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川芎嗪的抗血小板构效关系。

Antiplatelet structure-activity relationship of tetramethylpyrazine.

作者信息

Liu S Y, Sylvester D M

机构信息

Pharmacology/Toxicology Graduate Program, Washington State University, Pullman 99164-6510.

出版信息

Life Sci. 1994;55(17):1317-26. doi: 10.1016/0024-3205(94)00764-0.

Abstract

Tetramethylpyrazine (TMPZ) is an active component of certain plants previously found to have inhibitory effects on platelet function using both in vivo and in vitro assays(1). In this study, we examined the antiplatelet activity of structural analogues of TMPZ in order to assess structural requirements for activity. Functional requirements included nitrogen substitutions on the aromatic ring; substitutions could be either heterocyclic or ring substituted in the meta position. Enhanced antiplatelet activity was associated with increasing the number of alkyl groups on the pyrazine ring as well as increasing the length of unbranched alkyl side chains. Increased inhibition of platelet aggregation correlated with increased lipophilicity of the compounds tested. In addition, several compounds were identified which deserve further pharmacological investigation.

摘要

川芎嗪(TMPZ)是某些植物的活性成分,此前通过体内和体外试验发现其对血小板功能具有抑制作用(1)。在本研究中,我们检测了TMPZ结构类似物的抗血小板活性,以评估活性的结构要求。功能要求包括芳环上的氮取代;取代基可以是杂环或间位环取代。抗血小板活性增强与吡嗪环上烷基数量的增加以及直链烷基侧链长度的增加有关。所测试化合物的亲脂性增加与血小板聚集抑制作用增强相关。此外,还鉴定出几种值得进一步进行药理学研究的化合物。

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