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Design, synthesis and in vitro PDE4 inhibition activity of certain quinazolinone derivatives for treatment of asthma

机译:某些喹唑啉酮衍生物的设计,合成及体外PDE4抑制活性对哮喘的治疗作用

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摘要

In this study, a novel series of quinazolinone derivatives analogue to nitraquazone structure were synthesized. The compounds tested for their inhibitory activity against phosphodiesterase 4B revealed that compound 6d shows promising inhibitory activity comparable to that of Rolipram, whereas compounds 6a and 6c exhibited moderate inhibitory activity.
机译:在这项研究中,合成了一系列新的喹唑啉酮衍生物类似的硝唑酮结构。经测试的化合物对磷酸二酯酶4B的抑制活性表明,化合物6d的抑制活性与罗利普兰相当,而化合物6a和6c表现出中等的抑制活性。

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