18-Substituted steroids. Part 15. 6 beta-Hydroxylation of aldosterone by liver

6 beta-Hydroxyaldosterone and 6 beta-hydroxy-17-isoaldosterone, characterized by high-field NMR studies, are among the major polar metabolites formed from aldosterone by incubation with rat liver slices or microsomal fraction. It is uncertain at present whether the 17-iso product results from an enz...

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Veröffentlicht in:Steroids 1989-08, Vol.54 (2), p.169-184
Hauptverfasser: Kirk, D N, Burke, P J, Toms, H C, Latif, S A, Morris, D J
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container_title Steroids
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creator Kirk, D N
Burke, P J
Toms, H C
Latif, S A
Morris, D J
description 6 beta-Hydroxyaldosterone and 6 beta-hydroxy-17-isoaldosterone, characterized by high-field NMR studies, are among the major polar metabolites formed from aldosterone by incubation with rat liver slices or microsomal fraction. It is uncertain at present whether the 17-iso product results from an enzymatic or a chemical inversion of configuration. Periodate degradation of the 6 beta-hydroxyaldosterone gave 6 beta-hydroxyaldosterone gamma-lactone, identical with a synthetic sample.
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source Elsevier ScienceDirect Journals Complete - AutoHoldings; MEDLINE
subjects Aldosterone - analogs & derivatives
Aldosterone - chemical synthesis
Aldosterone - metabolism
Animals
Chemical Phenomena
Chemistry
Chromatography, High Pressure Liquid
Hydroxylation
Hydroxyprogesterones - analysis
In Vitro Techniques
Liver - metabolism
Magnetic Resonance Spectroscopy
Male
Rats
Rats, Inbred Strains
Spectrophotometry, Ultraviolet
title 18-Substituted steroids. Part 15. 6 beta-Hydroxylation of aldosterone by liver
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