Oral contraceptives as substrates and inhibitors for human cytosolic SULTs

Journal of Biochemistry

Volumn 137, Issue 3, 2005, Pages 401-406

  Yasuda, Shin ^a   Suiko, Masahito ^a   Liu, Ming Cheh ^a  

^a UNIVERSITY OF TEXAS HEALTH CENTER   (United States)

Author keywords

17 ethynylestradiol; 17 estradiol; Contraceptive; Phenol sulfotransferase; Sulfation

Indexed keywords

19 NORETHINDRONE; ESTRADIOL; ESTRONE; ETHINYLESTRADIOL; ETYNODIOL DIACETATE; LEVONORGESTREL; MEDROXYPROGESTERONE; MESTRANOL; MIFEPRISTONE; NORETHISTERONE ACETATE; ORAL CONTRACEPTIVE AGENT; SULFOTRANSFERASE; UNCLASSIFIED DRUG;

ARTICLE; CONTROLLED STUDY; CYTOSOL; DRUG EFFECT; DRUG INHIBITION; DRUG MECHANISM; DRUG METABOLISM; DRUG SULFATION; ENZYME KINETICS; ENZYME SPECIFICITY; HEPATOMA CELL; HOMEOSTASIS; HUMAN; HUMAN CELL; IC 50; IN VIVO STUDY;

ARYLSULFOTRANSFERASE; CARCINOMA, HEPATOCELLULAR; CELL LINE, TUMOR; CONTRACEPTIVES, ORAL; CYTOSOL; ESTRADIOL; ETHYNODIOL DIACETATE; HUMANS; KINETICS; MIFEPRISTONE; NORETHINDRONE;

MAMMALIA;

EID: 18244393185     PISSN: 0021924X     EISSN: None     Source Type: Journal    
DOI: 10.1093/jb/mvi047     Document Type: Article

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