Determination of ionization constants of N-imidazole derivatives, aromatase inhibitors, using capillary electrophoresis and influence of substituents on pKa shifts

被引:30
作者
Foulon, C
Danel, C
Vaccher, C
Yous, S
Bonte, JP
Goossens, JF
机构
[1] Univ Lille 2, Fac Sci Pharmaceut & Biol, Chim Analyt Lab, F-59006 Lille, France
[2] Univ Lille 2, Fac Sci Pharmaceut & Biol, Chim Therapeut Lab, F-59006 Lille, France
关键词
ionization constants; dissociation constants; imidazoles; enzyme inhibitors; benzoxazolinones; benzothiazolmones;
D O I
10.1016/j.chroma.2004.02.053
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Capillary electrophoresis (CE) was used as a method to determine the acidity constants of eight aromatase inhibitors. This method was validated by comparison of results obtained with a traditional method, UV spectroscopy, and additionally with computational calculations. We confirmed here, with our series of compounds, that capillary electrophoresis is an attractive method for pK(a) measurements which is based on migration time or mobilities of the ionic species over a range of pH values. The precision of pK(a) measurements of N-imidazole derivatives is useful to observe pK(a) shifts induced by chemical modifications introduced on adjacent aromatic rings such as heterocycle (benzoxa- or benzothiazolinone) or substituted benzyle. The knowledge of these pK(a) values is a great interest to predict migration of solutes and qualitative interactions with ionized cyclodextrines as chiral selectors in further enantioseparative CE studies. (C) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:131 / 136
页数:6
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