Issue 19, 2019

Hybrid isoquinolines from Thalictrum foetidum: a new type of aporphine inhibiting Staphylococcus aureus by combined mechanisms

Abstract

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.

Graphical abstract: Hybrid isoquinolines from Thalictrum foetidum: a new type of aporphine inhibiting Staphylococcus aureus by combined mechanisms

Supplementary files

Article information

Article type
Research Article
Submitted
06 Jun 2019
Accepted
05 Aug 2019
First published
29 Aug 2019

Org. Chem. Front., 2019,6, 3428-3434

Hybrid isoquinolines from Thalictrum foetidum: a new type of aporphine inhibiting Staphylococcus aureus by combined mechanisms

C. Ding, R. Zhang, H. Yu, J. Yang, X. Qin, Z. Dai, Y. Liu, Q. Lu, R. Lai and X. Luo, Org. Chem. Front., 2019, 6, 3428 DOI: 10.1039/C9QO00737G

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