Chiral resolution of the enantiomers of new selective CB2 receptor agonists by liquid chromatography on amylose stationary phases

Journal of Pharmaceutical and Biomedical Analysis

Volumn 46, Issue 5, 2008, Pages 848-853

  Stern, E ^a   Goossens, L ^a   Vaccher, C ^b   Bonte, J P ^b   Depreux, P ^a   Henichart, J P ^a   Goossens, J F ^b  

^a Faculté des Sciences Pharmaceutiques et Biologiques Université de Lille   (France)

^b UNIV LILLE   (France)

Author keywords

4 Quinolone; CB2 receptor agonists; Chiral stationary phases; Enantiomers separation; Validation method

Indexed keywords

4 OXO 1,4 DIHYDROQUINOLINE 3 CARBOXAMIDE DERIVATIVE; AMYLOSE; CANNABINOID 2 RECEPTOR; CANNABINOID 2 RECEPTOR STIMULATING AGENT; CANNABINOID RECEPTOR AGONIST; UNCLASSIFIED DRUG;

ARTICLE; CHIRAL CHROMATOGRAPHY; DRUG SCREENING; DRUG SYNTHESIS; ENANTIOMER; ENANTIOSELECTIVITY; HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; LIQUID CHROMATOGRAPHY; PRIORITY JOURNAL; RACEMIC MIXTURE; ULTRAVIOLET RADIATION;

AMYLOSE; CARBAMATES; CHROMATOGRAPHY, HIGH PRESSURE LIQUID; MOLECULAR STRUCTURE; PHENYLCARBAMATES; QUINOLINES; RECEPTOR, CANNABINOID, CB2; REPRODUCIBILITY OF RESULTS; SOLVENTS; SPECTROPHOTOMETRY, ULTRAVIOLET; STEREOISOMERISM; TECHNOLOGY, PHARMACEUTICAL; TEMPERATURE;

EID: 40849100075     PISSN: 07317085     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.jpba.2007.01.044     Document Type: Article

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