INHIBITION OF ETHINYLESTRADIOL AND TOLBUTAMIDE METABOLISM BY QUINOLINE DERIVATIVES INVITRO

被引：19

作者：

RIVIERE, JH ^{[1
]}

BACK, DJ ^{[1
]}

机构：

[1] UNIV LIVERPOOL, DEPT PHARMACOL & THERAPEUT, POB 147, LIVERPOOL L69 3BX, ENGLAND

来源：

CHEMICO-BIOLOGICAL INTERACTIONS | 1986年 / 59卷 / 03期

关键词：

D O I：

10.1016/S0009-2797(86)80075-8

中图分类号：

Q5 [生物化学]; Q7 [分子生物学];

学科分类号：

071010 ; 081704 ;

摘要：

引用

页码：301 / 308

页数：8

共 16 条

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[2] TOLBUTAMIDE AS A MODEL-DRUG FOR THE STUDY OF ENZYME-INDUCTION AND ENZYME-INHIBITION IN THE RAT [J].

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[3] INHIBITION OF DRUG-METABOLISM BY THE ANTI-MALARIAL DRUGS CHLOROQUINE AND PRIMAQUINE IN THE RAT [J].

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[4] EFFECTS OF INSECTICIDE SYNERGISTS ON MICROSOMAL OXIDATION OF ESTRADIOL AND ETHYNYLESTRADIOL AND ON MICROSOMAL DRUG-METABOLISM [J].

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[5] INTERINDIVIDUAL VARIATIONS IN DRUG DISPOSITION - CLINICAL IMPLICATIONS AND METHODS OF INVESTIGATION [J].

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[6] ON THE MECHANISM FOR THE RED-CELL ACCUMULATION OF MEFLOQUINE, AN ANTIMALARIAL DRUG [J].

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[7] HUMAN-LIVER CYTOCHROMES-P-450 INVOLVED IN POLYMORPHISMS OF DRUG OXIDATION [J].

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[8]

JENNER P, 1983, DRUG METAB DISPOS, P12

[9]

LOWRY OH, 1951, J BIOL CHEM, V193, P265

[10] THE BIOTRANSFORMATION OF 17-ALPHA-ETHYNYL[H-3]ESTRADIOL IN THE RAT - IRREVERSIBLE BINDING AND BILIARY METABOLITES [J].

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