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Synthesis and Antiviral Bioactivities of 2-Aryl- or 2-Methyl-3-(substituted- Benzalamino)-4(3H)-quinazolinone Derivatives

机译:2-芳基或2-甲基-3-(取代的苯甲氨基)-4(3H)-喹唑啉酮衍生物的合成及抗病毒活性

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摘要

A simple and general method has been developed for the synthesis of various 4(3H)-quinazolinone derivatives by the treatment of the appropriate 3-amino-2-aryl-4(3H)-quinazolinone with a substituted benzaldehyde in ethanol. The structures of the compounds were characterized by elemental analysis, IR, 1H-NMR and 13C-NMR spectra. The title 2-aryl- or 2-methyl-3-(substituted-benzalamino)-4(3H)-quinazolinone compounds >III-1~>III-31 were found to possess moderate to good antiviral activity. Semi-quantitative PCR and Real Time PCR assays were used to ascertain the target of action of compound >III-31 against TMV. The studies suggest that >III-31 possesses antiviral activity due to induction of up-regulation of PR-1a and PR-5, thereby inhibiting virus proliferation and movement by enhancement of the activity of some defensive enzyme.
机译:通过在乙醇中用取代的苯甲醛处理适当的3-氨基-2-芳基-4(3H)-喹唑啉酮,已开发出一种简单且通用的合成各种4(3H)-喹唑啉酮衍生物的方法。通过元素分析,IR, 1 H-NMR和 13 C-NMR谱对化合物的结构进行表征。发现标题> III-1 〜> III-31 的标题为2-芳基或2-甲基-3-(取代的苯甲氨基)-4(3H)-喹唑啉酮化合物具有中等至良好的抗病毒活性。使用半定量PCR和实时PCR方法确定化合物> III-31 对TMV的作用目标。研究表明,> III-31 具有抗病毒活性,原因是诱导PR-1a和PR-5的上调,从而通过增强某些防御酶的活性来抑制病毒的增殖和运动。

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