Year |
Citation |
Score |
2021 |
Crawford RA, Bowman KR, Cagle BS, Doorn JA. In vitro inhibition of glutathione-S-transferase by dopamine and its metabolites, 3,4-dihydroxyphenylacetaldehyde and 3,4-dihydroxyphenylacetic acid. Neurotoxicology. PMID 34314733 DOI: 10.1016/j.neuro.2021.07.005 |
0.316 |
|
2010 |
Allen EM, Anderson DG, Florang VR, Khanna M, Hurley TD, Doorn JA. Relative inhibitory potency of molinate and metabolites with aldehyde dehydrogenase 2: implications for the mechanism of enzyme inhibition. Chemical Research in Toxicology. 23: 1843-50. PMID 20954713 DOI: 10.1021/Tx100317Q |
0.325 |
|
2006 |
Doorn JA, Hurley TD, Petersen DR. Inhibition of human mitochondrial aldehyde dehydrogenase by 4-hydroxynon-2-enal and 4-oxonon-2-enal. Chemical Research in Toxicology. 19: 102-10. PMID 16411662 DOI: 10.1021/Tx0501839 |
0.327 |
|
2003 |
Doorn JA, Thompson CM, Christner RB, Richardson RJ. Stereoselective inactivation of Torpedo californica acetylcholinesterase by isomalathion: inhibitory reactions with (1R)- and (1S)-isomers proceed by different mechanisms. Chemical Research in Toxicology. 16: 958-65. PMID 12924923 DOI: 10.1021/Tx030026E |
0.638 |
|
2001 |
Doorn JA, Schall M, Gage DA, Talley TT, Thompson CM, Richardson RJ. Identification of butyrylcholinesterase adducts after inhibition with isomalathion using mass spectrometry: difference in mechanism between (1R)- and (1S)-stereoisomers. Toxicology and Applied Pharmacology. 176: 73-80. PMID 11601883 DOI: 10.1006/Taap.2001.9279 |
0.634 |
|
2001 |
Doorn JA, Talley TT, Thompson CM, Richardson RJ. Probing the active sites of butyrylcholinesterase and cholesterol esterase with isomalathion: conserved stereoselective inactivation of serine hydrolases structurally related to acetylcholinesterase. Chemical Research in Toxicology. 14: 807-13. PMID 11453726 DOI: 10.1021/Tx015501S |
0.623 |
|
2000 |
Doorn JA, Gage DA, Schall M, Talley TT, Thompson CM, Richardson RJ. Inhibition of acetylcholinesterase by (1S,3S)-isomalathion proceeds with loss of thiomethyl: kinetic and mass spectral evidence for an unexpected primary leaving group. Chemical Research in Toxicology. 13: 1313-20. PMID 11123973 DOI: 10.1021/Tx000184V |
0.634 |
|
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