Journal
TETRAHEDRON
Volume 70, Issue 25, Pages 3859-3863Publisher
PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.tet.2014.04.043
Keywords
Penicillium sp.; Prenylated indole alkaloids; Mangrovamides; X-ray diffraction; Anti-acetylcholinesterase activity
Categories
Funding
- National Key Basic Research Program of China (973)'s Project [2010CB833800, 2011CB915503]
- National High Technology Research and Development Program (863 Program) [2012AA092104, 2013AA092901]
- National Natural Science Foundation of China [21302198, 31270402, 21172230, 30973679, 41376162, 41176148]
- Knowledge Innovation Program of Chinese Academy of Science [SQ201117, SQ201019]
- Guangdong Province-CAS Joint Research Program [2011B090300023, 2012B091100264]
- Guangdong Marine Economic Development and Innovation of Regional Demonstration Project [GD2012-D01-001, GD2012-D01-002]
Ask authors/readers for more resources
Three diprenylated indole alkaloids, mangrovamides A-C (1-3), featured a bicyclo [2.2.2] diazaoctane core and possessed a novel gamma-methyl proline and isoprene derived dimethyl gamma-pyrone functionalities hitherto unknown among the family of paraherquamides, were isolated from the fungus Penicillium sp., which was separated from a mangrove soil sample. The structures were elucidated based on NMR, X-ray, and CD methods. The possible biosynthetic pathway of these compounds is proposed. (C) 2014 Elsevier Ltd. All rights reserved.
Authors
I am an author on this paper
Click your name to claim this paper and add it to your profile.
Reviews
Recommended
No Data Available
Share Paper
