Enantioselective binding to the human organic cation transporter‐1 (hOCT1) determined using an immobilized hOCT1 liquid chromatographic stationary phase

Publisher Website
Google Scholar
Abstract
A liquid chromatography stationary phase containing immobilized membranes obtained from a cell line that expresses the human organic cation transporter (hOCT1–IAM) has been used to study the binding of the enantiomers of propranolol, atenolol, pseudoephedrine, and α-methylbenzylamine to the immobilized hOCT1. Frontal displacement chromatography was used to determine the binding affinities (Kd values), and the data demonstrate that there was an enantioselective difference in the Kd values of the enantiomers of propranolol, atenolol, and pseudoephedrine, while α-methylbenzylamine did not significantly bind to the transporter. Competitive inhibition studies with the cell line used to create the chromatographic column demonstrated that, for the enantiomers of propranolol, the ratio of the chromatographically determined Kd values [Kd (+)-(R)-propranolol/Kd (−)-(S)-propranolol = 2.98] reflected an enantioselective difference in the functional activity of the two enantiomers [IC50 (+)-(R)-propranolol/IC50 (−)-(S)-propranolol = 2.75]. The chromatographically determined Kd values were used to construct an initial pharmacophore which contains a hydrogen bond donating site that appears to be responsible for the observed enantioselectivity. Published 2005 Wiley-Liss, Inc.† Chirality 17:501–506, 2005.

This publication has 11 references indexed in Scilit: