Cytochrome P-450 metabolic-intermediate complex formation with a series of diphenhydramine analogues
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[1] J. Noordhoek,et al. Effect of multiple administration of orphenadrine or mono-N-desmethylorphenadrine on cytochrome P-450 catalyzed reactions in the rat , 1983, Archives of Toxicology.
[2] D. Pessayre,et al. Formation of an inactive cytochrome P-450Fe(II)-metabolite complex after administration of amiodarone in rats, mice and hamsters. , 1986, Biochemical pharmacology.
[3] B. Lindeke,et al. CYTOCHROME P-450 COMPLEX FORMATION IN THE METABOLISM OF PHENYLALKYLAMINES. 8. TEREOSELECTIVITY IN METABOLIC INTERMEDIARY COMPLEX FORMATION WITH A SERI S OF CHIRAL 2-SUBSTITUTED 1-PHENYL-2-AMINOETHANES , 1984 .
[4] J. Noordhoek,et al. Relationship Between Molecular Structure and Cytochrome P450−Metabolic Intermediate Complex Formation , 1984 .
[5] K. Jönsson,et al. Cytochrome P-455 nm complex formation in the metabolism of phenylalkylamines. 8. Stereoselectivity in metabolic intermediary complex formation with a series of chiral 2-substituted 1-phenyl-2-aminoethanes. , 1984, Journal of medicinal chemistry.
[6] J. Noordhoek,et al. Product inhibition in orphenadrine metabolism as a result of a stable cytochrome P-450-metabolic intermediate complex formed during the disposition of mono-N-desmethylorphenadrine (tofenacine) in the rat. , 1983, Research communications in chemical pathology and pharmacology.
[7] D. Pessayre,et al. Formation of inactive cytochrome P-450 Fe(II)-metabolite complexes with several erythromycin derivatives but not with josamycin and midecamycin in rats. , 1983, Biochemical pharmacology.
[8] L. Pershing,et al. Cytochrome P-450 metabolic-intermediate complex formation and induction by macrolide antibiotics; a new class of agents. , 1982, Xenobiotica; the fate of foreign compounds in biological systems.
[9] J. Noordhoek,et al. Spectral interaction of orphenadrine and its metabolites with oxidized and reduced hepatic microsomal cytochrome P-450 in the rat. , 1982, Biochemical pharmacology.
[10] C. Wolf,et al. Quantitation of two forms of pulmonary cytochrome P-450 in microsomes, using substrate specificities. , 1980, Molecular pharmacology.
[11] Rf Rekker,et al. THE HYDROPHOBIC FRAGMENTAL CONSTANT; AN EXTENSION TO A 1000 DATA POINT SET , 1979 .
[12] S. Orrenius,et al. Cytochrome P450 product complexes and glutathione consumption produced in isolated hepatocytes by norbenzphetamine and its N-oxidized congeners. , 1979, Biochemical pharmacology.
[13] M. Franklin. Inhibition of mixed-function oxidations by substrates forming reduced cytochrome P-450 metabolic-intermediate complexes , 1977 .
[14] C. Hansch. Quantitative Relationships Between Lipophilic Character and Drug Metabolism , 1972 .