Novel selective PPARδ agonists: Optimization of activity by modification of alkynylallylic moiety

Novel selective PPARδ agonists: Optimization of activity by modification of alkynylallylic moiety Novel selective small molecule agonists for peroxisome proliferator-activated receptor δ (PPARδ)—synthesis and biological activity Design, synthesis, and biological evaluation of a series of alkoxy-3-indolylacetic acids as peroxisome proliferator-activated receptor γ/δ agonists Identification and Synthesis of a Novel Selective Partial PPARδ Agonist with Full Efficacy on Lipid Metabolism In Vitro and In Vivo Selective, potent PPARγ agonists with cyclopentenone core structure Indanylacetic Acid Derivatives Carrying 4-Thiazolyl-phenoxy Tail Groups, a New Class of Potent PPAR α/γ/δ Pan Agonists:  Synthesis, Structure−Activity Relationship, and In Vivo Efficacy Design and synthesis of novel Y-shaped barbituric acid derivatives as PPARγ activators Discovery and structure-based design of a new series of potent and selective PPARδ agonists utilizing a virtual screening method Design of potent PPARα agonists 2-Alkoxydihydrocinnamates as PPAR agonists. Activity modulation by the incorporation of phenoxy substituents