硫醚
恶二唑
化学
体内
杨梅素
EC50型
组合化学
立体化学
药物化学
有机化学
体外
生物化学
生物
抗氧化剂
山奈酚
生物技术
槲皮素
作者
Feng Peng,Tingting Liu,Qifan Wang,Fang Liu,Xiao Cao,Jinsong Yang,Liwei Liu,Chengwei Xie,Wei Xue
标识
DOI:10.1021/acs.jafc.1c03755
摘要
Various 1,3,4-oxadiazole thioether 4H-chromen-4-one derivatives were conceived. The title compounds demonstrated striking inhibitory effects against Xac, Psa, and Xoo. EC50 data exhibited that A8 (19.7 μg/mL) had better antibacterial activity against Xoo than myricetin, BT, and TC. Simultaneously, the mechanism of action of A8 had been verified by SEM. The results of anti-tobacco mosaic virus indicated that A9 had the best in vivo antiviral effect compared with ningnanmycin. From the data of MST, it could be seen that A9 (0.003 ± 0.001 μmol/L) exhibited a strong binding capacity, which was far superior to ningnanmycin (2.726 ± 1.301 μmol/L). This study shows that the 1,3,4-oxadiazole thioether 4H-chromen-4-one derivatives may become agricultural drugs with great potential.
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