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Ticabesone

From Wikipedia, the free encyclopedia
Chemical compound
Pharmaceutical compound
Ticabesone
Clinical data
Other names6α,9α-Difluoro-11β,17α-dihydroxy-16α-methyl-21-methyl-21-thiapregna-1,4-dien-3,20-dione; S-Methyl 6α,9α-difluoro-11β,17α-dihydroxy-16α-methyl-3-oxoandrosta-1,4-diene-17β-carbothioate
Drug classCorticosteroid;Glucocorticoid
Identifiers
  • S-Methyl (6S,8S,9R,10S,11S,13S,14S,16R,17R)-6,9-Difluoro-11,17-dihydroxy-10,13,16-trimethyl-3-oxo-6,7,8,11,12,14,15,16-octahydrocyclopenta[a]phenanthrene-17-carbothioate
CAS Number
PubChemCID
UNII
CompTox Dashboard(EPA)
Chemical and physical data
FormulaC22H28F2O4S
Molar mass426.52 g·mol−1
3D model (JSmol)
  • C[C@@H]1C[C@H]2[C@@H]3C[C@@H](C4=CC(=O)C=C[C@@]4([C@]3([C@H](C[C@@]2([C@]1(C(=O)SC)O)C)O)F)C)F
  • InChI=1S/C22H28F2O4S/c1-11-7-13-14-9-16(23)15-8-12(25)5-6-19(15,2)21(14,24)17(26)10-20(13,3)22(11,28)18(27)29-4/h5-6,8,11,13-14,16-17,26,28H,7,9-10H2,1-4H3/t11-,13+,14+,16+,17+,19+,20+,21+,22+/m1/s1
  • Key:TYVHQHCXWZVELU-GQKYHHCASA-N

Ticabesone is asyntheticglucocorticoidcorticosteroid which was never marketed.[1][2][3]

References

[edit]
  1. ^Lednicer D (20 June 2011).Steroid Chemistry at a Glance. John Wiley & Sons. pp. 5–.ISBN 978-1-119-95729-4.
  2. ^Lednicer D (4 March 2009).Strategies for Organic Drug Synthesis and Design. John Wiley & Sons. pp. 183–.ISBN 978-0-470-39959-0.
  3. ^Challener CA (1 December 2001).Chiral Drugs. Wiley. p. 435.ISBN 978-0-566-08411-9.


GRTooltip Glucocorticoid receptor
Agonists
Mixed
(SEGRMsTooltip Selective glucocorticoid receptor agonists)
Antagonists
Others


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