128 related articles for article (PubMed ID: 11123973)
1. Inhibition of acetylcholinesterase by (1S,3S)-isomalathion proceeds with loss of thiomethyl: kinetic and mass spectral evidence for an unexpected primary leaving group.
Doorn JA; Gage DA; Schall M; Talley TT; Thompson CM; Richardson RJ
Chem Res Toxicol; 2000 Dec; 13(12):1313-20. PubMed ID: 11123973
[TBL] [Abstract][Full Text] [Related]
2. Kinetic evidence for different mechanisms of acetylcholinesterase inhibition by (1R)- and (1S)-stereoisomers of isomalathion.
Jianmongkol S; Marable BR; Berkman CE; Talley TT; Thompson CM; Richardson RJ
Toxicol Appl Pharmacol; 1999 Feb; 155(1):43-53. PubMed ID: 10036217
[TBL] [Abstract][Full Text] [Related]
3. Identification of butyrylcholinesterase adducts after inhibition with isomalathion using mass spectrometry: difference in mechanism between (1R)- and (1S)-stereoisomers.
Doorn JA; Schall M; Gage DA; Talley TT; Thompson CM; Richardson RJ
Toxicol Appl Pharmacol; 2001 Oct; 176(2):73-80. PubMed ID: 11601883
[TBL] [Abstract][Full Text] [Related]
4. Probing the active sites of butyrylcholinesterase and cholesterol esterase with isomalathion: conserved stereoselective inactivation of serine hydrolases structurally related to acetylcholinesterase.
Doorn JA; Talley TT; Thompson CM; Richardson RJ
Chem Res Toxicol; 2001 Jul; 14(7):807-13. PubMed ID: 11453726
[TBL] [Abstract][Full Text] [Related]
5. Stereoselective inactivation of Torpedo californica acetylcholinesterase by isomalathion: inhibitory reactions with (1R)- and (1S)-isomers proceed by different mechanisms.
Doorn JA; Thompson CM; Christner RB; Richardson RJ
Chem Res Toxicol; 2003 Aug; 16(8):958-65. PubMed ID: 12924923
[TBL] [Abstract][Full Text] [Related]
6. Inhibition of Acetylcholinesterases by Stereoisomeric Organophosphorus Compounds Containing Both Thioester and
Talley TT; Chao CK; Berkman CE; Richardson RJ; Thompson CM
Chem Res Toxicol; 2020 Sep; 33(9):2455-2466. PubMed ID: 32833441
[TBL] [Abstract][Full Text] [Related]
7. Relative potencies of the four stereoisomers of isomalathion for inhibition of hen brain acetylcholinesterase and neurotoxic esterase in vitro.
Jianmongkol S; Berkman CE; Thompson CM; Richardson RJ
Toxicol Appl Pharmacol; 1996 Aug; 139(2):342-8. PubMed ID: 8806851
[TBL] [Abstract][Full Text] [Related]
8. Kinetics of the postinhibitory reactions of acetylcholinesterase poisoned by chiral isomalathion: a surprising nonreactivation induced by the RP stereoisomers.
Berkman CE; Ryu S; Quinn DA; Thompson CM
Chem Res Toxicol; 1993; 6(1):28-32. PubMed ID: 8448346
[TBL] [Abstract][Full Text] [Related]
9. Interaction of acetylcholinesterase with the enantiomers of malaoxon and isomalathion.
Berkman CE; Quinn DA; Thompson CM
Chem Res Toxicol; 1993; 6(5):724-30. PubMed ID: 8292752
[TBL] [Abstract][Full Text] [Related]
10. Resolving pathways of interaction of mipafox and a sarin analog with human acetylcholinesterase by kinetics, mass spectrometry and molecular modeling approaches.
Mangas I; Taylor P; Vilanova E; Estévez J; França TC; Komives E; Radić Z
Arch Toxicol; 2016 Mar; 90(3):603-16. PubMed ID: 25743373
[TBL] [Abstract][Full Text] [Related]
11. Effects of cyclodextrin on the stereoselectivity inhibition of acetylcholinesterase by isomalathion.
Sun JQ; Tao NE; Zhang AP; Qi H
J Environ Sci Health B; 2018; 53(9):580-586. PubMed ID: 29842826
[TBL] [Abstract][Full Text] [Related]
12. Enantioselective interaction of acid α-naphthyl acetate esterase with chiral organophosphorus insecticides.
Zhang A; Sun J; Lin C; Hu X; Liu W
J Agric Food Chem; 2014 Feb; 62(7):1477-81. PubMed ID: 24475784
[TBL] [Abstract][Full Text] [Related]
13. Inhibition of AChE by malathion and some structurally similar compounds.
Krstić DZ; Colović M; Kralj MB; Franko M; Krinulović K; Trebse P; Vasić V
J Enzyme Inhib Med Chem; 2008 Aug; 23(4):562-73. PubMed ID: 18608787
[TBL] [Abstract][Full Text] [Related]
14. Aging pathways for organophosphate-inhibited human butyrylcholinesterase, including novel pathways for isomalathion, resolved by mass spectrometry.
Li H; Schopfer LM; Nachon F; Froment MT; Masson P; Lockridge O
Toxicol Sci; 2007 Nov; 100(1):136-45. PubMed ID: 17698511
[TBL] [Abstract][Full Text] [Related]
15. Resolving pathways of interaction of covalent inhibitors with the active site of acetylcholinesterases: MALDI-TOF/MS analysis of various nerve agent phosphyl adducts.
Elhanany E; Ordentlich A; Dgany O; Kaplan D; Segall Y; Barak R; Velan B; Shafferman A
Chem Res Toxicol; 2001 Jul; 14(7):912-8. PubMed ID: 11453739
[TBL] [Abstract][Full Text] [Related]
16. Aging of mipafox-inhibited human acetylcholinesterase proceeds by displacement of both isopropylamine groups to yield a phosphate adduct.
Kropp TJ; Richardson RJ
Chem Res Toxicol; 2006 Feb; 19(2):334-9. PubMed ID: 16485911
[TBL] [Abstract][Full Text] [Related]
17. Inhibition of AChE by single and simultaneous exposure to malathion and its degradation products.
Krstić D; Colović M; Krinulović K; Djurić D; Vasić V
Gen Physiol Biophys; 2007 Dec; 26(4):247-53. PubMed ID: 18281741
[TBL] [Abstract][Full Text] [Related]
18. Direct analysis of the kinetic profiles of organophosphate-acetylcholinesterase adducts by MALDI-TOF mass spectrometry.
Jennings LL; Malecki M; Komives EA; Taylor P
Biochemistry; 2003 Sep; 42(37):11083-91. PubMed ID: 12974645
[TBL] [Abstract][Full Text] [Related]
19. Novel Organophosphate Ligand O-(2-Fluoroethyl)-O-(p-Nitrophenyl)Methylphosphonate: Synthesis, Hydrolytic Stability and Analysis of the Inhibition and Reactivation of Cholinesterases.
Chao CK; Ahmed SK; Gerdes JM; Thompson CM
Chem Res Toxicol; 2016 Nov; 29(11):1810-1817. PubMed ID: 27551891
[TBL] [Abstract][Full Text] [Related]
20. Assisted inhibition effect of acetylcholinesterase with n-octylphosphonic acid and application in high sensitive detection of organophosphorous pesticides by matrix-assisted laser desorption/ionization Fourier transform mass spectrometry.
Cai T; Zhang L; Wang H; Zhang J; Guo Y
Anal Chim Acta; 2011 Nov; 706(2):291-6. PubMed ID: 22023864
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]