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Novel potent and selective Ca2+ release-activated Ca2+ (CRAC) channel inhibitors. Part 3: Synthesis and CRAC channel inhibitory activity of 4′-[(trifluoromethyl)pyrazol-1-yl]carboxanilides

Channel InhibitorsMolecular PharmacologyMedicinal ChemistryBiochemistryMedicineNatural SciencesNovel PotentPharmacologyPharmaceutical ChemistryInhibitory ActivityDrug Discovery