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喹哪啶衍生物:制备方法与生物活性

Quinaldine derivatives: preparation and biological activity.

作者信息

Jampilek Josef, Dolezal Martin, Kunes Jiri, Buchta Vladimir, Silva Luis, Kralova Katarina

机构信息

Zentiva a.s., U kabelovny 130, 102 37 Prague 10, Czech Republic.

出版信息

Med Chem. 2005 Nov;1(6):591-9. doi: 10.2174/157340605774598108.

Abstract

The series of quinaldine derivatives were prepared, some of them by means of novel synthetic methods. The synthetic approach, analytical and spectroscopic data of all newly synthesized compounds are presented. The prepared compounds were tested for their in vitro antifungal activity as well as for their photosynthesis-inhibiting activity (the inhibition of photosynthetic electron transport in spinach chloroplasts (Spinacia oleracea L.) and the reduction of chlorophyll content in Chlorella vulgaris Beij.). Structure-activity relationships among the chemical structure, the physical properties and the biological activities of the evaluated compounds are discussed in the article.

摘要

制备了一系列喹哪啶衍生物,其中一些是通过新颖的合成方法制备的。介绍了所有新合成化合物的合成方法、分析和光谱数据。对所制备的化合物进行了体外抗真菌活性以及光合作用抑制活性测试(抑制菠菜叶绿体(Spinacia oleracea L.)中的光合电子传递以及普通小球藻(Chlorella vulgaris Beij.)中叶绿素含量的降低)。文章讨论了所评估化合物的化学结构、物理性质和生物活性之间的构效关系。

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