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The structurally novel Ca2+ channel blocker Ro 40-5967, which binds to the [3H] desmethoxyverapamil receptor, is devoid of the negative inotropic effects of verapamil in normal and failing rat hearts

Molecular PharmacologyCardiomyopathyHeart FailureMolecular PhysiologyCardiac MuscleBiochemistryMedicinePhysiologyFailing Rat HeartsCardiovascular PharmacologyPharmacotherapyCardiovascular ToxicityPharmacologyCardiologyNegative Inotropic EffectsOxidative Stress