化学
阿魏酸
苯丙素
乙醚
烟草花叶病毒
恶二唑
体内
立体化学
有机化学
生物合成
生物化学
病毒
酶
生物技术
病毒学
生物
作者
Feng He,Panpan Wei,Gang Yu,Shengxin Guo,Zhiguo Zheng,Shunhong Chen,Ali Dai,Renfeng Zhang,Zengxue Wu,Jian Wu
标识
DOI:10.1016/j.bioorg.2021.105248
摘要
A series of new ferulic acid derivatives bearing an oxadiazole ether was synthesized by introducing a structure of oxadiazole into trans-ferulic acid via an ether linkage. The synthesized target compounds were evaluated in vivo for their anti-TMV (tobacco mosaic virus) activity, which indicated that some synthesized compounds displayed strong activity for controlling TMV. For protective activity, compounds 6f and 6h had the most activities of 65% and 69.8% at 500 mg L-1, respectively. Compounds 6a, 6b, 6e, 6f and 6h showed > 60% curative activities at 500 mg L-1. Preliminary proteomics analysis showed that compound 6h could regulate the phenylpropanoid biosynthesis pathway and chloroplast function. These results indicated that synthesized novel ferulic acid derivatives could be used for controlling TMV.
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