Publication | Open Access

Modulation of PPAR receptor subtype selectivity of the ligands: Aliphatic chain vs aromatic ring as a spacer between pharmacophore and the lipophilic moiety

Lipophilic MoietyBiochemistryFunctional SelectivityMedicineG Protein-coupled ReceptorReceptor (Biochemistry)Mechanism Of ActionPharmacological AgentPharmacotherapyPharmacologyDrug Discovery