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Inhibition of anthrax lethal factor by curcumin and chemically modified curcumin derivatives

机译:姜黄素和化学修饰的姜黄素衍生物对炭疽致死因子的抑制作用

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摘要

Curcuma longaCurcumin (diferuloylmethane), the active ingredient in the eastern spice turmeric (Curcuma longa), has been shown to inhibit the activities of numerous enzymes and signaling molecules involved in cancer, bacterial and viral infections and inflammatory diseases. We have investigated the inhibitory activities of curcumin and chemically modified curcumin (CMC) derivatives toward lethal factor (LF), the proteolytic component of anthrax toxin produced by the bacterium Bacillus anthracis. Curcumin (Compound >1) appears to inhibit the catalytic activity of LF through a mixture of inhibitory mechanisms, without significant compromise to the binding of oligopeptide substrates, and one CMC derivative in particular, Compound >3 (4-phenylaminocarbonylbis-demethoxycurcumin), is capable of inhibiting LF with potency comparable with the parent compound, while also showing improved solubility and stability. The quantitative reduction in catalytic activity achieved by the different CMC derivatives appears to be a function of the proportion of the multiple mechanisms through which they inhibit the enzyme.
机译:姜黄素姜黄素(二氟甲酰甲烷)是东部香料姜黄(姜黄素)中的活性成分,已显示出抑制多种酶和信号分子的活性,这些酶和信号分子参与癌症,细菌和病毒感染以及炎性疾病。我们研究了姜黄素和化学修饰的姜黄素(CMC)衍生物对致死因子(LF)的抑制活性,所述致死因子是由炭疽杆菌产生的炭疽毒素的蛋白水解成分。姜黄素(化合物> 1 )似乎可以通过多种抑制机制来抑制LF的催化活性,而不会显着影响寡肽底物的结合,特别是一种CMC衍生物化合物> 3 < (4-苯基氨基羰基双-去甲氧基姜黄素)能够以与母体化合物相当的效力抑制LF,同时还显示出改善的溶解性和稳定性。由不同的CMC衍生物实现的催化活性的定量降低似乎是它们抑制酶的多种机理的比例的函数。

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