1973
DOI: 10.1021/jf60190a046
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Metabolites and photoproducts of 3-(2-butyl)phenyl N-methylcarbamate and N-benzenesulfenyl-N-methylcarbamate

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Cited by 17 publications
(5 citation statements)
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“…b Relative Rf with benzene-ether (1:1), normalizing the Rf of BP (0.56) and BPMC (0.45) to 0.97 and the other products proportionately. The same Rf order is observed with etherhexane (2:1), benzene-ether (10:3), benzene-ether-hexane (1:1:1), and hexane-ether (2:1) (Cheng and Casida, 1973). i'-ch2oh-cob V~ch2oh-cob-I unknown Bassigned, on a tentative basis, by their relative Rf values, in comparison with authentic sec-butyl derivatives in two different series {Cheng and Casida, 1973; Table III).…”
Section: Metabolism Of [3h]cob and [3h]cb In Mouse Liversupporting
confidence: 70%
See 1 more Smart Citation
“…b Relative Rf with benzene-ether (1:1), normalizing the Rf of BP (0.56) and BPMC (0.45) to 0.97 and the other products proportionately. The same Rf order is observed with etherhexane (2:1), benzene-ether (10:3), benzene-ether-hexane (1:1:1), and hexane-ether (2:1) (Cheng and Casida, 1973). i'-ch2oh-cob V~ch2oh-cob-I unknown Bassigned, on a tentative basis, by their relative Rf values, in comparison with authentic sec-butyl derivatives in two different series {Cheng and Casida, 1973; Table III).…”
Section: Metabolism Of [3h]cob and [3h]cb In Mouse Liversupporting
confidence: 70%
“…The same Rf order is observed with etherhexane (2:1), benzene-ether (10:3), benzene-ether-hexane (1:1:1), and hexane-ether (2:1) (Cheng and Casida, 1973). i'-ch2oh-cob V~ch2oh-cob-I unknown Bassigned, on a tentative basis, by their relative Rf values, in comparison with authentic sec-butyl derivatives in two different series {Cheng and Casida, 1973; Table III). However, the possibility that either or both of these metabolites may be dihydroxy-COB derivatives cannot be unequivocally excluded.…”
Section: Metabolism Of [3h]cob and [3h]cb In Mouse Liversupporting
confidence: 70%
“…N-methylcarbamates (BPMC, MPMC, MTMC, NAC, and XMC) are metabolized by MFO, and their major metabolites show no or lower anti-AChE activity than the parent chemicals (Cheng and Casida, 1973;Miyamoto and Fukunaga, 1971;Ohkawa et al, 1974;Oonnithan and Casida, 1968). Takahashi and colleagues (1987) reported that treatment with fenitrothion increased plasma concentrations of other N-methylcarbamates more than those of BPMC, although the potentiation of BPMC toxicity was strongest.…”
Section: Potentiationmentioning
confidence: 99%
“…Cheng and Casida (59) studied the metabolism of Chevron RE 11775, 3-(2-butyl)-phenyl N-methylcarbamate. This paper is very detailed and discusses in depth the metabolic pathways of this compound.…”
Section: Carbamatesmentioning
confidence: 99%