Basséne Carine Ekambomé, Suzenet Franck, Hennuyer Nathalie, Staels Bart, Caignard Daniel-Henri, Dacquet Catherine, Renard Pierre, Guillaumet Gérald
Institut de Chimie Organique et Analytique (ICOA), UMR-CNRS 6005, FR CNRS 2708, Université d'Orléans, France.
Bioorg Med Chem Lett. 2006 Sep 1;16(17):4528-32. doi: 10.1016/j.bmcl.2006.06.028. Epub 2006 Jun 23.
In order to define new PPARbeta/delta ligands, SAR study on the selective PPARbeta/delta activator L-165,041 led to the identification of one key functional group for selective PPARbeta/delta activation. Furthermore, taking advantage of SAR studies done elsewhere on the most selective PPARbeta/delta ligand GW501516, the conception of new ligands showing good affinity for PPARbeta/delta is reported. Finally, synthesis and biological evaluation of pyridine analogues have shown the benefical effect of the pyridine ring on the PPARbeta/delta subtype selectivity.
为了确定新的PPARβ/δ配体,对选择性PPARβ/δ激活剂L-165,041进行的构效关系(SAR)研究导致确定了一个用于选择性PPARβ/δ激活的关键官能团。此外,利用在其他地方对最具选择性的PPARβ/δ配体GW501516所做的SAR研究,报道了对PPARβ/δ具有良好亲和力的新配体的构想。最后,吡啶类似物的合成和生物学评价表明吡啶环对PPARβ/δ亚型选择性具有有益作用。