Nicotinoid Insecticides and the Nicotinic Acetylcholine ReceptorI. Yamamoto, J.E. Casida Insect pest control has continuously evolved from inorganics to botanicals, to chlo- rinated hydrocarbons, to organophosphorus compounds and methylcarbamates, then synthetic pyrethroids and most recently synthetic nicotinoids as the major classes. These insecticides allowed high standards of crop protection at minimal cost. A limitation in each new class of compounds is the selection of resistant strains and ultimate control failures and this serves as a driving force to discover and develop replacement compounds to circumvent resistance and overcome problem areas. The nicotinoids now play a critical role in meeting this need. Three generations of chemicals are involved in the history of nicotinoid insecti- cides. The first generation was the botanical nicotine used for at least three centuries to control sucking insect pests but largely replaced in the 1940s and 1950s by the more effective organophosphorus compounds and methylcarbamates, some with systemic properties. Synthesis programs based on nicotine as a prototype did not yield compounds that could compete with other synthetic insecticides. The second generation was the nitromethylene type such as nithiazine, discovered by Shell sci- entists in a screening/optimization program. The nitromethylenes had the potency, selectivity, and systemic properties but lacked the field effectiveness largely because of photolability (so close yet so far from a major commercial product). The third generation required a series of advances made by Bayer researchers starting from nithiazine as the model and enhancing its photostability and potency with a nitroimine and chloropyridyl moiety, respectively, to give imidacloprid, the subject of much of this monograph. |
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Contents
Nicotine to Nicotinoids 1962 to 1997 | 3 |
Nicotine and Other Insecticidal Alkaloids | 29 |
Discovery of the Nitromethylene Heterocycle Insecticides | 71 |
Discovery of Chloronicotinyl Insecticides | 91 |
Chloronicotinyl Insecticides A Success of the New Chemistry | 109 |
Discovery of a New Systemic Insecticide Nitenpyram and Its Insecticidal Properties | 127 |
A Novel Insecticide Acetamiprid | 149 |
CGA 293343 A Novel BroadSpectrum Neonicotinoid Insecticide | 177 |
Imidacloprid Toxicology and Metabolism | 213 |
10 The Action of Nicotine in the Mammalian Brain | 223 |
Nicotine Analogs StructureAffinity Relationships For Central Nicotinic Acetylcholinergic Receptor Binding | 237 |
Managing Resistance to the Chloronicotinyi Insecticides Rhetoric or Reality? | 253 |
Structure and Function of Insect Nicotinic Acetylcholine Receptors Studied with Nicotinoid Insecticide Affinity Probes | 271 |
293 | |
Other editions - View all
Nicotinoid Insecticides and the Nicotinic Acetylcholine Receptor I. Yamamoto,J.E. Casida Limited preview - 2012 |
Nicotinoid Insecticides and the Nicotinic Acetylcholine Receptor I. Yamamoto,J.E. Casida No preview available - 2013 |
Common terms and phrases
acetamiprid action affinity agents alkaloids analogs aphid application atom beetle binding Biochem biological brain brown planthopper Casida central channel Chem chemical chemistry chloronicotinyl cholinergic compared compounds concentrations cotton Crop derivatives dose Drosophila effect efficacy et al field Figure foliar formulation functional heterocyclic higher highly imidacloprid important increased indicate insect insecticidal activity isolated labeled laboratory larvae lead leaves ligands major method mg/kg mode of action moiety nAChR natural neonicotinoids neuronal nicotinic acetylcholine receptor nicotinoids nitenpyram nithiazine nitrogen nitromethylene novel observed Pestic Sci Pesticide pests plant population position potato potential practical prepared properties Protection rates recently relationships relatively resistance respectively rice ring seed selective showed shown soil species spray strains structure studies substituents subunits synthesis synthetic Table tobacco Tomizawa toxicity treatment values whitefly Yamamoto