ABSTRACT
Nicorandil (N-(2-hydroxyethyl)nicotinamide nitrate) is an antianginal drug, which activates guanylyl cyclase and opens the ATP-dependent K(+) channels, actions that have been suggested to mediate its vasodilator activity. We synthesized nicorandil and its two isomers, which vary in the positions of the side chain containing the nitric oxide (NO) donor, and also their corresponding denitrated metabolites. The activities of these compounds were evaluated in an experimental model of pain in mice. Pharmacokinetic parameters of nicorandil and its isomers, as well as the plasma concentrations of the corresponding denitrated metabolites and also nicotinamide and nitrite were determined. Nicorandil exhibited the highest antinociceptive activity, while the ortho-isomer was the least active. Nicorandil and para-nicorandil, which induced higher plasma concentrations of nitrite, exhibited higher antinociceptive activity, which suggests that the release of NO may mediate this activity.
Subject(s)
Analgesics/chemical synthesis , Nicorandil/chemistry , Analgesics/pharmacokinetics , Analgesics/therapeutic use , Animals , Disease Models, Animal , Female , Half-Life , Isomerism , Mice , Nicorandil/pharmacokinetics , Nicorandil/therapeutic use , Pain/drug therapyABSTRACT
In the title mol-ecule, C(8)H(9)N(3)O(4), the amide group is involved in the formation of an intra-molecular N-Hâ¯N hydrogen bond. In the crystal, mol-ecules related by translation along the a axis are linked into chains via weak inter-molecular C-Hâ¯O inter-actions.
