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Cyanomidines. II. Synthesis and Pharmacological Activity of N-Arylalkyl-N'-cyano-3-pyridinecarboxamidines.

1994; Pharmaceutical Society of Japan; Volume: 42; Issue: 12 Linguagem: Inglês

10.1248/cpb.42.2483

1347-5223

Tatsuo Nakajima, Satoru Nakajima, Takeshi Izawa, Tomoko Kashiwabara, Y. MUNEZUKA,

Synthesis and Biological Evaluation

A new series of cyanoamidines, N-arylalkyl-N'-cyano-3-pyridinecarboxamidines was synthesized and evaluated for inhibitory effects on 40 mM KCl-induced contraction and norepinephrine (NE)-induced contraction of rat aorta strips. The N-phenethyl cyanoamidine 4c showed potent vasodilatory action. Further in vitro screening program using 4c as a lead compound resulted in the discovery of highly potent N-[2-(2-chlorophenyl)ethyl]-N'-cyano-3-pyridinecarboxamidine (5j). Compound 5j induced the greatest increase in 86Rb+ efflux among cyanoamidine series. Subsequent modification of the pyridine ring of 5j was performed with evaluation for intravenous and oral antihypertensive activities. Introduction of an amino group at the 5-position of the pyridine ring furnished the new potassium channel opener, 5-amino-N-[2-(2-chlorophenyl)ethyl]-N'-cyano-3-pyridinecarboxamidine+ ++ (9e; KRN4884), which showed highly potent antihypertensive activity and a long duration of antihypertensive action after oral administration. KRN4884 is under further development as an antihypertensive agent.