains an important need for a growing world population to protect crops and animal and human health. New chemotypes modulating the insect nicotinic acetylcholine receptors have been recently brought to the agricultural market, yet with limited understanding of their molecular interactions at their target receptor. Herein, we disclose the first crystal structures of these insecticides, namely, sulfoxaflor, flupyradifurone, triflumezopyrim, flupyrimin, and the experimental compound, dicloromezotiaz, in a double-mutated acetylcholine-binding protein which mimics the insect-ion-channel orthosteric site. Enabled by these findings, we discovered novel pharmacophores with a related mode of action, and we describe herein their design, synthesis, and biological evaluation.
- Subjects :
- 4-Butyrolactone analogs & derivatives
4-Butyrolactone chemistry
4-Butyrolactone metabolism
Animals
Binding Sites
Coleoptera drug effects
Coleoptera metabolism
Crystallography, X-Ray
Humans
Insect Control methods
Insect Proteins chemistry
Insect Proteins genetics
Insecticides metabolism
Insecticides pharmacology
Molecular Conformation
Molecular Dynamics Simulation
Mutagenesis, Site-Directed
Pyridines chemistry
Pyridines metabolism
Pyrimidinones chemistry
Pyrimidinones metabolism
Receptors, Nicotinic chemistry
Receptors, Nicotinic genetics
Sulfur Compounds chemistry
Sulfur Compounds metabolism
Drug Design
Insect Proteins metabolism
Insecticides chemical synthesis
Receptors, Nicotinic metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 1520-4804
- Volume :
- 65
- Issue :
- 3
- Database :
- MEDLINE
- Journal :
- Journal of medicinal chemistry
- Publication Type :
- Academic Journal
- Accession number :
- 34986308
- Full Text :
- https://doi.org/10.1021/acs.jmedchem.1c01767