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首页> 外文期刊>Chemical biology and drug design >Carbonic anhydrase inhibitors: Inhibition of human erythrocyte isozymes i and ii with a series of phenolic acids
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Carbonic anhydrase inhibitors: Inhibition of human erythrocyte isozymes i and ii with a series of phenolic acids

机译:碳酸酐酶抑制剂:用一系列酚酸抑制人红细胞同工酶i和ii

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摘要

The inhibitory effects of some phenolic acids on the cytosolic human carbonic anhydrase (hCA, EC 4.2.1.1) isozymes hCA I and hCA II were investigated. Ellagic acid, gallic acid, ferulic acid, caffeic acid, quercetin, p-coumaric acid, p-hydroxybenzoic acid, and syringic acid showed KI values in the range of 99-1061 μm for hCA I and of 105-758 μm against hCA II, respectively. Quercetin (for hCA I), p-coumaric acid (for hCA II), and gallic acid (for hCA II) exhibited competitive inhibitory effects with 4-nitrophenyl acetate as substrate. All of the other phenolic acids were found as non-competitive inhibitors with 4-nitrophenylacetate as substrate for hCA I and hCA II. The phenolic acids investigated here showed thus interesting hCA I and hCA II inhibitory effects and might be used as leads for generating enzyme inhibitors possibly targeting other CA isoforms which have not been yet assayed for their interactions with such agents.
机译:研究了某些酚酸对胞质人碳酸酐酶(hCA,EC 4.2.1.1)同工酶hCA I和hCA II的抑制作用。鞣花酸,没食子酸,阿魏酸,咖啡酸,槲皮素,对香豆酸,对羟基苯甲酸和丁香酸的KI值对于hCA I显示为KI值,相对于hCA II显示KI值为105-758μm , 分别。槲皮素(对于hCA I),对香豆酸(对于hCA II)和没食子酸(对于hCA II)在以乙酸4-硝基苯酯为底物时表现出竞争抑制作用。发现所有其他酚酸均为非竞争性抑制剂,其中乙酸4-硝基苯酯为hCA I和hCA II的底物。因此,这里研究的酚酸显示出令人感兴趣的hCA I和hCA II抑制作用,并且可以用作产生可能针对其他CA同种型的酶抑制剂的先导,这些同工酶尚未进行过与这类试剂的相互作用的分析。

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