Hybrid isoquinolines from Thalictrum foetidum: a new type of aporphine inhibiting Staphylococcus aureus by combined mechanisms
Ding, CF; Zhang, RP; Yu, HF; Yang, J; Qin, XJ; Dai, Z; Liu, YP; Lu, QM; Lai, R; Luo, XD
2019
发表期刊ORGANIC CHEMISTRY FRONTIERS
ISSN2052-4129
卷号6期号:19页码:3428-3434
摘要Thalfoetines A-D (1-4), unique hybrid aporphine alkaloids with a C-7 aromatic unit formed by a new C-C bond linking two building blocks, were isolated from Thalictrum foetidum. Their structures were elucidated by extensive spectroscopic and computational analysis. They inhibited bacteria significantly, and compound 1 damaged the cell structure of Staphylococcus aureus and inhibited its DNA synthesis.
收录类别SCI
语种英语
文献类型期刊论文
条目标识符http://ir.kiz.ac.cn/handle/152453/13030
专题科研部门_天然药物功能蛋白质学科组(赖仞)
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Ding, CF,Zhang, RP,Yu, HF,et al. Hybrid isoquinolines from Thalictrum foetidum: a new type of aporphine inhibiting Staphylococcus aureus by combined mechanisms[J]. ORGANIC CHEMISTRY FRONTIERS,2019,6(19):3428-3434.
APA Ding, CF.,Zhang, RP.,Yu, HF.,Yang, J.,Qin, XJ.,...&Luo, XD.(2019).Hybrid isoquinolines from Thalictrum foetidum: a new type of aporphine inhibiting Staphylococcus aureus by combined mechanisms.ORGANIC CHEMISTRY FRONTIERS,6(19),3428-3434.
MLA Ding, CF,et al."Hybrid isoquinolines from Thalictrum foetidum: a new type of aporphine inhibiting Staphylococcus aureus by combined mechanisms".ORGANIC CHEMISTRY FRONTIERS 6.19(2019):3428-3434.
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