Identification of Butyrylcholinesterase Adducts after Inhibition with Isomalathion Using Mass Spectrometry: Difference in Mechanism between (1R)- and (1S)-Stereoisomers-Reference-Cited by-同舟云学术

Identification of Butyrylcholinesterase Adducts after Inhibition with Isomalathion Using Mass Spectrometry: Difference in Mechanism between (1R)- and (1S)-Stereoisomers

Published:2001-10 Issue:2 Volume:176 Page:73-80
ISSN:0041-008X
Container-title:Toxicology and Applied Pharmacology
language:en
Short-container-title:Toxicology and Applied Pharmacology

Author:

Doorn Jonathan A.,Schall Michael,Gage Douglas A.,Talley Todd T.,Thompson Charles M.,Richardson Rudy J.

Publisher

Elsevier BV

Subject

Pharmacology,Toxicology

Reference29 articles.

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4. Kinetics of the postinhibitory reactions of acetylcholinesterase poisoned by chiral isomalathion: A surprising nonreactivation induced by the RP stereoisomers;Berkman;Chem. Res. Toxicol.,1993

5. Synthesis, absolute configuration, and analysis of malathion, malaoxon, and isomalathion enantiomers;Berkman;Chem. Res. Toxicol.,1993

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