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新型1,3,4-恶二唑/噻二唑-查耳酮缀合物的合成与抗病毒评估

Synthesis and antiviral evaluation of novel 1,3,4-oxadiazole/thiadiazole-chalcone conjugates.

作者信息

Gan Xiuhai, Hu Deyu, Chen Zhuo, Wang Yanjiao, Song Baoan

机构信息

State Key Laboratory Breeding Base of Green Pesticide and Agricultural Bioengineering, Key Laboratory of Green Pesticide and Agricultural Bioengineering, Ministry of Education, Research, and Development Center for Fine Chemicals, Guizhou University, Guiyang 550025, China; College of Chemistry and Life Science, Guizhou Education University, Guiyang 550018, China.

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

出版信息

Bioorg Med Chem Lett. 2017 Sep 15;27(18):4298-4301. doi: 10.1016/j.bmcl.2017.08.038. Epub 2017 Aug 18.

Abstract

A series of novel 1,3,4-oxadiazole/thiadiazole-chalcone conjugates were synthesized and their in vitro and in vivo antiviral activities were evaluated via microscale thermophoresis method and half-leaf method, respectively. The in vitro results indicated that compounds 7g, 7l, 8h, and 8l displayed good antiviral activity against TMV, with the binding constant values of 5.93, 6.15, 6.02, and 5.04μM, respectively, which were comparable to that of Ninnanmycin (6.78μM) and even better than that of Ribavirin (99.25μM). The in vivo results demonstrated that compounds 7g, 7l, 8h, and 8l exhibited remarkable anti-TMV activity with the EC values of 33.66, 33.97, 33.87 and 30.57µg/mL, respectively, which were comparable to that of Ningnanmycin (36.85µg/mL) and superior to that of Ribavirin (88.52µg/mL). Interestingly, the trend of antiviral activity in vivo was consistent with the in vitro results.

摘要

合成了一系列新型的1,3,4-恶二唑/噻二唑-查耳酮共轭物,并分别通过微量热泳法和半叶法对其体外和体内抗病毒活性进行了评估。体外实验结果表明,化合物7g、7l、8h和8l对烟草花叶病毒(TMV)表现出良好的抗病毒活性,其结合常数分别为5.93、6.15、6.02和5.04μM,与宁南霉素(6.78μM)相当,甚至优于利巴韦林(99.25μM)。体内实验结果表明,化合物7g、7l、8h和8l表现出显著的抗TMV活性,其半数有效浓度(EC)分别为33.66、33.97、33.87和30.57µg/mL,与宁南霉素(36.85µg/mL)相当,优于利巴韦林(88.52µg/mL)。有趣的是,体内抗病毒活性趋势与体外实验结果一致。

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