Back to Search Start Over

18-substituted steroids--Part 17. 2 alpha-hydroxylated liver metabolites of aldosterone identified by high-field [1H]NMR spectroscopy.

Authors :
Latif SA
Morris DJ
Wei L
Kirk DN
Burke PJ
Toms HC
Shackleton CH
Source :
Journal of steroid biochemistry [J Steroid Biochem] 1989 Dec; Vol. 33 (6), pp. 1119-25.
Publication Year :
1989

Abstract

11 beta,18-Epoxy-2 alpha,3 alpha,18,21-tetrahydroxy-5 alpha,17 alpha- pregnan-20-one (2 alpha-hydroxy-3 alpha,5 alpha-tetrahydro-17-isoaldosterone) and its apo isomer have been identified by high-field NMR studies, supported by thermospray HPLC/MS, to be among the major polar metabolites formed from incubation of aldosterone with rat liver microsomal fraction. Indications that unreduced 2 alpha-hydroxy-aldosterone is also present among the metabolites have still to be confirmed.

Details

Language :
English
ISSN :
0022-4731
Volume :
33
Issue :
6
Database :
MEDLINE
Journal :
Journal of steroid biochemistry
Publication Type :
Academic Journal
Accession number :
2615356
Full Text :
https://doi.org/10.1016/0022-4731(89)90418-4