Etiprednol

In this article we are going to delve into the topic of Etiprednol. Etiprednol is a topic that has generated great interest in various areas of society, from politics to science. Throughout history, Etiprednol has been the subject of multiple research and debate, leading to greater understanding and knowledge on the topic. In this article we will explore different perspectives and approaches related to Etiprednol, as well as its impact on today's society. From its origin to its future implications, Etiprednol is a highly relevant topic that deserves to be analyzed in depth.

Etiprednol
Clinical data
Other names11β,17α,Dihydroxy-21-oxa-21-ethylpregna-1,4-diene-3,20-dione; Ethyl 11β,17α-dihydroxy-3-oxoandrosta-1,4-diene-17-carboxylate
Drug classCorticosteroid; Glucocorticoid
Identifiers
  • Ethyl (8S,9S,10R,11S,13S,14S,17R)-11,17-Dihydroxy-10,13-dimethyl-3-oxo-7,8,9,11,12,14,15,16-octahydro-6H-cyclopentaphenanthrene-17-carboxylate
CAS Number
PubChem CID
UNII
CompTox Dashboard (EPA)
Chemical and physical data
FormulaC22H30O5
Molar mass374.477 g·mol−1
3D model (JSmol)
  • CCOC(=O)1(CC21(C(32CCC4=CC(=O)C=C34C)O)C)O
  • InChI=1S/C22H30O5/c1-4-27-19(25)22(26)10-8-16-15-6-5-13-11-14(23)7-9-20(13,2)18(15)17(24)12-21(16,22)3/h7,9,11,15-18,24,26H,4-6,8,10,12H2,1-3H3/t15-,16-,17-,18+,20-,21-,22-/m0/s1
  • Key:JTXYEERBIZXLJC-DCJXKKNWSA-N

Etiprednol is a synthetic glucocorticoid corticosteroid.[1][2]

References

  1. ^ Patrick G (20 April 2017). An Introduction to Medicinal Chemistry. Oxford University Press. pp. 772–. ISBN 978-0-19-874969-1.
  2. ^ Lamberth C, Dinges J (17 May 2016). Bioactive Carboxylic Compound Classes: Pharmaceuticals and Agrochemicals. Wiley. pp. 260–. ISBN 978-3-527-69396-2.


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