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Glucuronidation of the steroid enantiomers ent-17β-estradiol, ent-androsterone and ent-etiocholanolone by the human UDP-glucuronosyltransferases

✍ Scribed by Nina Sneitz; Kathiresan Krishnan; Douglas F. Covey; Moshe Finel


Book ID
116698719
Publisher
Elsevier Science
Year
2011
Tongue
English
Weight
466 KB
Volume
127
Category
Article
ISSN
0960-0760

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Hydroxyl groups at C-3 and at C-17 of th
✍ Dai Kitamoto; Serge Dieth; Alain Burger; Denis Tritsch; Jean-François Biellmann 📂 Article 📅 2001 🏛 Elsevier Science 🌐 French ⚖ 72 KB

## The ent-androsta-4,9(11)-diene-3b,17b-diol 1b and ent-androsta-5,9(11)-diene-3b,17b -diol 2b prepared from chiral dione 3, were oxidised by cholesterol oxidase with kinetic parameters close to those of the natural steroids 1a and 2a. In the preparative oxidation the final product was ent-andros