Table 1

Inhibition of coumarin 7-hydroxylase activity of CYP2A6 by organosulfur compounds

ChemicalsResidual Activity
1 μM10 μM
%
Dimethyl sulfide95.798.4
Dimethyl disulfide93.794.1
Diethyl sulfide93.689.4
Diethyl disulfide99.279.6
Di-n-propyl sulfide96.983.4
Di-n-propyl disulfide85.039.5
Di-n-butyl sulfide10082.0
Di-n-butyl disulfide87.543.9
Di-n-amyl sulfide10388.8
Di-n-amyl disulfide10066.3
Diallyl sulfide97.291.3
Diallyl disulfide89.746.2
Allyl methyl sulfide99.897.6
Allyl n-propyl sulfide10294.2
Allyl phenyl sulfide84.732.8
Diphenyl sulfide84.746.1
Diphenyl disulfide97.565.7
Phenyl cyclopropyl sulfide98.042.1
Difurfuryl disulfide94.169.1
2,2′-Dipyridyl disulfide98.797.0
4,4′-Dipyridyl sulfide20.63.22
4,4′-Dipyridyl disulfide15.92.26
Tranylcypromine48.912.9
SM-1250298.185.9
(−)-Nicotine10498.1
(−)-Cotinine10196.2

Concentration of coumarin was 2.5 μM. The control activity of CYP2A6 determined in the absence of an organosulfur compound was 3.76 nmol/min/nmol of CYP.