1989
DOI: 10.1002/bms.1200180612
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Studies on anabolic steroidsII—gas chromatographic/mass spectrometric characterization of oxandrolone urinary metabolites in man

Abstract: The metabolism of 17 alpha-methyl-17 beta-hydroxy-2-oxa-5 alpha-androstan-3-one (oxandrolone) in man has been investigated by gas chromatography/mass spectrometry. After oral administration of a 10 mg dose to man, five metabolites were detected in the free fraction of the urinary samples. Oxandrolone, the major compound excreted in urine, was detected within 72 h after administration. During this period 35.8 and 8.4% of the administered dose was excreted as unchanged oxandrolone and 17-epioxandrolone, respecti… Show more

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Cited by 35 publications
(20 citation statements)
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“…Consequently, trends in the comparison of the groups’ height velocity increment did not become statistically significant. Growth acceleration is comparable to previous reports on the use of testosterone [3, 4]or oxandrolone [5, 6, 7, 8, 9, 10]in CDG. Along with comparable growth, gonadarche advanced faster in the testosterone-50-mg group than in the oxandrolone group.…”
Section: Discussionsupporting
confidence: 77%
See 1 more Smart Citation
“…Consequently, trends in the comparison of the groups’ height velocity increment did not become statistically significant. Growth acceleration is comparable to previous reports on the use of testosterone [3, 4]or oxandrolone [5, 6, 7, 8, 9, 10]in CDG. Along with comparable growth, gonadarche advanced faster in the testosterone-50-mg group than in the oxandrolone group.…”
Section: Discussionsupporting
confidence: 77%
“…It is almost completely absorbed, reaches peak blood levels at 1 h and is eliminated with a half-life of 9.4 h [2]. In distinct contrast to testosterone, oxandrolone undergoes little metabolism or conjugation and is not aromatized into estrogen [3]. …”
Section: Introductionmentioning
confidence: 99%
“…Reduction of C-3 keto group and hydroxylation at C-6 position are also proposed. M7 concerns steroids with heteroatom at steroidal structure (as in oxandrolone molecule [20,21]) which directs metabolism to C-/D-rings leading to the 17-epimerized, 16-hydroxylated and dehydration products.…”
Section: Proposed Metabolism Scheme For Steroids With 5˛-androstan-3-mentioning
confidence: 99%
“…less than 5% for probenecid or 51% for ethamivan), their chromatographic behavior and/or instability of their derivatives (e.g. 17α‐epioxandrolone) 23. As explained before, extracts analysed by GC/MS/MS were prepared using the routine extraction procedure, just as those screened by conventional GC/MS 24, 25.…”
Section: Resultsmentioning
confidence: 99%