Parallel Chemistry Approach to Identify Novel Nuclear Receptor Ligands Based on the GW0742 Scaffold.

ABSTRACT: We describe the parallel synthesis of novel analogs of GW0742, a peroxisome proliferator-activated receptor ? (PPAR?) agonist. For that purpose, modified reaction conditions were applied, such as a solid-phase palladium-catalyzed Suzuki coupling. In addition, tetrazole-based compounds were generated as a bioisostere for carboxylic acid-containing ligand GW0742. The new compounds were investigated for their ability to activate PPAR? mediated transcription and their cross-reactivity with the vitamin D receptor (VDR), another member of the nuclear receptor superfamily. We identified many potent PPAR? agonists that were less toxic than GW0742, where ?65 of the compounds synthesized exhibited partial PPAR? activity (23-98%) with EC50 values ranging from 0.007-18.2 ?M. Some ligands, such as compound 32, were more potent inhibitors of VDR-mediated transcription with significantly reduced PPAR? activity than GW0742, however, none of the ligands were completely selective for VDR inhibition over PPAR? activation of transcription.

SUBMITTER: Teske KA 

PROVIDER: S-EPMC5643073 | biostudies-literature | 2017 Oct

REPOSITORIES: biostudies-literature