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[2,5,6-三取代-4(3H)嘧啶酮衍生物抗病毒化合物的合成及干扰素诱导活性研究]

[Synthesis and interferon-inducing activity studies on the antiviral compounds of 2,5,6-trisubstituted-4(3H) pyrimidinone derivatives].

作者信息

Liu X Y, Xu L J

机构信息

Department of Pharmacy, Shandong Medical University, Jinan.

出版信息

Yao Xue Xue Bao. 1994;29(2):153-7.

PMID:8042514
Abstract

In order to search for more ideal antiviral drugs, 21 substituted pyrimidinone derivatives were designed and synthesized, among which 11 were not reported before. The chemical structures were characterized by elemental and spectral analysis. The serum interferon-inducing activity was tested in mice. All 2-amino-5-bromo-6-substituted-4-(3H)pyrimidinone compounds were shown to have interferon inducing activity. The corresponding substituted pyrimidine thiones were less active. The new compounds of 6-sulfophenyl derivatives are soluble in water, but the interferon-inducing activity are not higher than the original compound of ABPP.

摘要

为了寻找更理想的抗病毒药物,设计并合成了21种取代嘧啶酮衍生物,其中11种未见报道。通过元素分析和光谱分析对其化学结构进行了表征。在小鼠体内测试了血清干扰素诱导活性。所有2-氨基-5-溴-6-取代-4-(3H)嘧啶酮化合物均显示出具有干扰素诱导活性。相应的取代嘧啶硫酮活性较低。6-磺苯基衍生物的新化合物可溶于水,但其干扰素诱导活性不高于ABPP的原化合物。

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