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161 related items for PubMed ID: 1763518
1. Quinine is a more potent inhibitor than quinidine in rat of the oxidative metabolic routes of methoxyphenamine which involve debrisoquine 4-hydroxylase. Muralidharan G, Hawes EM, McKay G, Midha KK. Xenobiotica; 1991 Nov; 21(11):1441-50. PubMed ID: 1763518 [Abstract] [Full Text] [Related]
3. Selective in vivo inhibition by quinidine of methoxyphenamine oxidation in rat models of human debrisoquine polymorphism. Muralidharan G, Midha KK, McKay G, Hawes EM, Inaba T. Xenobiotica; 1989 Feb; 19(2):189-97. PubMed ID: 2786289 [Abstract] [Full Text] [Related]
4. Metabolism of methoxyphenamine in vitro by a CYP2D6 microsomal preparation. Coutts RT, Bolaji OO, Su P, Baker GB. Drug Metab Dispos; 1994 Feb; 22(5):756-60. PubMed ID: 7835228 [Abstract] [Full Text] [Related]
15. Oxidation of reduced haloperidol to haloperidol: involvement of human P450IID6 (sparteine/debrisoquine monooxygenase). Tyndale RF, Kalow W, Inaba T. Br J Clin Pharmacol; 1991 Jun; 31(6):655-60. PubMed ID: 1867960 [Abstract] [Full Text] [Related]
16. An evaluation of cytochrome P450 isoform activities in the female dark agouti (DA) rat: relevance to its use as a model of the CYP2D6 poor metaboliser phenotype. Barham HM, Lennard MS, Tucker GT. Biochem Pharmacol; 1994 Apr 20; 47(8):1295-307. PubMed ID: 8185638 [Abstract] [Full Text] [Related]
17. Methoxyphenamine metabolism in rat models of human debrisoquine phenotypes. Roy SD, Hawes EM, McKay G, Hubbard JW, Midha KK. Can J Physiol Pharmacol; 1985 Jul 20; 63(7):778-81. PubMed ID: 3876145 [Abstract] [Full Text] [Related]
18. Neuronal cytochrome P450IID1 (debrisoquine/sparteine-type): potent inhibition of activity by (-)-cocaine and nucleotide sequence identity to human hepatic P450 gene CYP2D6. Tyndale RF, Sunahara R, Inaba T, Kalow W, Gonzalez FJ, Niznik HB. Mol Pharmacol; 1991 Jul 20; 40(1):63-8. PubMed ID: 1857341 [Abstract] [Full Text] [Related]