Quingestanol
Part of the metabolic pathway of Quingestanol. See the timeline on the metabolic highway.
Overview
Quingestanol (INN (International Nonproprietary Name), BAN (British Approved Name)), also known as norethisterone 3-cyclopentyl enol ether, is a progestin of the 19-nortestosterone group which was never marketed. It is a prodrug of norethisterone. An acylated derivative, quingestanol acetate, is used as a pharmaceutical drug.[1]
Chemistry
- Formula
- C25H34O2 PC
- CAS number
- 10592-65-1 PC
- Molar mass (g/mol)
- 366.5 PC
- IUPAC name (computed by PubChem)
- (8R,
9S, PC10R, 13S, 14S, 17R) - 3- cyclopentyloxy- 17- ethynyl- 13- methyl- 2, 7, 8, 9, 10, 11, 12, 14, 15, 16- decahydro- 1H- cyclopenta[a] phenanthren- 17- ol - SMILES
- C[C@]
12CC[C@@H] PC3[C@H] 4CCC(=CC4=CC[C@H] 3[C@@H] 1CC[C@] 2(C#C) O) OC5CCCC5 - InChIKey
- PCJFRMOEZQQSAX-
AIOSZGMZSA- PCN - PubChem CID
- 9842127
Harm reduction information
No harm reduction data is on file for this compound yet. That means no dose, timing or combination data from PsychonautWiki or TripSit. Please don't guess a dose from similar compounds. If you have taken it and feel unwell, contact emergency services or a poison control center.
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Sources
- Other Macdonald F. Dictionary of Pharmacological Agents. 1997
- Journal / agency Raynaud JP, Ojasoo T. The design and use of sex-steroid antagonists. J. Steroid Biochem. 1986. doi:10.1016/0022-4731(86)90313-4 · PMID 3543501
- Journal / agency Di Carlo FJ, Loo JC, Aceto T, Zuleski FR, Barr WH. Quingestanol acetate metabolism in women. Pharmacology. 1974. doi:10.1159/000136501 · PMID 4853997
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.