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Nat Prod Res ; 18(6): 529-35, 2004 Dec.
Article in English | MEDLINE | ID: mdl-15595610

ABSTRACT

Fermentation of (+)-androst-4-ene-3,17-dione (1) with Curvularia lunata for 10 days yielded five oxidative and reductive metabolites, androsta-1,4-diene-3,17-dione (2), 17beta-hydroxyandrosta-1,4-dien-3-one (3), 11alpha-hydroxyandrost-4-ene-3,17-dione (4), 11alpha,17beta-dihydroxyandrost-4-en-3-one (5) and 15alpha-hydroxyandrosta-1,4-dien-17-one (6). The structures of these metabolites were elucidated on the basis of spectroscopic techniques. These microbially transformed products were assayed against the clinically important enzymes, tyrosinase and prolyl endopeptidase.


Subject(s)
Androstenedione/pharmacokinetics , Ascomycota/metabolism , Phytotherapy , Androstenedione/administration & dosage , Androstenedione/chemistry , Animals , Biotransformation , Fermentation , Humans , Magnetic Resonance Spectroscopy , Plant Extracts/administration & dosage , Plant Extracts/chemistry , Plant Extracts/pharmacokinetics
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