Quinestradol

Quinestradol

Systematic (IUPAC) name
(8R,9S,13S,14S,16R,17R)-3-cyclopentyloxy-13-methyl-6,7,8,9,11,12,14,15,16,17-decahydrocyclopenta[a]phenanthrene-16,17-diol
Identifiers
CAS Number	1169-79-5
ATC code	None
PubChem	CID 14431
ChemSpider	16735993
Chemical data
Formula	C23H32O3
Molar mass	356.498 g/mol
SMILES CC12CCC3C(C1CC(C2O)O)CCC4=C3C=CC(=C4)OC5CCCC5
InChI InChI=1S/C23H32O3/c1-23-11-10-18-17-9-7-16(26-15-4-2-3-5-15)12-14(17)6-8-19(18)20(23)13-21(24)22(23)25/h7,9,12,15,18-22,24-25H,2-6,8,10-11,13H2,1H3/t18-,19-,20+,21-,22+,23+/m1/s1 Key:ODYKCPYPRCJXLY-PZORDLPLSA-N

Quinestradol (INN, BAN) (brand names Colpovis, Colpovister, Pentovis), or quinestradiol, also known as estriol 3-cyclopentyl ether, is a synthetic estrogen which is no longer used clinically.^[1][2][3][4] It has been studied in the treatment of stress incontinence in elderly women with efficacy observed.^[3][4]

See also

• Nilestriol
• Estradiol cypionate
• Estriol
• Ethinyl estradiol
• Quinestrol
• Quingestanol
• Quingestanol acetate

References

1. J. Elks (14 November 2014). The Dictionary of Drugs: Chemical Data: Chemical Data, Structures and Bibliographies. Springer. pp. 899–. ISBN 978-1-4757-2085-3.
2. Index Nominum 2000: International Drug Directory. Taylor & Francis. January 2000. pp. 905–. ISBN 978-3-88763-075-1.
3. P.G. Crosignani; Rodolfo Paoletti; P.M. Sarrel; N.K. Wenger (6 December 2012). Women’s Health in Menopause: Behaviour, Cancer, Cardiovascular Disease, Hormone Replacement Therapy. Springer Science & Business Media. pp. 245–. ISBN 978-94-011-1024-2.
4. David B. Seifer (27 July 1999). Menopause: Endocrinology and Management. Springer Science & Business Media. pp. 161–. ISBN 978-1-59259-246-3.