Sunil Gaikwad, Carmen M González, Daniel Vilariño, Gonzalo Lasanta, Carmen Villaverde, Antonio Mouriño, Lieve Verlinden, Annemieke Verstuyf, Carole Peluso-Iltis, Natacha Rochel, Klaudia Berkowska, Ewa Marcinkowska
Journal: Bioorganic chemistry 2021;111():104878
PMID: 33853023
The hypercalcemic effects of the hormone 1α,25-dihydroxyvitamin D (calcitriol) and most of known vitamin D metabolites and analogs call for the development of non secosteroidal vitamin D receptor (VDR) ligands as new selective and noncalcemic agonists for treatment of hyperproliferative diseases. We report on the in silico design and stereoselective synthesis of six lithocholic acid derivatives as well as on the calcemic activity of a potent LCA derivative and its crystallographic structure in complex with zVDR LBD. The low calcemic activity of this compound in comparison with the native hormone makes it of potential therapeutic value. Structure-function relationships provide the basis for the development of even more potent and selective lithocholic acid-based VDR ligands.
Copyright © 2021 Elsevier Inc. All rights reserved.
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