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首页> 外文期刊>Medicinal chemistry research: an international journal for rapid communications on design and mechanisms of action of biologically active agents >Screening of a library of 4-aryl/heteroaryl-4H-fused pyrans for xanthine oxidase inhibition: synthesis, biological evaluation and docking studies
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Screening of a library of 4-aryl/heteroaryl-4H-fused pyrans for xanthine oxidase inhibition: synthesis, biological evaluation and docking studies

机译:筛选用于抑制黄嘌呤氧化酶的4-芳基/杂芳基-4H融合的吡喃文库:合成,生物学评估和对接研究

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摘要

A series of 4-aryl/heteroaryl-4H-fused pyrans was synthesized via multicomponent reaction in a microwave synthesizer. All the pyrans were evaluated for in vitro xanthine oxidase inhibition. Structure-activity relationship was also established. Among the series of 108 compounds, Compound 5n was the most potent displaying remarkable inhibition against the enzyme with an IC50 value of 0.59 mu M. Enzyme kinetic study was carried out for the compound 5n to determine the type of inhibition. The study revealed that the compound 5n was a mixed-type inhibitor. Molecular modelling studies were also performed to figure out the interactions of both the enantiomers of 5n with the amino acid residues of the enzyme.
机译:通过在微波合成器中的多组分反应,合成了一系列4-芳基/杂芳基-4H稠合的吡喃。评价所有吡喃的体外黄嘌呤氧化酶抑制作用。还建立了构效关系。在这108种化合物中,化合物5n对酶的抑制作用最强,IC50值为0.59μM。对化合物5n进行了酶动力学研究,以确定抑制的类型。研究表明,化合物5n是一种混合型抑制剂。还进行了分子建模研究,以弄清5n的两个对映异构体与酶的氨基酸残基之间的相互作用。

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