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含1,3,4-噻二唑部分的新型1,4-戊二烯-3-酮衍生物的合成及其抗病毒活性

Synthesis and Antiviral Activity of Novel 1,4-Pentadien-3-one Derivatives Containing a 1,3,4-Thiadiazole Moiety.

作者信息

Yu Lu, Gan Xiuhai, Zhou Dagui, He Fangcheng, Zeng Song, Hu Deyu

机构信息

State Key Laboratory Breeding Base of Green Pesticide and Agricultural Bioengineering, Key Laboratory of Green Pesticide and Agriculture Bioengineering, Ministry of Education, Guizhou University, Guiyang 550025, Guizhou, China.

出版信息

Molecules. 2017 Apr 21;22(4):658. doi: 10.3390/molecules22040658.

Abstract

1,4-Pentadien-3-one derivatives derived from curcumin possess excellent inhibitory activity against plant viruses. On the basis of this finding, a series of novel 1,4-pentadien-3-one derivatives containing a 1,3,4-thiadiazole moiety were designed and synthesized, and their structures confirmed by IR, ¹H-NMR, and C-NMR spectroscopy and elemental analysis. The antiviral activities of the title compounds were evaluated against tobacco mosaic virus (TMV) and cucumber mosaic virus (CMV) in vivo. The assay results showed that most of compounds had remarkable antiviral activities against TMV and CMV, among which compounds , , , , , and exhibited good curative, protection, and inactivation activity against TMV. Compounds , , , , , and exhibited excellent protection activity against TMV, with EC values of 105.01, 254.77, 135.38, 297.40, 248.18, and 129.87 μg/mL, respectively, which were superior to that of ribavirin (457.25 µg/mL). In addition, preliminary SARs indicated that small electron-withdrawing groups on the aromatic ring were favorable for anti-TMV activity. This finding suggests that 1,4-pentadien-3-one derivatives containing a 1,3,4-thiadiazole moiety may be considered as potential lead structures for discovering new antiviral agents.

摘要

源自姜黄素的1,4 - 戊二烯 - 3 - 酮衍生物对植物病毒具有优异的抑制活性。基于这一发现,设计并合成了一系列含有1,3,4 - 噻二唑部分的新型1,4 - 戊二烯 - 3 - 酮衍生物,并通过红外光谱、¹H - NMR、C - NMR光谱和元素分析对其结构进行了确证。在体内对目标化合物针对烟草花叶病毒(TMV)和黄瓜花叶病毒(CMV)的抗病毒活性进行了评估。测定结果表明,大多数化合物对TMV和CMV具有显著的抗病毒活性,其中化合物 、 、 、 、 和 对TMV表现出良好的治疗、保护和钝化活性。化合物 、 、 、 、 和 对TMV表现出优异的保护活性,其EC值分别为105.01、254.77、135.38、297.40、248.18和129.87 μg/mL,优于利巴韦林(457.25 µg/mL)。此外,初步的构效关系表明,芳环上的小吸电子基团有利于抗TMV活性。这一发现表明,含有1,3,4 - 噻二唑部分的1,4 - 戊二烯 - 3 - 酮衍生物可被视为发现新型抗病毒剂的潜在先导结构。

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