抗真菌
异黄酮素
化学
植物
传统医学
生物
微生物学
生物化学
医学
作者
Cheng-Feng Liu,Jianguo Tan,Xuye Wu,Cai-Yan Tian,Qiao An,Ping Yi,Xiao‐Jiang Hao,Zhan‐Xing Hu
标识
DOI:10.1021/acs.jafc.5c00617
摘要
In order to discover novel fungicides from natural products, the phytochemical investigation of Thermopsis lanceolata seeds was thoroughly conducted. Eight new isoflavone derivatives (1-5 and 8-10), two new stilbenes (6 and 7), as well as 21 known isoflavones (11-31) were obtained from the crude extract of T. lanceolata seeds following a bioassay-guided method. The structures of 1-31 were confirmed via HRESIMS, NMR, IR, UV, and quantum chemistry calculations. The antifungal activities of 1-31 against Phytophthora nicotiana, Colletotrichum orbiculare, Rhizoctonia solani, and Botrytis cinerea were screened according to the mycelial inhibition test. Compound 6 displayed significant antifungal activity against B. cinerea in vitro (EC50: 9.68 μg/mL) and had an 8 5.7% prevention and control effect in vivo (100 μg/mL). Moreover, antifungal mechanism studies revealed that 6 causes the accumulation of reactive oxygen species, increases the level of lipid peroxidation, decreases the activity of MDH, and finally triggers molecular damage and cell death in vitro. Therefore, 6 can be utilized as a lead compound for novel fungicides.
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