Description
A dihydropyridine L-type calcium channel blocker; binds to rat brain and heart homogenates (Kis = 0.24-0.3 and 0.22 nM, respectively, in radioligand binding assays) and inhibits potassium-induced contraction of isolated rat aorta (IC50 = 1.3 nM); reduces DBP in normotensive and spontaneously hypertensive rats (ED25s = 16.3 and 15.5 µg/kg, respectively)
Formal name: 3,5-pyridinedicarboxylic acid, 1,4-dihydro-2,6-dimethyl-4-(3-nitrophenyl)-3-[2-[(3,3-diphenylpropyl)methylamino]-1,1-dimethylethyl] 5-methyl ester, monohydrochloride
Synonyms:
Molecular weight: 648.2
CAS: 132866-11-6
Purity: ≥98%
Formulation: A solid