Literature DB >> 8335715

Direct determination of the enantiomers of halofantrine and its pharmacologically active metabolite N-desbutylhalofantrine by high-performance liquid chromatography.

H Terefe1, G Blaschke.   

Abstract

The enantiomers of halofantrine and its main metabolite, N-desbutylhalofantrine, were separated on two different polysaccharide-based chiral stationary phases. The steroselective biotransformation of halofantrine was determined using rat liver homogenates. (-)-Halofantrine is metabolized preferentially.

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Year:  1993        PMID: 8335715     DOI: 10.1016/0378-4347(93)80352-5

Source DB:  PubMed          Journal:  J Chromatogr


  2 in total

1.  X-ray crystal structure of the antimalarial agent (-)-halofantrine hydrochloride supports stereospecificity for cardiotoxicity.

Authors:  J M Karle
Journal:  Antimicrob Agents Chemother       Date:  1997-04       Impact factor: 5.191

Review 2.  Clinical pharmacokinetics of halofantrine.

Authors:  J Karbwang; K Na Bangchang
Journal:  Clin Pharmacokinet       Date:  1994-08       Impact factor: 6.447

  2 in total

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