Tigestol
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Formula | C20H28O |
Molar mass | 284.443 g·mol−1 |
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Tigestol (INN, USAN), also known as 17α-ethynylestr-5(10)-en-17β-ol,[1] is a steroidal progestin of the 19-nortestosterone group that was developed by Organon in the 1960s but was never marketed.[2][3][4][5] It is an isomer of the related 19-nortestosterone derivative progestins lynestrenol and cingestol.[6]
References
- ^ List PH, Hörhammer L (12 March 2013). Chemikalien und Drogen Teil C: T–Z. Springer-Verlag. pp. 179–. ISBN 978-3-642-67085-5.
- ^ Hill RA, Makin HL, Kirk DN, Murphy GM (23 May 1991). Dictionary of Steroids. CRC Press. pp. 424–. ISBN 978-0-412-27060-4.
- ^ United States Adopted Names (USAN). United States Pharmacopeial Convention. 1969. p. 65,85.
- ^ Lednicer D, Mitscher LA (13 May 1980). The Organic Chemistry of Drug Synthesis. John Wiley & Sons. pp. 145–. ISBN 978-0-471-04392-8.
- ^ Lednicer D (1998). Strategies for Organic Drug Synthesis and Design. Wiley. p. 95. ISBN 978-0-471-19657-0.
- ^ GB 841411, "New 19-Nor-Steroid Compounds and process for the preparation thereof", published 1960-07-13, assigned to Organon Laboratories Ltd.