Misplaced Pages

Tosagestin

Article snapshot taken from Wikipedia with creative commons attribution-sharealike license. Give it a read and then ask your questions in the chat. We can research this topic together.
Chemical compound Not to be confused with Tocogest or Tocogestan. Pharmaceutical compound
Tosagestin
Clinical data
Other namesORG-30659; Exogestin; Letogestin; 11-Methylene-δ-norethisterone; 17α-Ethynyl-11-methylene-19-nor-δ-testosterone
Routes of
administration		By mouth
Identifiers
IUPAC name
  • (1S,2R,10R,11S,14R,15S)-14-ethynyl-14-hydroxy-15-methyl-17-methylidenetetracycloheptadeca-6,12-dien-5-one
CAS Number
PubChem CID
ChemSpider
UNII
KEGG
ChEMBL
CompTox Dashboard (EPA)
Chemical and physical data
FormulaC21H24O2
Molar mass308.421 g·mol
3D model (JSmol)
SMILES
  • CC12CC(=C)C3C(C1C=CC2(C#C)O)CCC4=CC(=O)CCC34
InChI
  • InChI=1S/C21H24O2/c1-4-21(23)10-9-18-17-7-5-14-11-15(22)6-8-16(14)19(17)13(2)12-20(18,21)3/h1,9-11,16-19,23H,2,5-8,12H2,3H3/t16-,17-,18-,19+,20-,21-/m0/s1
  • Key:YJSTYQGZKJHXLN-OLGWUGKESA-N

Tosagestin (INNTooltip International Nonproprietary Name, USANTooltip United States Adopted Name) (developmental code name ORG-30659), also known as 11-methylene-δ-norethisterone or 17α-ethynyl-11-methylene-19-nor-δ-testosterone, is a progestin of the 19-nortestosterone group which was under development by Organon in the United States and Europe as a hormonal contraceptive (in combination with ethinylestradiol) and for the treatment of menopausal symptoms but was never marketed.

See also

References

  1. Negwer M, Scharnow HG (2001). Organic-chemical drugs and their synonyms: (an international survey). Wiley-VCH. p. 2104. ISBN 978-3-527-30247-5.
  2. World Health Organization (2013), The use of stems in the selection of International Nonproprietary Names (INN) for pharmaceutical substances (PDF), p. 95, archived from the original (PDF) on August 8, 2016
  3. "Tosagestin", AdisInsight, Springer Nature Switzerland AG, retrieved 12 July 2016
  4. Verhoeven CH, Krebbers SF, Wagenaars GN, Booy CJ, Groothuis GM, Olinga P, Vos RM (November 1998). "In vitro and in vivo metabolism of the progestagen Org 30659 in several species". Drug Metabolism and Disposition. 26 (11): 1102–1112. PMID 9806953.
  5. de Visser SJ, Uchida N, van Vliet-Daskalopoulou E, Fukazawa I, van Doorn MB, van den Heuvel MW, et al. (September 2003). "Pharmacokinetic differences between Caucasian and Japanese subjects after single and multiple doses of a potential combined oral contraceptive (Org 30659 and EE)". Contraception. 68 (3): 195–202. doi:10.1016/S0010-7824(03)00140-9. PMID 14561540.
  6. Obruca A, Korver T, Huber J, Killick SR, Landgren B, Struijs MJ (July 2001). "Ovarian function during and after treatment with the new progestagen Org 30659". Fertility and Sterility. 76 (1): 108–115. doi:10.1016/S0015-0282(01)01824-6. PMID 11438328.
Progesterone receptor modulators
PRTooltip Progesterone receptor
Agonists
Mixed
(SPRMsTooltip Selective progesterone receptor modulators)
Antagonists
mPRTooltip Membrane progesterone receptor
(PAQRTooltip Progestin and adipoQ receptor)
Agonists
Antagonists
See also
Receptor/signaling modulators
Progestogens and antiprogestogens
Androgen receptor modulators
Estrogen receptor modulators
List of progestogens
Stub icon

This drug article relating to the genito-urinary system is a stub. You can help Misplaced Pages by expanding it.

Stub icon

This article about a steroid is a stub. You can help Misplaced Pages by expanding it.

Categories: