Yuan Chao, Yang Hong-Xia, Guo Yu-Hua, Fan Lin, Zhang Ying-Bo, Li Gang
Tropical Crops Genetic Resources Institute, Chinese Academy of Tropical Agricultural Sciences CATAS Haikou 571101 People's Republic of China.
Department of Natural Medicinal Chemistry and Pharmacognosy, School of Pharmacy, Qingdao University Qingdao 266021 People's Republic of China
RSC Adv. 2019 Sep 2;9(47):27419-27423. doi: 10.1039/c9ra05308e. eCollection 2019 Aug 29.
Four new α-pyrones, hypotiens A-D (1-4), were isolated from a fungal endophyte, J2, harbored in the medicinal plant . Their structures were determined through detailed HRMS and NMR spectroscopic data. Compounds 1-4 are new α-pyrone derivatives containing an unusual dimethyl substitution in the highly unsaturated side chain. Their plausible biosynthetic pathway was discussed. Biological assay indicated that compounds 1-4 showed no antimicrobial, quorum sensing inhibitory, and cytotoxic activities. The specific side chain in α-pyrone derivatives 1-4 might be responsible for the weak pharmacological activities.
从药用植物中分离得到的一株内生真菌J2中,分离出了4个新的α-吡喃酮类化合物,即低张力素A-D(1-4)。通过详细的高分辨质谱和核磁共振光谱数据确定了它们的结构。化合物1-4是新的α-吡喃酮衍生物,在高度不饱和侧链中含有不寻常的二甲基取代。讨论了它们可能的生物合成途径。生物活性测定表明,化合物1-4没有抗菌、群体感应抑制和细胞毒性活性。α-吡喃酮衍生物1-4中特定的侧链可能是其药理活性较弱的原因。