Literature DB >> 1810960

Direct enantiomeric separation of terfenadine and its major acid metabolite by high-performance liquid chromatography, and the lack of stereoselective terfenadine enantiomer biotransformation in man.

K Y Chan1, R C George, T M Chen, R A Okerholm.   

Abstract

Direct enantiomeric separation of terfenadine and its major acid metabolite was achieved by using two different chiral stationary phase columns with two different mobile phase systems. Further, the enantiomeric composition of the human urinary acid metabolite has been determined, indicating a non-stereoselective biotransformation in man.

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Year:  1991        PMID: 1810960     DOI: 10.1016/0378-4347(91)80458-o

Source DB:  PubMed          Journal:  J Chromatogr


  2 in total

1.  Mechanism of block of a human cardiac potassium channel by terfenadine racemate and enantiomers.

Authors:  T Yang; C Prakash; D M Roden; D J Snyders
Journal:  Br J Pharmacol       Date:  1995-05       Impact factor: 8.739

Review 2.  Terfenadine: a mixture of equipotent antihistamine enantiomers without a clear 'isomeric ballast'.

Authors:  M Q Zhang; H Timmerman
Journal:  Pharm World Sci       Date:  1993-10-15
  2 in total

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