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Inhibition of the β-carbonic anhydrase from the dandruff-producing fungus Malassezia globosa with monothiocarbamates

机译:单硫代氨基甲酸盐对头皮屑产生性球孢马拉色菌中β-碳酸酐酶的抑制作用

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摘要

A series of monothiocarbamates (MTCs) was investigated for the inhibition of the β-class carbonic anhydrase (CAs, EC 4.2.1.1) from the fungal parasite Malassezia globosa, MgCA. These MTCs incorporate various scaffolds, among which aliphatic amine with 1–4 carbons atom in their molecule, morpholine, piperazine, as well as phenethylamine and benzylamine derivatives. All the reported MTCs displayed a better efficacy in inhibiting MgCA compared to the clinically used sulphonamide drug acetazolamide (KI of 74 μM), with KIs spanning between 1.85 and 18.9 μM. The homology model of the enzyme previously reported by us was used to rationalize the results by docking some of these MTCs within the fungal CA active site. This study might be useful to enrich the knowledge of the MgCA inhibition profile, eliciting novel ideas pertaining the design of modulators with potential efficacy in combatting dandruff or other fungal infections.
机译:研究了一系列单硫代氨基甲酸酯(MTCs)对真菌寄生虫MalCA球菌的β-类碳酸酐酶(CAs,EC 4.2.1.1)的抑制作用。这些MTC包含各种支架,其中包括分子中具有1-4个碳原子的脂族胺,吗啉,哌嗪以及苯乙胺和苄胺衍生物。与临床上使用的磺酰胺类药物乙酰唑胺(KI为74?μM)相比,所有报道的MTC均显示出更好的抑制MgCA的功效,KI的范围为1.85至18.9μM。我们先前报道的酶的同源性模型用于通过将这些MTC中的一些停靠在真菌CA活性位点内来合理化结果。这项研究可能有助于丰富MgCA抑制谱的知识,从而激发出与调节头皮屑或其他真菌感染具有潜在功效的调节剂设计有关的新思路。

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