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Methyldienolone

From Wikipedia, the free encyclopedia
Methyldienolone
Clinical data
Other namesRU-3467; 17α-Methylestra-4,9-dien-17β-ol-3-one
Routes of
administration
Oral
Legal status
Legal status
Identifiers
  • (8S,13S,14S,17S)-17-hydroxy-13,17-dimethyl-1,2,6,7,8,11,12,14,15,16-decahydrocyclopenta[a]phenanthren-3-one
CAS Number
ChemSpider
UNII
CompTox Dashboard (EPA)
Chemical and physical data
FormulaC19H26O2
Molar mass286.415 g·mol−1
3D model (JSmol)
  • O=C1C=C2C(=C3CC[C@]4(C)[C@@](C)(O)CC[C@H]4[C@@H]3CC2)CC1
  • InChI=1S/C19H26O2/c1-18-9-7-15-14-6-4-13(20)11-12(14)3-5-16(15)17(18)8-10-19(18,2)21/h11,16-17,21H,3-10H2,1-2H3/t16-,17+,18+,19+/m1/s1
  • Key:RDJBOAMEIJEKEY-XWSJACJDSA-N

Methyldienolone (developmental code name RU-3467), also known as 17α-methyl-19-nor-δ9-testosterone, as well as 17α-methylestra-4,9-dien-17β-ol-3-one, is a synthetic, orally active anabolic-androgenic steroid (AAS) and a 17α-alkylated derivative of 19-nortestosterone. It is closely related to dienolone and ethyldienolone.

Methyldienolone is on the World Anti-Doping Agency's list of prohibited substances,[1][2] and is therefore banned from use in most major sports.

See also

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References

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  1. ^ "The World Anti-Doping Code: The 2012 Prohibited List" (PDF). World Anti-Doping Agency. Archived from the original (PDF) on 2012-05-13. Retrieved 2012-07-17.
  2. ^ Joseph P, Dubey S, Ahi S, Bhasin N, Sharma PK, Pillai MG, Beotra A, Jain S, Taylor AM (2021). Investigating the Enhancement in Selectivity for the Analysis of Methyldienolone in Urine Samples by Differential Mobility Spectrometry (PDF). SCIEX technical note (Report).