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Ethyldienolone

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Ethyldienolone
Skeletal formula of ethyldienolone
Ball-and-stick model of the ethyldienolone molecule
Clinical data
Other names17α-Methyl-19-nor-δ9-testosterone; 17α-Methylestra-4,9-dien-17β-ol-3-one
Routes of
administration		By mouth
Identifiers
  • (8S,13S,14S,17S)-17-ethyl-17-hydroxy-13-methyl-1,2,6,7,8,11,12,14,15,16-decahydrocyclopenta[a]phenanthren-3-one
PubChem CID
ChemSpider
UNII
CompTox Dashboard (EPA)
Chemical and physical data
FormulaC20H28O2
Molar mass300.442 g·mol−1
3D model (JSmol)
  • CC[C@@]1(CC[C@@H]2[C@@H]1CCC3=C4CCC(=O)C=C4CC[C@@H]23)O
  • InChI=1S/C19H26O2/c1-2-19(21)10-9-17-16-5-3-12-11-13(20)4-6-14(12)15(16)7-8-18(17)19/h11,16-18,21H,2-10H2,1H3/t16-,17+,18+,19+/m1/s1
  • Key:MPJHQVVZUHVQJF-XWSJACJDSA-N
 ☒NcheckY (what is this?)  (verify)

Ethyldienolone, also known as 17α-methyl-19-nor-δ9-testosterone, as well as 17α-methylestra-4,9-dien-17β-ol-3-one, is synthetic, orally active anabolic-androgenic steroid (AAS) and a 17α-alkylated derivative of 19-nortestosterone. It is slightly more active than methyltestosterone when given orally.[1] Ethyldienolone is closely related to dienolone and methyldienolone.

See also

References

  1. ^ Edgren RA, Peterson DL, Jones RC, Nagra CL, Smith H, Hughes GA (1966). "Biological effects of synthetic gonanes". Recent Progress in Hormone Research. 22: 305–49. doi:10.1016/b978-1-4831-9825-5.50011-7. ISBN 978-1-4831-9825-5. PMID 5334628.
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