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Flag Counter
  2. World Encyclopedia
  3. Dimethyldienolone
Dimethyldienolone
From Wikipedia, the free encyclopedia
Dimethyldienolone
Clinical data
Other namesRU-2788; 7α,17α-Dimethyldienolone; Δ9-Mibolerone; δ9-7α,17α-Dimethyl-19-nortestosterone; 7α,17α-Dimethylestr-4,9-dien-17β-ol-3-one
Drug classAndrogen; Anabolic steroid
Identifiers
CAS Number
PubChem CID
ChemSpider
UNII
Chemical and physical data
FormulaC20H28O2
Molar mass300.442 g·mol−1
3D model (JSmol)
  • C[C@@H]1CC2=CC(=O)CCC2=C3[C@@H]1[C@@H]4CC[C@]([C@]4(CC3)C)(C)O
  • InChI=1S/C20H28O2/c1-12-10-13-11-14(21)4-5-15(13)16-6-8-19(2)17(18(12)16)7-9-20(19,3)22/h11-12,17-18,22H,4-10H2,1-3H3/t12-,17+,18-,19+,20+/m1/s1
  • Key:NDTOIEPBCIVPTI-ZGPIAVDESA-N

Dimethyldienolone (developmental code name RU-2788), or 7α,17α-dimethyldienolone, also known as δ9-7α,17α-dimethyl-19-nortestosterone or as 7α,17α-dimethylestr-4,9-dien-17β-ol-3-one, is a 17α-alkylated androgen/anabolic steroid of the 19-nortestosterone group which was never marketed.[1][2] It is closely related to dimethyltrienolone, as well as to mibolerone and metribolone.[1][2] Dimethyldienolone shows high affinity for the androgen and progesterone receptors.[1][2]

Dimethyldienolone is made from almestrone.

See also

[edit]

References

[edit]
  1. ^ a b c Delettré J, Mornon JP, Lepicard G, Ojasoo T, Raynaud JP (January 1980). "Steroid flexibility and receptor specificity". J. Steroid Biochem. 13 (1): 45–59. doi:10.1016/0022-4731(80)90112-0. PMID 7382482.
  2. ^ a b c Ojasoo T, Delettré J, Mornon JP, Turpin-VanDycke C, Raynaud JP (1987). "Towards the mapping of the progesterone and androgen receptors". J. Steroid Biochem. 27 (1–3): 255–69. doi:10.1016/0022-4731(87)90317-7. PMID 3695484.



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Retrieved from "https://en.wikipedia.org/w/index.php?title=Dimethyldienolone&oldid=1336206880"
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