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Antibacterial activity of flavonoids and their structure-activity relationship: An update review

机译:黄酮类化合物及其结构 - 活动关系的抗菌活性:更新审查

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Based on World Health Organization reports, resistance of bacteria to well-known antibiotics is a major global health challenge now and in the future. Different strategies have been proposed to tackle this problem including inhibition of multidrug resistance pumps and biofilm formation in bacteria and development of new antibiotics with novel mechanism of action. Flavonoids are a large class of natural compounds, have been extensively studied for their antibacterial activity, and more than 150 articles have been published on this topic since 2005. Over the past decade, some promising results were obtained with the antibacterial activity of flavonoids. In some cases, flavonoids (especially chalcones) showed up to sixfold stronger antibacterial activities than standard drugs in the market. Some synthetic derivatives of flavonoids also exhibited remarkable antibacterial activities with 20- to 80-fold more potent activity than the standard drug against multidrug-resistant Gram-negative and Gram-positive bacteria (including Escherichia coli, Pseudomonas aeruginosa, and Staphylococcus aureus). This review summarizes the ever changing information on antibacterial activity of flavonoids since 2005, with a special focus on the structure-activity relationship and mechanisms of actions of this broad class of natural compounds.
机译:基于世界卫生组织的报告,细菌对知名抗生素的抵抗是现在和未来的主要全球健康挑战。已经提出了不同的策略来解决这个问题,包括抑制多药耐药泵和细菌中的生物膜形成以及具有新抗生素的新抗生素的发展。黄酮类化合物是一类大类的天然化合物,已被广泛研究其抗菌活性,自2005年以来已经发表了超过150篇文章。在过去的十年中,在黄酮类化合物的抗菌活性获得了一些有希望的结果。在某些情况下,黄酮类化合物(尤其是Chalcones)显示出比市场上标准药物的抗菌活性更高。黄酮类化合物的一些合成衍生物也表现出显着的抗菌活性,比对多药耐革兰阴性和革兰氏阳性细菌的标准药物(包括大肠杆菌,假单胞菌Aerginosa和金黄色葡萄球菌)的标准药物具有20至80倍的抗菌活性。本综述总结了自2005年以来的有关黄酮类化合物抗菌活性的不断变化的信息,特别关注了这类广泛的天然化合物的结构 - 活动关系和作用机制。

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