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Orestrate

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Orestrate
Clinical data
Other names17β-(Cyclohexen-1-yloxy)-estra-1,3,5(10)-trien-3-ol propionate
Identifiers
  • [(8R,9S,13S,14S,17S)-17-(Cyclohexen-1-yloxy)-13-methyl-6,7,8,9,11,12,14,15,16,17-decahydrocyclopenta[a]phenanthren-3-yl] propanoate
CAS Number
PubChem CID
ChemSpider
CompTox Dashboard (EPA)
Chemical and physical data
FormulaC27H36O3
Molar mass408.57294 g/mol g·mol−1
3D model (JSmol)
  • CCC(=O)OC1=CC2=C(C=C1)C3CCC4(C(C3CC2)CCC4OC5=CCCCC5)C
  • InChI=1S/C27H36O3/c1-3-26(28)30-20-10-12-21-18(17-20)9-11-23-22(21)15-16-27(2)24(23)13-14-25(27)29-19-7-5-4-6-8-19/h7,10,12,17,22-25H,3-6,8-9,11,13-16H2,1-2H3/t22-,23-,24+,25+,27+/m1/s1
  • Key:VYAXJSIVAVEVHF-RYIFMDQWSA-N

Orestrate (INN), also known as estradiol 3-propionate 17β-(1-cyclohexenyl) ether, is a synthetic, steroidal estrogen and estradiol ester that was never marketed.[1][2][3][4] It is the 3-propanoyl, 17-(1-cyclohexenyl) ether and ester of estradiol.[1][3]

References

  1. ^ a b J. Elks (14 November 2014). The Dictionary of Drugs: Chemical Data: Chemical Data, Structures and Bibliographies. Springer. pp. 898, 905. ISBN 978-1-4757-2085-3.
  2. ^ P. H. List; L. Hörhammer (12 March 2013). Chemikalien und Drogen Teil A: N-Q. Springer-Verlag. pp. 331–. ISBN 978-3-642-65035-2.
  3. ^ a b Edward B. Roche; Academy of Pharmaceutical Sciences. Medicinal Chemistry Section (1977). Design of biopharmaceutical properties through prodrugs and analogs: a symposium. The Academy. p. 7. ISBN 978-0-917330-16-2.
  4. ^ Galletti, F.; Gardi, R. (1974). "Effect of two orally active estradiol derivatives on sulfobromphthalein retention in rats". Pharmacological Research Communications. 6 (2): 135–145. doi:10.1016/S0031-6989(74)80021-4. ISSN 0031-6989.



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