Aromatic-Based Design of Highly Active and Noncalcemic Vitamin D Receptor Agonists
datasetposted on 07.05.2018, 00:00 authored by Pranjal Gogoi, Samuel Seoane, Rita Sigüeiro, Thierry Guiberteau, Miguel A. Maestro, Román Pérez-Fernández, Natacha Rochel, Antonio Mouriño
We report the design, synthesis, biological evaluation, and structural analysis of a new class of vitamin D analogues that possess an aromatic m-phenylene D-ring and an alkyl chain replacing the C-ring. A key feature of the synthetic strategy is a stereoselective Pd-catalyzed construction of the triene system in aqueous medium that allows the rapid preparation of small amounts of VDR ligands for biological screening. Analogues with the shorter (2a) and longer (2d, 2e) side chains attached to the triene system have no calcemic activity. Compound 2a binds to VDR with the same order of magnitude than calcipotriol and oxacalcitriol. It also reduces proliferation in normal and tumor cells similarly to the natural hormone 1α,25-dihydroxyvitamin D3, calcipotriol, and oxacalcitriol, suggesting preclinical studies related to hyperproliferative disorders such as psoriasis and cancer.
Read the peer-reviewed publication
VDRstereoselective Pd-catalyzed constructiondihydroxyvitamincalcipotriolAromatic-BasedtumorproliferationhyperproliferativemagnitudestrategyscreeningCompoundevaluationsynthesispsoriasismediumhormoneoxacalcitriolNoncalcemic Vitamin D Receptor Agonistsligandalkylanalysispreparationphenylenetriene systemvitamin D analoguesAnaloguedisorder