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芳基萘木脂素类化合物的合成及抗乙型肝炎病毒活性评价。

Synthesis and the biological evaluation of arylnaphthalene lignans as anti-hepatitis B virus agents.

机构信息

Institute of Biochemistry and Molecular Biology, National Yang-Ming University, Taipei, Taiwan, ROC.

出版信息

Bioorg Med Chem. 2010 Feb;18(3):1213-26. doi: 10.1016/j.bmc.2009.12.038. Epub 2009 Dec 21.

Abstract

We have previously shown that helioxanthin can suppress human hepatitis B virus gene expression. A series of helioxanthin analogues were synthesized and evaluated for their anti-hepatitis B virus activity. Modifications at the lactone rings and methylenedioxy unit of helioxanthin can modulate the antiviral activity. Among them, compound 32 is the most effective anti-HBV agent. Compound 32 can suppress the secretion of viral surface antigen and e antigen in HepA2 cells with EC(50) values of 0.06 and 0.14 microM, respectively. Compound 32 not only inhibited HBV DNA with wild-type and lamivudine-resistant strain but also suppressed HBV mRNA, core protein and viral promoters. In this study, a full account of the preparation, structure-activity relationships of helioxanthin analogues, and the possible mechanism of anti-HBV activity of this class of compounds are presented. This type of compounds possesses unique mode of action differing from existing therapeutic drugs. They are potentially new anti-HBV agents.

摘要

我们之前已经表明,叶黄素可以抑制乙型肝炎病毒基因的表达。我们合成了一系列叶黄素类似物,并对其抗乙型肝炎病毒活性进行了评估。叶黄素内酯环和亚甲二氧基单元的修饰可以调节抗病毒活性。其中,化合物 32 是最有效的抗 HBV 药物。化合物 32 能抑制 HepA2 细胞中病毒表面抗原和 e 抗原的分泌,EC(50)值分别为 0.06 和 0.14μM。化合物 32 不仅能抑制野生型和拉米夫定耐药株的 HBV DNA,还能抑制 HBV mRNA、核心蛋白和病毒启动子。在本研究中,我们详细介绍了叶黄素类似物的制备、构效关系,以及这类化合物抗 HBV 活性的可能机制。这类化合物具有不同于现有治疗药物的独特作用模式。它们可能是新型抗 HBV 药物。

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