Literature DB >> 6328130

Resolution of the stereoisomers of baclofen by high performance liquid chromatography.

R P Weatherby, R D Allan, G A Johnston.   

Abstract

The GABA analogue baclofen [3-(p-chlorophenyl)-4-aminobutanoic acid] has stereospecific actions on the peripheral and central nervous systems. This paper describes the resolution of tritium-labelled baclofen by high performance liquid chromatography on a reverse-phase C18 column using a chiral mobile phase. The method, which may have general application to certain other GABA analogues, affords optically pure (+)- and (-)-baclofen labelled with tritium to high specific activity suitable for ligand binding and other neurochemical studies.

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Year:  1984        PMID: 6328130     DOI: 10.1016/0165-0270(84)90076-1

Source DB:  PubMed          Journal:  J Neurosci Methods        ISSN: 0165-0270            Impact factor:   2.390


  4 in total

Review 1.  Spasticity and drug therapy.

Authors:  E W Wuis
Journal:  Pharm Weekbl Sci       Date:  1987-10-16

2.  Resolution of Enantiomers of (RS)-Baclofen by Ligand-Exchange Thin-Layer Chromatography.

Authors:  Manisha Singh; Poonam Malik; Ravi Bhushan
Journal:  J Chromatogr Sci       Date:  2016-02-18       Impact factor: 1.618

3.  Enantiospecific high-performance liquid chromatographic (HPLC) determination of baclofen and its fluoro analogue in biological material.

Authors:  H Spahn; D Krauss; E Mutschler
Journal:  Pharm Res       Date:  1988-02       Impact factor: 4.200

Review 4.  GABAB Receptor Chemistry and Pharmacology: Agonists, Antagonists, and Allosteric Modulators.

Authors:  A Nieto; T Bailey; K Kaczanowska; P McDonald
Journal:  Curr Top Behav Neurosci       Date:  2022
  4 in total

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