Hybrid isoquinolines from Thalictrum foetidum: a new type of aporphine inhibiting Staphylococcus aureus by combined mechanisms-Reference-Cited by-同舟云学术

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

Published:2019 Issue:19 Volume:6 Page:3428-3434
ISSN:2052-4129
Container-title:Organic Chemistry Frontiers
language:en
Short-container-title:Org. Chem. Front.

Author:

Ding Cai-Feng¹²³⁴⁵,Zhang Rong-Ping⁶⁷⁸⁵,Yu Hao-Fei⁹¹⁰¹¹¹²¹³,Yang Jing¹²³⁴⁵,Qin Xu-Jie¹²³⁴⁵,Dai Zhi¹²³⁴⁵,Liu Ya-Ping¹²³⁴⁵,Lu Qiu-Min¹⁴¹⁵¹⁶⁵,Lai Ren¹⁴¹⁵¹⁶⁵,Luo Xiao-Dong¹²³⁴⁵^ORCID

Affiliation:

1. Key Laboratory of Phytochemistry and Plant Resources in West China

2. Kunming Institute of Botany

3. Chinese Academy of Sciences

4. Kunming 650201

5. People's Republic of China

6. School of Pharmaceutical Sciences and Yunnan Key Laboratory of Pharmacology for Natural Products

7. Kunming Medical University

8. Kunming 650500

9. Key Laboratory of Medicinal Chemistry for Natural Resource

10. Ministry of Education and Yunnan Province

11. School of Chemical Science and Technology

12. Yunnan University

13. Kunming 650091

14. Key Laboratory of Animal Models and Human Disease Mechanisms of Chinese Academy of Sciences & Yunnan Province

15. Kunming Institute of Zoology

16. Kunming 650223

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.

Funder

Ministry of Science and Technology of the People's Republic of China

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2019/QO/C9QO00737G

Reference51 articles.

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