BRAIN CORTEX;
CATALEPSY;
CONFERENCE PAPER;
DRUG ACTIVATION;
DRUG HYDROXYLATION;
DRUG MECHANISM;
DRUG METABOLISM;
DRUG OXIDATION;
DRUG RECEPTOR BINDING;
DRUG TOLERANCE;
DRUG TRANSFORMATION;
HUMAN;
HYPOTHERMIA;
LIVER MICROSOME;
NONHUMAN;
Howlett, A. C., Bonner, T. I., Cabral, G. A., Casellas, P., Devane, W. A., Felder, C. C., Herkenham, M., Martin, B. R., Mechoulam, R., Pertwee, R. G. (1998). The IUPHAR Receptor Compendium of Receptor Characterization and Classification, Cannabinoid Receptors. IUPHAR Media, pp. 97-104.
Structure of a cannabinoid receptor and functional expression of the cloned cDNA
Matsuda, L. A., Lolait, S. J., Brownstein, B. J., Young, A. C., Bonner, T. L. (1990). Structure of a cannabinoid receptor and functional expression of the cloned cDNA. Nature 346:561-564.
cDNA cloning and sequence of CYP2C29 encoding P450MUT-2, a microsomal aldehyde oxygenase
Matsunaga, T., Watanabe, K., Yamamoto, I., Negishi, M., Gonzalez, F. J., Yoshimura, H. (1994). cDNA cloning and sequence of CYP2C29 encoding P450MUT-2, a microsomal aldehyde oxygenase. Biochim. Biophys. Acta 1184:299-301.
Oxygenation mechanism in conversion of aldehyde to carboxylic acid catalyzed by a cytochrome P-450 isozyme
Watanabe, K., Narimatsu, S., Yamamoto, I., Yoshimura, H. (1991). Oxygenation mechanism in conversion of aldehyde to carboxylic acid catalyzed by a cytochrome P-450 isozyme. J. Biol. Chem. 266:2709-2711.
A cytochrome P450 isozyme having aldehyde oxygenase activity plays a major role in metabolizing cannabinoids by mouse hepatic microsomes
Watanabe, K., Narimatsu, S., Matsunaga, T., Yamamoto, I., Yoshimura, H. (1993). A cytochrome P450 isozyme having aldehyde oxygenase activity plays a major role in metabolizing cannabinoids by mouse hepatic microsomes. Biochem. Pharmacol. 46:405-411.
Involvement of CYP2C in the metabolism of cannabinoids by human hepatic microsomes from an old woman
Watanabe, K., Matsunaga, T., Yamamoto, I., Funae, Y., Yoshimura, H. (1995). Involvement of CYP2C in the metabolism of cannabinoids by human hepatic microsomes from an old woman. Biol. Pharm. Bull. 18:1138-1141.
Novel drug metabolizing enzymes identified from cannabinoid metabolic studies, and their reaction mechanisms
Yamamoto, I. (1999). Novel drug metabolizing enzymes identified from cannabinoid metabolic studies, and their reaction mechanisms (review). Xenobiotic Metab. Dispos. 14:111-119.
The pharmacological activity of cannabinol and its major metabolite, 11-hydroxycannabinol
Yamamoto, I., Watanabe, K., Kuzuoka, K., Narimatsu, S., Yoshimura, H. (1987). The pharmacological activity of cannabinol and its major metabolite, 11-hydroxycannabinol. Chem. Pharm. Bull. 35:2144-2147.
Oxygenation mechanism in the oxidation of xenobiotic aldehyde to carboxylic acid by mouse hepatic microsomes
Yamamoto, I., Watanabe, K., Narimatsu, S., Yoshimura, H. (1988). Oxygenation mechanism in the oxidation of xenobiotic aldehyde to carboxylic acid by mouse hepatic microsomes. Biochem. Biophys. Res. Commun. 153:779-782.
A novel metabolite, an oxepin formed from cannabidiol with guinea pig hepatic microsomes
Yamamoto, I., Nagai, K., Watanabe, K., Matsunaga, T., Yoshimura, H. (1995a). A novel metabolite, an oxepin formed from cannabidiol with guinea pig hepatic microsomes. J. Pharm. Pharmacol. 47:683-686.
Yamamoto, I., Watanabe, K., Narimatsu, S., Yoshimura, H. (1995b). Recent advances in the metabolism of cannabinoids (review). Int. J. Biochem. Cell Biol. 27:741-746.