| Literature DB >> 30996794 |
Letizia Giampietro1, Antonio Laghezza2, Carmen Cerchia3, Rosalba Florio1,4, Lucia Recinella1, Fabio Capone3, Alessandra Ammazzalorso1, Isabella Bruno1, Barbara De Filippis1, Marialuigia Fantacuzzi1, Claudio Ferrante1, Cristina Maccallini1, Paolo Tortorella2, Fabio Verginelli1,4, Luigi Brunetti1, Alessandro Cama1,4, Rosa Amoroso1, Fulvio Loiodice2, Antonio Lavecchia3.
Abstract
The development of PPARα/γ dual or PPARα/γ/δ pan-agonists could represent an efficacious approach for a simultaneous pharmacological intervention on carbohydrate and lipid metabolism. Two series of new phenyldiazenyl fibrate derivatives of GL479, a previously reported PPARα/γ dual agonist, were synthesized and tested. Compound 12a was identified as a PPAR pan-agonist with moderate and balanced activity on the three PPAR isoforms (α, γ, δ). Moreover, docking experiments showed that 12a adopts a different binding mode in PPARγ compared to PPARα or PPARδ, providing a structural basis for further structure-guided design of PPAR pan-agonists. The beneficial effects of 12a were evaluated both in vitro, on the expression of PPAR target key metabolic genes, and ex vivo in two rat tissue inflammatory models. The obtained results allow considering this compound as an interesting lead for the development of a new class of PPAR pan-agonists endowed with an activation profile exploitable for therapy of metabolic syndrome.Entities:
Year: 2019 PMID: 30996794 PMCID: PMC6466826 DOI: 10.1021/acsmedchemlett.8b00574
Source DB: PubMed Journal: ACS Med Chem Lett ISSN: 1948-5875 Impact factor: 4.345