Publication | Open Access

Substituted 4-phenylthiazoles: Development of potent and selective A1, A3 and dual A1/A3 adenosine receptor antagonists

Molecular PharmacologyBiochemistryFunctional SelectivityMedicineMechanism Of ActionPharmacological AgentPharmacotherapySelective A1Heterocycle ChemistryPharmacologyDrug Discovery