| Literature DB >> 33620196 |
Markus Hartmann1, Sofia-Iris Bibli2, Daniel Tews3, Xiaomin Ni1, Theresa Kircher1, Jan S Kramer1, Whitney Kilu1, Jan Heering4, Victor Hernandez-Olmos4, Lilia Weizel1, Gerhard K E Scriba5, Sulaiman Krait5, Stefan Knapp1,6, Apirat Chaikuad1,6, Daniel Merk1, Ingrid Fleming2, Pamela Fischer-Posovszky3, Ewgenij Proschak1,4.
Abstract
The metabolic syndrome (MetS) is a constellation of cardiovascular and metabolic symptoms involving insulin resistance, steatohepatitis, obesity, hypertension, and heart disease, and patients suffering from MetS often require polypharmaceutical treatment. PPARγ agonists are highly effective oral antidiabetics with great potential in MetS, which promote adipocyte browning and insulin sensitization. However, the application of PPARγ agonists in clinics is restricted by potential cardiovascular adverse events. We have previously demonstrated that the racemic dual sEH/PPARγ modulator RB394 (3) simultaneously improves all risk factors of MetS in vivo. In this study, we identify and characterize the eutomer of 3. We provide structural rationale for molecular recognition of the eutomer. Furthermore, we could show that the dual sEH/PPARγ modulator is able to promote adipocyte browning and simultaneously exhibits cardioprotective activity which underlines its exciting potential in treatment of MetS.Entities:
Year: 2021 PMID: 33620196 DOI: 10.1021/acs.jmedchem.0c02063
Source DB: PubMed Journal: J Med Chem ISSN: 0022-2623 Impact factor: 7.446