Severina I S, Ryaposova I K, Volodarsky L B, Mozhuchin D C, Granik V G, Grigoryev D A, Grigoryev N B
Institute of Biomedical Chemistry, Russian Academy of Medical Sciences, Moscow.
Biochem Mol Biol Int. 1993 Jun;30(2):357-66.
Derivatives of diazetidine-di-N-oxides have been found capable of the nonenzymatic generation of nitric oxide by the principally new mechanism of the nitric oxide splitting at physiological pH values. The effect of the synthesized compounds on human platelet soluble guanylate cyclase activity as well as their spasmolytic and hypotensive action were studied. Four of 7 derivatives studied exhibited a distinct correlation between the ability of being decomposed with the nitric oxide formation, activation of soluble guanylate cyclase, and spasmolytic and antihypertensive activities. Among them, 3-brom, 4-methyl-3,4-tetramethylene-diazetidine-di-N-oxide has proved to be most effective, its spasmolytic effect being commensurable with glyceryl trinittrate activity. The revealed correlation allows us to regard 1,2-diazetidine-1,2-di-N-oxide derivatives as vasodilatory agents of a new class.
已发现二氮杂环丁烷二-N-氧化物的衍生物能够通过在生理pH值下一氧化氮分解的主要新机制非酶促生成一氧化氮。研究了合成化合物对人血小板可溶性鸟苷酸环化酶活性及其解痉和降压作用。所研究的7种衍生物中有4种在分解生成一氧化氮的能力、可溶性鸟苷酸环化酶的激活以及解痉和抗高血压活性之间表现出明显的相关性。其中,3-溴-4-甲基-3,4-四亚甲基-二氮杂环丁烷二-N-氧化物已被证明是最有效的,其解痉作用与三硝酸甘油酯活性相当。所揭示的相关性使我们能够将1,2-二氮杂环丁烷-1,2-二-N-氧化物衍生物视为一类新型的血管扩张剂。