Jump to content

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
UNII
Chemical and physical data
FormulaC20H28O2
Molar mass300.442 g·mol−1
3D model (JSmol)
  • O([H])[C@](C)1CC[C@]([H])2[C@@]([H])3[C@](C)CC4=CC(CCC4=C3CC[C@@]21C)=O
  • InChI=1S/C20H27O2/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/h11,17-18,22H,4-10H2,1-3H3/t17-,18+,19-,20-/m0/s1
  • Key:IMHVOBKUZQVUFU-YRPNKDGESA-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]

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.



pFad - Phonifier reborn

Pfad - The Proxy pFad of © 2024 Garber Painting. All rights reserved.

Note: This service is not intended for secure transactions such as banking, social media, email, or purchasing. Use at your own risk. We assume no liability whatsoever for broken pages.


Alternative Proxies:

Alternative Proxy

pFad Proxy

pFad v3 Proxy

pFad v4 Proxy