Synthesis of [7-3H]-3β, 16β-dihydoxy-5-androsten-17-one
✍ Scribed by Ronald B. Franklin; Randolph J. McMurtry; Sidney D. Nelson
- Publisher
- John Wiley and Sons
- Year
- 1981
- Tongue
- French
- Weight
- 352 KB
- Volume
- 18
- Category
- Article
- ISSN
- 0022-2135
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
A method has been described for the synthesis of tritiated [7‐^3^H]‐3β,16β‐dihydroxy‐5‐androsten‐17‐one of high specific activity starting from [7‐^3^H]‐5‐androsten‐17‐one. The identity of the radioactive steroid was established by thin layer chromato‐graphy, gas chromatography and gas chromatography combined with mass spectroscopy. The radiolabelled steroid may be used to study its disposition and metabolism in experimental animals and also to further investigate the potential role of 3β,16β‐dihydroxy‐5‐androsten‐17‐one in patients with low renin essential hypertension.
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## Abstract Die Bereitung des 3β‐Acetoxy‐14, 16α‐dihydroxy‐5β, 14β, 17 βH‐ätiansäure‐methylesters wird beschrieben. Damit sind, was die Asymmetriezentren an C‐16 und C‐17 betrifft, alle 4 Stereoisomeren dieses Esters bekannt.