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首页> 外文期刊>Future medicinal chemistry >Inhibitors of fatty acid synthesis in prokaryotes and eukaryotes as anti-infective, anticancer and anti-obesity drugs
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Inhibitors of fatty acid synthesis in prokaryotes and eukaryotes as anti-infective, anticancer and anti-obesity drugs

机译:原核生物和真核生物中脂肪酸合成的抑制剂,作为抗感染,抗癌和抗肥胖药

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摘要

There is a large range of diseases, such diabetes and cancer, which are connected to abnormal fatty acid metabolism in human cells. Therefore, inhibitors of human fatty acid synthase have great potential to manage or treat these diseases. In prokaryotes, fatty acid synthesis is important for signaling, as well as providing starting materials for the synthesis of phospholipids, which are required for the formation of the cell membrane. Recently, there has been renewed interest in the development of new molecules that target bacterial fatty acid synthases for the treatment of bacterial diseases. In this review, we look at the differences and similarities between fatty acid synthesis in humans and bacteria and highlight various small molecules that have been shown to inhibit either the mammalian or bacterial fatty acid synthase or both.
机译:有许多疾病,例如糖尿病和癌症,与人类细胞中异常的脂肪酸代谢有关。因此,人脂肪酸合酶的抑制剂具有控制或治疗这些疾病的巨大潜力。在原核生物中,脂肪酸的合成对于信号传递非常重要,也为合成细胞膜所需的磷脂提供了起始原料。最近,人们对开发靶向细菌脂肪酸合酶的新分子产生了新的兴趣,这些分子可用于治疗细菌性疾病。在这篇综述中,我们着眼于人类和细菌中脂肪酸合成之间的差异和相似性,并重点介绍了各种小分子,它们已被证明可以抑制哺乳动物或细菌的脂肪酸合酶或两者。

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