Dydrogesterone metabolism in human liver by aldo-keto reductases and cytochrome P450 enzymes
Author:
Affiliation:
1. Abbott Laboratories GmbH, Hannover, Germany and
2. Abbott Healthcare Products B.V, Weesp, the Netherlands
Publisher
Informa UK Limited
Subject
Health, Toxicology and Mutagenesis,Pharmacology,Toxicology,Biochemistry,General Medicine
Link
https://www.tandfonline.com/doi/pdf/10.3109/00498254.2015.1134852
Reference15 articles.
1. Progestins as inhibitors of the human 20-ketosteroid reductases, AKR1C1 and AKR1C3
2. Expression of human aldo-keto reductase 1C2 in cell lines of peritoneal endometriosis: Potential implications in metabolism of progesterone and dydrogesterone and inhibition by progestins
3. Clinical Significance of the Cytochrome P450 2C19 Genetic Polymorphism
4. Stereospecific reduction of 5β-reduced steroids by human ketosteroid reductases of the AKR (aldo-keto reductase) superfamily: role of AKR1C1–AKR1C4 in the metabolism of testosterone and progesterone via the 5β-reductase pathway
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1. Metabolism of progestogens used for contraception and menopausal hormone therapy;Steroids;2024-07
2. Lack of analytical interference of dydrogesterone in progesterone immunoassays;Clinical Chemistry and Laboratory Medicine (CCLM);2022-05-11
3. Dydrogesterone and 20α-dihydrodydrogesterone plasma levels on day of embryo transfer and clinical outcome in an anovulatory programmed frozen-thawed embryo transfer cycle: a prospective cohort study;Human Reproduction;2022-03-22
4. The other side of progestins: effects in the brain;Journal of Molecular Endocrinology;2016-08
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