GW0742 CS-5560

GW0742 attenuates hepatic endoplasmic gw0742 GW0742 is a potent and highly selective PPARβδ agonist, with IC50 of 1 nM, with 1000-fold selectivity over hPPARα and hPPARγ gw0742 GW0742 docking conformation compared to the GW0742 of the crystal structure 3D detail of the amino acids forming polar bindings with GW0742

gw0742 Avis client GW0742 is a potent PPARβ and PPARδ agonist, with an IC50 of 1 nM for human PPARδ, and EC50s of 1 nM, μM and 2 μM for human PPARδ, PPARα, and