[1] T FURUKAWA. Selectivities of dihydropyridine derivatives in blocking Ca(2+) channel subtypes expressed in Xenopus oocytes.[J]. Journal of Pharmacology and Experimental Therapeutics, 1999, 291 2: 464-473.
[2] J D JOHNSON D A F. Calcium and calmodulin antagonists binding to calmodulin and relaxation of coronary segments.[J]. Journal of Pharmacology and Experimental Therapeutics, 1983, 226 2: 330-334.
[3] EDWARD PEREZ-REYES I V Amy L Van Deusen. Molecular pharmacology of human Cav3.2 T-type Ca2+ channels: block by antihypertensives, antiarrhythmics, and their analogs.[J]. Journal of Pharmacology and Experimental Therapeutics, 2009, 328 1: 621-627. DOI:
10.1124/jpet.108.145672[4] LJUNG B. Vascular selectivity of felodipine: experimental pharmacology.[J]. Journal of Cardiovascular Pharmacology, 1990, 15 Suppl 4: S11-6. DOI:
10.1097/00005344-199015004-00003[5] G R BOLT P R S. Acute systemic and regional hemodynamic effects of felodipine, a new calcium antagonist, in conscious renal hypertensive rabbits.[J]. Journal of Cardiovascular Pharmacology, 1984, 6 4: 707-712. DOI:
10.1097/00005344-198407000-00025