Structural studies of loteprednol etabonate and other analogs of prednisolone using NMR techniques

  • Rachwal S
  • Pop E
  • Brewster M
  • 3


    Mendeley users who have this article in their library.
  • 12


    Citations of this article.


Severed structural analogy of prednisolone, prepared by esterification of the carboxylic and/or the C(17)-hydroxy group of 11β,17α-dihydroxy-3- oxo-androsta-1,4-diene-17β-carboxylic acid, were invextigated by NMR. Step- by-step analysis of the1H and13C NMR spectra of these steroids, including proton-proton selective decoupling, nuclear Overhuaser effect difference spectra, attached proton test, proton-carbon correlation (HETCOR), proton-proton correlation (COSY), and long-range proton-carbon decoupling (INAPT) techniques, led to unequivocat assignments of all their proton and carbon resonances. The stereochemical structure of loteprednol etabonate (chloromethyl 17α-ethoxycarbonyloxy-11β-hydroxy,-3-oxoandrosta-1,4 diene- 17β-carboxylate, 1), a soft corticosteroid antiinflammatory drug, was proved to be analogous to prednisolone.

Author-supplied keywords

  • 11β-hydroxy-3-oxoandrosta-1,4-diene-17β-carboxylate
  • 13C NMR
  • 1H NMR
  • prednisolone analog

Get free article suggestions today

Mendeley saves you time finding and organizing research

Sign up here
Already have an account ?Sign in

Find this document


  • Stanislaw Rachwal

  • Emil Pop

  • Marcus E. Brewster

Cite this document

Choose a citation style from the tabs below

Save time finding and organizing research with Mendeley

Sign up for free