Acanthiline A, a pyrido[1,2-a]indole alkaloid from Chinese mangrove Acanthus ilicifolius-Reference-Cited by-同舟云学术

Acanthiline A, a pyrido[1,2-a]indole alkaloid from Chinese mangrove Acanthus ilicifolius

Published:2018-06-27 Issue:11 Volume:20 Page:1088-1092
ISSN:1028-6020
Container-title:Journal of Asian Natural Products Research
language:en
Short-container-title:Journal of Asian Natural Products Research

Author:

Cai You-Sheng¹²,Sun Ji-Zheng³,Tang Qing-Qing¹,Fan Fengkai⁴,Guo Yue-Wei²⁵

Affiliation:

1. Institute of TCM and Natural Products, School of Pharmaceutical Sciences, Wuhan University, Wuhan 430071, China

2. State Key Laboratory of Drug Research, Shanghai Institute of Materia Medica, Chinese Academy of Sciences, Shanghai 201203, China

3. College of Life Science, Taishan Medical University, Taian 271016, China

4. Hubei Key Laboratory of Purification and Application of Plant Anti-Cancer Ingredients, College of Chemistry and Life Science, Hubei University of Education, Wuhan 430205, China

5. Open Studio for Druggability Research of Marine Lead Compounds, Qingdao National Laboratory for Marine Science and Technology, Qingdao 266237, China

Funder

National Natural Science Foundation of China

Natural Science Foundation of Hubei Province

open project of Hubei Key Laboratory of Purification and Application of Plant Anti-Cancer Ingredients

Hubei Key Laboratory of Purification and Application of Plant Anti-Cancer Ingredients

SKLDR/SIMM Project

NSFC-Shandong Joint Fund for Marine Science Research Centers

he open project of Hubei Key Laboratory of Purification and Application of Plant Anti-Cancer Ingredients

Publisher

Informa UK Limited

Subject

Organic Chemistry,Complementary and alternative medicine,Drug Discovery,Pharmaceutical Science,Pharmacology,Molecular Medicine,General Medicine,Analytical Chemistry

Link

https://www.tandfonline.com/doi/pdf/10.1080/10286020.2018.1488834

Reference18 articles.

1. Structure, bioactivities, biosynthetic relationships and chemical synthesis of the spirodioxynaphthalenes

2. Palmarumycins BG1−BG7 and Preussomerin BG1: Establishment of Their Absolute Configurations Using Theoretical Calculations of Electronic Circular Dichroism Spectra

3. Gymnorrhizol, an unusual macrocyclic polydisulfide from the Chinese mangrove Bruguiera gymnorrhiza

4. Total Synthesis of Gymnorrhizol, an Unprecedented 15-Membered Macrocyclic Polydisulfide from the Chinese Mangrove Bruguiera gymnorrhiza

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