Author:
Peng Weiwei,Huang Qi,Ke Xin,Wang Wenxuan,Chen Yan,Sang Zihuan,Chen Chen,Qin Siyu,Zheng Yuting,Tan Haibo,Zou Zhenxing
Abstract
AbstractTwo novel koninginin derivatives, koningipyridines A and B (1 and 2), along with four known compounds (3˗6) were isolated from the EtOAc extract of the endophytic fungus Trichoderma koningiopsis SC-5. Among them, koningipyridine A featured an unprecedented pentacyclic ketal skeleton with the formation of a fascinating 6/6/5/6/5 fused ring system and shared a characteristic pyridine core, which represents the first example of nitrogen-containing koninginin-type natural product. Moreover, koningipyridine B was the first member in the koninginin family sharing a unique 6/6/5 dihydropyridine skeleton, and it was suggested to be the critical biosynthetic precursor of koningipyridine A. The structures of 1 and 2 were elucidated by the interpretation of 1D and 2D NMR spectroscopy, HRESIMS data, as well as theoretical calculations of 13C NMR and electronic circular dichroism (ECD). Moreover, all isolates were screened for antimicrobial activities against Staphylococcus aureus, MRSA, and Escherichia coli as well as the cytotoxic effects against three cancer cell lines (A549, Hela, and HepG2).
Graphical Abstract
Funder
National Natural Science Foundation of China
Science and Technology Support Plan for Youth Innovation of Colleges and Universities of Shandong Province of China
Natural Science Foundation of Hunan Province
Jiangsu Provincial Key Research and Development Program
Central South University postgraduate independent exploration and innovation project
Publisher
Springer Science and Business Media LLC