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首页> 外文期刊>Japanese Journal of Pharmacology >EFFECT OF 8-SUBSTITUTED CYCLIC AMP DERIVATIVES ON SOLUBLE GUANYLATE CYCLASE ACTIVITY FROM HUMAN PLATELETS
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EFFECT OF 8-SUBSTITUTED CYCLIC AMP DERIVATIVES ON SOLUBLE GUANYLATE CYCLASE ACTIVITY FROM HUMAN PLATELETS

机译:8取代的环安培衍生物对人血小板中可溶性瓜氨酸盐环化酶活性的影响

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References(15) Inhibitory effect of 8-alkyl cyclic AMP derivatives on the soluble guanylate cyclase activity from human platelets was investigated. Cyclic AMP derivatives with alkyl chains of 6 or less carbons at 8-position of the purine base were not inhibitory, but the derivatives with alkyl chains of 7 or more carbons produced significant inhibition of the soluble guanylate cyclase activity. The extent of inhibitory effect increased when a longer alkyl chain was introduced at the 8-position of cyclic AMP. In contrast, 8-alkyl adenosine derivatives did not inhibit the cyclase activity. These results suggest that the platelet guanylate cyclase has an affinity for cyclic AMP derivatives with hydrophobic property as well as for several guanine nucleotides such as GTP or cyclic GMP.
机译:参考文献(15)研究了8烷基环状AMP衍生物对人血小板中可溶性鸟苷酸环化酶活性的抑制作用。在嘌呤碱基的8位碳数为6或更少的烷基链的环AMP衍生物没有抑制作用,但碳数为7或更多的烷基链的衍生物对可溶性鸟苷酸环化酶活性产生了明显的抑制作用。当在环状AMP的8位引入更长的烷基链时,抑制作用的程度增加。相反,8-烷基腺苷衍生物不抑制环化酶活性。这些结果表明血小板鸟苷酸环化酶对具有疏水性质的环状AMP衍生物以及几种鸟嘌呤核苷酸如GTP或环状GMP具有亲和力。

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