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Methyl-1-testosterone - Wikipedia Jump to content

Methyl-1-testosterone

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Methyl-1-testosterone
Clinical data
Other namesM1T; SC-11195; Methyldihydroboldenone; 17αあるふぁ-Methyl-1-testosterone; 17αあるふぁ-Methyl-4,5αあるふぁ-dihydro-δでるた1-testosterone; 17αあるふぁ-Methyl-δでるた1-DHT; 17αあるふぁ-Methyl-5αあるふぁ-androst-1-en-17βべーた-ol-3-one
Routes of
administration
By mouth
Identifiers
  • (5S,8R,9S,10R,13S,14S,17S)-17-hydroxy-10,13,17-trimethyl-5,6,7,8,9,11,12,14,15,16-decahydro-4H-cyclopenta[a]phenanthren-3-one
CAS Number
PubChem CID
ChemSpider
UNII
CompTox Dashboard (EPA)
ECHA InfoCard100.219.594 Edit this at Wikidata
Chemical and physical data
FormulaC20H30O2
Molar mass302.458 g·mol−1
3D model (JSmol)
  • O=C4\C=C/[C@]1([C@@H](CC[C@@H]2[C@@H]1CC[C@]3([C@H]2CC[C@@]3(O)C)C)C4)C
  • InChI=1S/C20H30O2/c1-18-9-6-14(21)12-13(18)4-5-15-16(18)7-10-19(2)17(15)8-11-20(19,3)22/h6,9,13,15-17,22H,4-5,7-8,10-12H2,1-3H3/t13-,15+,16-,17-,18-,19-,20-/m0/s1
  • Key:JRNSSSJKIGAFCT-YDSAWKJFSA-N

Methyl-1-testosterone (M1T; developmental code name SC-11195), also known as 17αあるふぁ-methyl-4,5αあるふぁ-dihydro-δでるた1-testosterone (17αあるふぁ-methyl-δでるた1-DHT) or 17αあるふぁ-methyl-5αあるふぁ-androst-1-en-17βべーた-ol-3-one, as well as methyldihydroboldenone, is a synthetic and orally active anabolic–androgenic steroid (AAS)[1] which was never marketed for medical use. It is the 17αあるふぁ-methyl derivative of 1-testosterone (Δでるた1-DHT; dihydroboldenone).

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

References

[edit]
  1. ^ Parr MK, Blatt C, Zierau O, Hess C, Gütschow M, Fusshöller G, Opfermann G, Schänzer W, Diel P (December 2011). "Endocrine characterization of the designer steroid methyl-1-testosterone: investigations on tissue-specific anabolic-androgenic potency, side effects, and metabolism". Endocrinology. 152 (12): 4718–28. doi:10.1210/en.2011-1164. PMID 21990312.
  2. ^ "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.