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含丙二酸酯的新型查尔酮衍生物的合成、生物活性及作用机制研究。

Synthesis, Biological Activity and Action Mechanism Study of Novel Chalcone Derivatives Containing Malonate.

机构信息

State Key Laboratory Breeding Base of Green Pesticide and Agricultural Bioengineering, Center for Research and Development of Fine Chemicals, Guizhou University, Guiyang, 550025, P. R. China.

出版信息

Chem Biodivers. 2020 Apr;17(4):e2000025. doi: 10.1002/cbdv.202000025. Epub 2020 Mar 9.

Abstract

A series of novel chalcone malonate derivatives were synthesized and their antibacterial and antiviral activities were evaluated. All target compounds were characterized by spectral data. The results of antimicrobial bioassay showed that one compound (diethyl [3-(naphthalen-2-yl)-1-(3-nitrophenyl)-3-oxopropyl]propanedioate) showed excellent antibacterial activity against Xanthomonas oryzae pv. oryzae (Xoo), with an EC value of 10.2 μg/mL, which is significantly superior to bismerthiazol (71.7 μg/mL) and thiodiazole copper (97.8 μg/mL). At the same time, the mechanism of two compounds was confirmed by scanning electron microscopy. In addition, another compound (diethyl [3-(naphthalen-2-yl)-1-(4-nitrophenyl)-3-oxopropyl]propanedioate) showed significant curative activity to tobacco mosaic virus, with a value of 74.3 %, which was superior to 53.3 % of ningnanmycin. The results of microscale thermophoresis also showed that the Kd value of the combination of two compounds with the coat protein of tobacco mosaic virus was 0.211 and 0.166 μmol/L, which was better than 0.596 μmol/L of ningnanmycin. At the same time, the molecular docking of two compounds with tobacco mosaic virus-coat protein shows that the compound is well embedded in the pocket between the two subunits of tobacco mosaic virus-coat protein. These results show that chalcone derivatives containing malonate group can be considered as activators in the design of antibacterial and antiviral agents.

摘要

一系列新型查尔酮丙二酸酯衍生物被合成,并评估了它们的抗菌和抗病毒活性。所有目标化合物均通过光谱数据进行了表征。抗菌生物测定结果表明,一种化合物(二乙基[3-(萘-2-基)-1-(3-硝基苯基)-3-氧代丙基]丙二酸酯)对稻黄单胞菌(Xoo)表现出优异的抗菌活性,EC 值为 10.2μg/mL,明显优于双脒噻唑(71.7μg/mL)和噻二唑铜(97.8μg/mL)。同时,两种化合物的作用机制通过扫描电子显微镜得到了证实。此外,另一种化合物(二乙基[3-(萘-2-基)-1-(4-硝基苯基)-3-氧代丙基]丙二酸酯)对烟草花叶病毒表现出显著的治疗活性,活性值为 74.3%,优于宁南霉素的 53.3%。微量热泳动实验的结果也表明,两种化合物与烟草花叶病毒外壳蛋白结合的 Kd 值分别为 0.211 和 0.166μmol/L,优于宁南霉素的 0.596μmol/L。同时,两种化合物与烟草花叶病毒外壳蛋白的分子对接表明,化合物很好地嵌入了烟草花叶病毒外壳蛋白两个亚基之间的口袋中。这些结果表明,含有丙二酸酯基团的查尔酮衍生物可以作为设计抗菌和抗病毒药物的激活剂。

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