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Organophosphate & Carbamate insecticides

Organophosphate and Carbamate insecticides are considerably less persistent and less lipophilic than the organochlorines, however they have a greater acute toxicity.

The organophosphate insecticides, comprised of esters of phosphoric and phosphorothioic acid, evolved from the chemical technology of the 1930s in which the nerve gases of World War II were developed. Both groups of compounds are neurotoxic, poisoning by inhibiting the enzyme acetylcholinesterase. By inhibiting cholinesterases, the accumulation of the important and widespread neurotransmitter acetylcholine occurs, resulting in later hyperstimulation of cholinergic pathways.

There are now over 200 organophosphate esters and 25 carbamate esters.

The basic "backbone" structures of the two types of anticholinesterase class insecticides, the organophosphorus and the carbamate esters.

(Amdur, Mary O., John Doull, and Curtis D. Klaassen. Toxicology, 1991, p. 580)

The interaction between an organophosphorus or carbamate ester with the serine hydroxyl group in the active site of the enzyme acetylcholinestrase.

(Amdur, Mary O., John Doull, and Curtis D. Klaassen. Toxicology, 1991, p. 585)

The basic structures and nomenclature of organophosphorus esthers.

(Amdur, Mary O., John Doull, and Curtis D. Klaassen. Toxicology, 1991, p. 583)

Kinetics of ester hydrolysis.

(Amdur, Mary O., John Doull, and Curtis D. Klaassen. Toxicology, 1991, p. 586)

Acetylcholine Events occuring at a chemical synapse in response to depolarization of teh axonal terminal.

(Marieb, Elaine N. Human Anatomy & Physiology, 1995, p. 362)

Signs and symptoms of anticholinesterase insecticide poisioning.

(Amdur, Mary O., John Doull, and Curtis D. Klaassen. Toxicology, 1991, p. 582)