Ervatamines A–I, Anti-inflammatory Monoterpenoid Indole Alkaloids with Diverse Skeletons from Ervatamia hainanensis-Reference-Cited by-同舟云学术

Ervatamines A–I, Anti-inflammatory Monoterpenoid Indole Alkaloids with Diverse Skeletons from Ervatamia hainanensis

Published:2015-05-29 Issue:6 Volume:78 Page:1253-1261
ISSN:0163-3864
Container-title:Journal of Natural Products
language:en
Short-container-title:J. Nat. Prod.

Author:

Zhang Dong-Bo¹,Yu Dao-Geng²,Sun Meng¹,Zhu Xu-Xin¹,Yao Xiao-Jun¹,Zhou Shuang-Yan¹,Chen Jian-Jun¹,Gao Kun¹

Affiliation:

1. State Key Laboratory of Applied Organic Chemistry, College of Chemistry and Chemical Engineering, Lanzhou University, Lanzhou 730000, People’s Republic of China

2. Tropical Crops Genetic Resources Institute, Chinese Academy of Tropical Agricultural Science, Danzhou 571737, People’s Republic of China

Funder

National Natural Science Foundation of China

Ministry of Education of the People's Republic of China

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

State Administration of Foreign Experts Affairs

Publisher

American Chemical Society (ACS)

Subject

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

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.jnatprod.5b00051

Reference33 articles.

1. Guangdong Nonglin College. In Chinese Flora (ZhongguoZhiwuZhi);Science Press:Beijing, 1977; Vol.63, pp98,112–114.

2. A new indole alkaloid from Ervatamia yunnanensis

3. Structure, biological activity, and a biomimetic partial synthesis of the lirofolines, novel pentacylic indole alkaloids from Tabernaemontana

4. Biscarpamontamines A and B, an Aspidosperma−Iboga Bisindole Alkaloid and an Aspidosperma−Aspidosperma Bisindole Alkaloid, from Tabernaemontana sphaerocarpa

5. Cytotoxic Indole Alkaloids from Tabernaemontana divaricata

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