Menthofuran (II, 4,5,6,7-tetrahydro-3,6-dimethyl benzofuran), the proximate toxin of R-(+)-pulegone (I), was administered orally to rats (200 mg/kg of body weight/day) for three days and the urinary metabolites were investigated. Among the several metabolites formed, two of them viz. 4-Hydroxy-4-methyl-2-cyclohexenone (VII) and p-cresol (VIII) were indentified. In support of the formation of these metabolites, it has been demonstrated that phenobarbital induced rat liver microsomes readily convert 4-methyl-2-cyclohexenone (V) to 4-hydroxy-4-methyl-2-cyclohexenone (VII) and p-cresol (VIII) in the presence of NADPH and O2. Possible mechanism for the formation of these two metabolites (VII, VIII) from menthofuran (II) has been proposed
Oral administration (250 mg/kg) of menthofuran, a monoterpene furan, to rats once daily for 3 days c...
The toxicological effects of p-cresol have primarily been attributed to its metabolism products; how...
Metabolic disposition of 5,5-dimethyl-2-(1-methylethylidene)-cyclohexanone (I) was examined in rats....
Menthofuran (II, 4,5,6,7-tetrahydro-3,6-dimethyl benzofuran), the proximate toxin of R-(+)-pulegone ...
Metabolic fate of menthofuran (II) in rats was investigated. Menthofuran (II) was administered orall...
Incubation of R-(+)-pulegone(I) with PB-induced rat liver microsomes in the presence of NADPH result...
1. S -(-)-pulegone was administered orally to rat (250 mg kg) and the nature of the urinary metaboli...
1. The metabolic disposition of R-(+)-pulegone (1) was examined in rats following four daily oral do...
It was shown earlier that the monoterpene ketone, piperitenone (I) is one of the major metabolites o...
1. The metabolic disposition of R-(+)-pulegone (1) was examined in rats following four daily oral do...
R-(+)-Pulegone was administered orally to rats and the urinary metabolites were investigated. Six me...
1. R-(+)-Pulegone was administered orally to rats and the urinary metabolites were investigated. Six...
R-(+)-Pulegone, a monoterpene ketone, is a potent hepatotoxin. One of the major metabolites of puleg...
It was shown earlier that the monoterpene ketone, piperitenone (I) is one of the major metabolites o...
Metabolism of l-menthol in rats was investigated both in vivo and in vitro. Metabolites isolated and...
Oral administration (250 mg/kg) of menthofuran, a monoterpene furan, to rats once daily for 3 days c...
The toxicological effects of p-cresol have primarily been attributed to its metabolism products; how...
Metabolic disposition of 5,5-dimethyl-2-(1-methylethylidene)-cyclohexanone (I) was examined in rats....
Menthofuran (II, 4,5,6,7-tetrahydro-3,6-dimethyl benzofuran), the proximate toxin of R-(+)-pulegone ...
Metabolic fate of menthofuran (II) in rats was investigated. Menthofuran (II) was administered orall...
Incubation of R-(+)-pulegone(I) with PB-induced rat liver microsomes in the presence of NADPH result...
1. S -(-)-pulegone was administered orally to rat (250 mg kg) and the nature of the urinary metaboli...
1. The metabolic disposition of R-(+)-pulegone (1) was examined in rats following four daily oral do...
It was shown earlier that the monoterpene ketone, piperitenone (I) is one of the major metabolites o...
1. The metabolic disposition of R-(+)-pulegone (1) was examined in rats following four daily oral do...
R-(+)-Pulegone was administered orally to rats and the urinary metabolites were investigated. Six me...
1. R-(+)-Pulegone was administered orally to rats and the urinary metabolites were investigated. Six...
R-(+)-Pulegone, a monoterpene ketone, is a potent hepatotoxin. One of the major metabolites of puleg...
It was shown earlier that the monoterpene ketone, piperitenone (I) is one of the major metabolites o...
Metabolism of l-menthol in rats was investigated both in vivo and in vitro. Metabolites isolated and...
Oral administration (250 mg/kg) of menthofuran, a monoterpene furan, to rats once daily for 3 days c...
The toxicological effects of p-cresol have primarily been attributed to its metabolism products; how...
Metabolic disposition of 5,5-dimethyl-2-(1-methylethylidene)-cyclohexanone (I) was examined in rats....