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
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
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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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