Structure–activity relationships of synthetic progestins in a yeast-based in vitro androgen bioassay
The recent identification of tetrahydrogestrinone (THG), a non-marketed designer androgen used for sports doping but previously undetectable by established mass spectrometry-based urine drug screens, and its production by a facile chemical modification of gestrinone has raised concerns about the ris...
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Veröffentlicht in: | The Journal of steroid biochemistry and molecular biology 2008-05, Vol.110 (1), p.39-47 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | The recent identification of tetrahydrogestrinone (THG), a non-marketed designer androgen used for sports doping but previously undetectable by established mass spectrometry-based urine drug screens, and its production by a facile chemical modification of gestrinone has raised concerns about the risks of developing designer androgens from numerous marketed progestins. We therefore have used yeast-based
in vitro androgen and progesterone bioassays to conduct a structure–activity study assessing the intrinsic androgenic potential of commercially available progestins and their derivatives, to identify those compounds or structures with the highest risk of forming a basis for such misapplication. Progestins had a wide range of androgenic bioactivity that was not reliably predicted for individual steroids by their progestin bioactivity. 17α-Hydroxyprogesterone and 19-norprogesterone derivatives with their bulky 17β-substituents were strong progestins but generally weak androgens. 17α-Ethynylated derivatives of testosterone, 19-nortestosterone and 18-methyl-19-nortestosterone such as gestrinone, ethisterone, norethisterone and norgestrel had the most significant intrinsic androgenicity of all the commercially marketed progestins. Facile chemical modification of the 17α-ethynyl group of each of these progestins produces 17α-methyl, ethyl and allyl derivatives, including THG and norbolethone, which further enhanced androgenic bioactivity. Thus by using the rapid and sensitive yeast bioassay we have screened a comprehensive set of progestins and associated structures and identified the ethynylated testosterone, 19-nortestosterone and 18-methyl-19-nortestosterone derivatives as possessing the highest risk for abuse and potential for conversion to still more potent androgens. By contrast, modern progestins such as progesterone, 17α-hydroxyprogesterone and 19-norprogesterone derivatives had minimal androgenic bioactivity and pose low risk. |
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ISSN: | 0960-0760 1879-1220 |
DOI: | 10.1016/j.jsbmb.2007.10.008 |