Review Article

Structural Development Studies of Subtype-Selective Ligands for Peroxisome Proliferator-Activated Receptors (PPARs) Based on the 3,4-Disubstituted Phenylpropanoic Acid Scaffold as a Versatile Template

Figure 2

Dose-response curves of each enantiomer for PPAR 𝛿 transactivation.
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