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Ethyltestosterone

From Wikipedia, the free encyclopedia
Synthetic anabolic steroid
Pharmaceutical compound
Ethyltestosterone
Clinical data
Other names17α-Ethyltestosterone; 17α-Ethylandrost-4-en-17β-ol-3-one; 17α-Pregn-4-en-17-ol-3-one
Routes of
administration
By mouth
Identifiers
  • (8R,9S,10R,13S,14S,17S)-17-ethyl-17-hydroxy-10,13-dimethyl-2,6,7,8,9,11,12,14,15,16-decahydro-1H-cyclopenta[a]phenanthren-3-one
CAS Number
PubChemCID
ChemSpider
UNII
ChEMBL
CompTox Dashboard(EPA)
Chemical and physical data
FormulaC21H32O2
Molar mass316.485 g·mol−1
3D model (JSmol)
  • CC[C@@]1(CC[C@@H]2[C@@]1(CC[C@H]3[C@H]2CCC4=CC(=O)CC[C@]34C)C)O
  • InChI=1S/C21H32O2/c1-4-21(23)12-9-18-16-6-5-14-13-15(22)7-10-19(14,2)17(16)8-11-20(18,21)3/h13,16-18,23H,4-12H2,1-3H3/t16-,17+,18+,19+,20+,21+/m1/s1
  • Key:FGPGANCDNDLUST-CEGNMAFCSA-N

Ethyltestosterone, or17α-ethyltestosterone, also known as17α-ethylandrost-4-en-17β-ol-3-one or17α-pregn-4-en-17-ol-3-one, is asynthetic,orally activeanabolic–androgenic steroid (AAS) of the17α-alkylated group related tomethyltestosterone which was never marketed.[1][2] Like methyltestosterone, ethyltestosterone is theparent compound of many AAS.[3] Derivatives of ethyltestosterone includenorethandrolone (ethylnandrolone, ethylestrenolone),ethylestrenol (ethylnandrol),norboletone,ethyldienolone,tetrahydrogestrinone,bolenol (ethylnorandrostenol), andpropetandrol.[3]

Ethyltestosterone is described as a very weak AAS[4][5] and is considerably weaker as an AAS than is methyltestosterone.[6] It is reported to have 1/10 of theanabolicpotency and 1/20 of theandrogenic potency oftestosterone propionate in rodents.[7] Ethyltestosterone was also inactive in boys withdwarfism at 20 to 40 mg/dayorally.[7] The low potency of ethyltestosterone is in notable contrast tonorethandrolone (17α-ethyl-19-nortestosterone), the C19 nor analogue.[4]Analogues of ethyltestosterone with longer C17αchains such aspropyltestosterone (topterone) have further reduced androgenic activity or evenantiandrogenic activity.[2][8] In contrast to ethyltestosterone, its 19-demethyl variant, norethandrolone, is a potent AAS comparable inanabolic activity totestosterone propionate.[5]

See also

[edit]

References

[edit]
  1. ^Hill RA, Makin HL, Kirk DN, Murphy GM (23 May 1991).Dictionary of Steroids. CRC Press. pp. 423–.ISBN 978-0-412-27060-4.
  2. ^abSaunders FJ, Drill VA (May 1956). "The myotrophic and androgenic effects of 17-ethyl-19-nortestosterone and related compounds".Endocrinology.58 (5):567–572.doi:10.1210/endo-58-5-567.PMID 13317831.
  3. ^abShahidi NT (September 2001). "A review of the chemistry, biological action, and clinical applications of anabolic-androgenic steroids".Clinical Therapeutics.23 (9):1355–1390.doi:10.1016/s0149-2918(01)80114-4.PMID 11589254.
  4. ^abCamerino B, Sala G (1960). "Anabolic Steroids".Fortschritte der Arzneimittelforschung / Progress in Drug Research / Progrès des recherches pharmaceutiques. Vol. 2. Birkhäuser. pp. 71–134.doi:10.1007/978-3-0348-7038-2_2.ISBN 978-3-0348-7040-5.PMID 14448579.{{cite book}}:ISBN / Date incompatibility (help);|journal= ignored (help)
  5. ^abColton FB, Nysted LN, Riegel B, Raymond AL (1957). "17-Alkyl-19-nortestosterones".Journal of the American Chemical Society.79 (5):1123–1127.Bibcode:1957JAChS..79.1123C.doi:10.1021/ja01562a028.ISSN 0002-7863.
  6. ^Rangaswami S, Seshadri TR (1952).Chemistry of vitamins and hormones. Andhra Univ.
  7. ^abSchedl HP, Delea C, Bartter FC (August 1959). "Structure-activity relationships of anabolic steroids: role of the 19-methyl group".The Journal of Clinical Endocrinology and Metabolism.19 (8):921–935.doi:10.1210/jcem-19-8-921.PMID 14442516.
  8. ^Singh SM, Gauthier S, Labrie F (February 2000). "Androgen receptor antagonists (antiandrogens): structure-activity relationships".Current Medicinal Chemistry.7 (2):211–247.doi:10.2174/0929867003375371.PMID 10637363.
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