Biotransformation of 17-alkyl steroids in the equine: high-performance liquid chromatography-mass spectrometric and gas chromatography-mass spectrometric analysis of fluoxymesterone metabolites in urine samples.
S M Stanley, S Kent, J P Rodgers
文献索引:J. Chromatogr. B. Biomed. Sci. Appl. 704 , 119, (1997)
全文:HTML全文
摘要
In this study the equine metabolism of fluoxymesterone (9alpha-fluoro-11beta-17beta-dihydroxy-17alpha-meth ylandrost-4-ene-3-one) given orally has been investigated. The parent material was not detected, but two major 16-hydroxy metabolites which corresponded to a mono- and a di-hydroxylation product were evident. One of the hydroxylation positions was identified as C-16. Phase II metabolism in the form of glucuronide formation was also common. These steroids will provide target compounds for confirming abuse of this drug in the horse.
相关化合物
相关文献:
1999-02-01
[Med. Sci Sports Exerc. 31 , 243, (1999)]
2000-01-01
[J. Clin. Oncol. 18(2) , 262-6, (2000)]
2001-02-28
[Stat. Med. 20(4) , 557-79, (2001)]
1995-08-01
[J. Pharmacol. Toxicol. Methods 33(4) , 187-95, (1995)]
2006-07-01
[Breast Cancer Res. Treat. 98(2) , 217-22, (2006)]