Biosynthesis of estrogens. Estr-5(10)-ene-3,17-dione: isolation, metabolism and mechanistic implications
Author:
Publisher
Royal Society of Chemistry (RSC)
Link
http://pubs.rsc.org/en/content/articlepdf/1993/P1/P19930001529
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3. Mechanistic studies on C-19 demethylation in oestrogen biosynthesis
4. Hydroperoxides as inactivators of aromatase: 10.beta.-hydroperoxy-4-estrene-3,17-dione, crystal structure and inactivation characteristics
5. Aromatization of tetralone derivatives by 5,10,15,20-tetrakis(pentafluorophenyl)porphyrinatoiron(III) chloride/iodosobenzene and cytochrome P-450cam: a model study on aromatase cytochrome P-450 reaction
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1. A three-step synthesis of estra-4,9-diene-3,17-dione;Canadian Journal of Chemistry;2019-04
2. Steroidal Estrogens;Estrogens and Antiestrogens I;1999
3. The impact of aromatase mechanism on other P450s;The Journal of Steroid Biochemistry and Molecular Biology;1997-04
4. Model Studies on Heme Monooxygenases;Catalysis by Metal Complexes;1997
5. Mechanistic kinship between hydroxylation and desaturation reactions: acyl-carbon bond cleavage promoted by pig and human CYP17 (P-45017.alpha.; 17.alpha.-hydroxylase-17,20-lyase);Biochemistry;1995-10-01
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