intoxicant.wiki2catechol4school
Compound

Penmesterol

Original Wikipedia articleen.wikipedia.org/wiki/Penmesterol revision used (24 October 2026)

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Overview

Penmesterol (INN (International Nonproprietary Name)) (brand names Pandrocine, Testopan; former developmental code name RP-12222), or penmestrol, also known as 17α-methyltestosterone 3-cyclopentyl enol ether, is a synthetic, orally active anabolic-androgenic steroid (AAS) that was developed in the early 1960s. It is the 3-cyclopentyl enol ether of methyltestosterone.[1–7] WP

Chemistry

Formula
C25H38O2 PC
CAS number
67-81-2 PC
Molar mass (g/mol)
370.6 PC
IUPAC name (computed by PubChem)
(8R,9S,10R,13S,14S,17S)-3-cyclopentyloxy-10,13,17-trimethyl-1,2,7,8,9,11,12,14,15,16-decahydrocyclopenta[a]phenanthren-17-ol PC
SMILES
C[C@]12CCC(=CC1=CC[C@@H]3[C@@H]2CC[C@]4([C@H]3CC[C@]4(C)O)C)OC5CCCC5 PC
InChIKey
ZUBDXGHKAAMAAA-RFXJPFPRSA-N PC
PubChem CID
20054971

Harm reduction information

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Sources

  1. Other Negwer M, Scharnow HG. Organic-chemical drugs and their synonyms: (an international survey). 4 October 2001
  2. Other Elks J. The Dictionary of Drugs: Chemical Data: Chemical Data, Structures and Bibliographies. 14 November 2014
  3. Other Azziz, Ricardo. Androgen Excess Disorders in Women. 8 November 2007
  4. Other Sittig M, William Andrew Publishing. Pharmaceutical Manufacturing Encyclopedia, 3rd Edition. 22 October 2013
  5. Other List PH, Hörhammer L. Chemikalien und Drogen Teil A: N-Q. 12 March 2013
  6. Journal / agency Ercoli A, Gardi R. Δ4-3-Keto Steroidal Enol Ethers. Paradoxical Dependency of Their Effectiveness on the Administration Route. Journal of the American Chemical Society. 1960. doi:10.1021/ja01488a062
  7. Other Wermuth CG. The Practice of Medicinal Chemistry. 2 May 2011

Text and values on this page are quoted from Wikipedia (CC BY-SA 4.0), PubChem (public domain). Each value links to the exact revision it came from.