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

被引:112
作者
Gan, Xiuhai [1 ,2 ]
Hu, Deyu [1 ]
Chen, Zhuo [1 ]
Wang, Yanjiao [1 ]
Song, Baoan [1 ]
机构
[1] Guizhou Univ, State Key Lab Breeding Base Green Pesticide & Agr, Key Lab Green Pesticide & Agr Bioengn, Minist Educ,Res & Dev Ctr Fine Chem, Guiyang 550025, Guizhou, Peoples R China
[2] Guizhou Educ Univ, Coll Chem & Life Sci, Guiyang 550018, Guizhou, Peoples R China
基金
中国国家自然科学基金;
关键词
Chalcone; 1,3,4-Oxadiazole/thiadiazole; Tobacco mosaic virus coat protein; Antiviral activity; Microscale thermophoresis; TOBACCO-MOSAIC-VIRUS; 1,3,4-OXADIAZOLE MOIETY; ANTIBACTERIAL ACTIVITY; BIOLOGICAL EVALUATION; CHALCONE DERIVATIVES; ANTICANCER AGENTS; MOLECULAR DOCKING; COAT PROTEIN; DESIGN; HYBRIDS;
D O I
10.1016/j.bmcl.2017.08.038
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
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 5.04 mu M, respectively, which were comparable to that of Ninnanmycin (6.78 mu M) and even better than that of Ribavirin (99.25 mu M). The in vivo results demonstrated that compounds 7g, 7l, 8h, and 8l exhibited remarkable anti-TMV activity with the EC50 values of 33.66, 33.97, 33.87 and 30.57 mu g/mL, respectively, which were comparable to that of Ningnanmycin (36.85 mu g/mL) and superior to that of Ribavirin (88.52 mu g/mL). Interestingly, the trend of antiviral activity in vivo was consistent with the in vitro results. (C) 2017 Elsevier Ltd. All rights reserved.
引用
收藏
页码:4298 / 4301
页数:4
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