Hantzsch 1,4-dihydropyridines containing a diazen-1-ium-1,2-diolate nitric oxide donor moiety to study calcium channel antagonist structure–activity relationships and nitric oxide release

Abstract

A group of racemic 3-isopropyl 5-[(2-piperazin-1-yl)ethyl] 1,4-dihydro-2,6-dimethyl-4-(pyridyl)-3,5-pyridinedicarboxylates ( 12a– c), 3-isopropyl 5-{2-[4-nitrosopiperazinyl]ethyl} 1,4-dihydro-2,6-dimethyl-4-(pyridyl)-3,5-pyridinedicarboxylates ( 14a– c) and 3-isopropyl 5-{2-[( O 2-acetoxymethyldiazen-1-ium-1,2-diolate)( N, N-dialkylamino or 4-piperazin-1-yl)]ethyl} 1,4-dihydro-2,6-dimethyl-4-(pyridyl)-3,5-pyridinedicarboxylates ( 22– 30) were prepared using modified Hantzsch reactions. This group of compounds ( 12a– c, 14a– c, and 22– 30) exhibited less potent calcium channel antagonist activity (IC 50 = 0.11 to 3.35 μM range) than the reference drug nifedipine (IC 50 = 0.01 μM). The point of attachment of the isomeric C-4 substituent was a determinant of calcium channel antagonist activity providing the potency profile 2-pyridyl ⩾ 3-pyridyl ⩾ 4-pyridyl. The N-nitrosopiperazinyl compounds ( 14a– c) did not release nitric oxide. The prodrugs 22– 30 that have a C-5 2-[( O 2-acetoxymethyldiazen-1-ium-1,2-diolate)( N, N-dialkylamino or 4-piperazin-1-yl)]ethyl ester substituent, upon incubation with guinea pig serum, undergo consecutive cleavage of the O 2-acetoxymethyl moiety to give a nitric oxide donor diazenium-1-ium-1,2-diolate species that subsequently releases nitric oxide. The extent of nitric oxide released from the diazen-1-ium-1,2-diolate group is dependent upon the nature of the amino functionality attached directly to the diazen-1-ium N-1 position where the nitric oxide release profile is 1,4-piperazinyl > N-Et > N-( n-Bu) ≫ N-Me upon exposure to guinea pig serum esterase(s). The results from this study suggest this class of hybrid calcium channel antagonist/nitric oxide donor prodrugs should release the vasodilator nitric oxide in vivo, preferentially in the vascular endothelium, to enhance the smooth muscle calcium channel antagonist effect to produce a combined synergistic antihypertensive effect.