Binding site for basic drugs on α1‐acid glycoprotein as revealed by chemometric analysis of biochromatographic data
- 1 September 1995
- journal article
- research article
- Published by Wiley in Biomedical Chromatography
- Vol. 9 (5) , 211-215
- https://doi.org/10.1002/bmc.1130090504
Abstract
Interactions between α1-acid glycoprotein (AGP) and 52 basic drugs were quantified by means of highperformance liquid chromatography (HPLC). The HPLC retention parameters were related quantitatively to the hydrophobicity and molecular modelling parameters, giving rise to the prediction of relative drug-AGP binding from the chemical structure of a drug. A structural model of one binding site on AGP, common for various classes of drugs, was defined which accounted for the observed and reported differences in binding to AGP. A combination of biochromatography and chemometrics has been presented as a promising new approach in biochemical/pharmacological studies.Keywords
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