Planta Med 2012; 78(17): 1861-1866
DOI: 10.1055/s-0032-1315395
Natural Product Chemistry
Original Papers
Georg Thieme Verlag KG Stuttgart · New York

Cytotoxic Polyphenols from the Fungus Penicillium expansum 091 006 Endogenous with the Mangrove Plant Excoecaria agallocha

Junfeng Wang*
1   Key Laboratory of Marine Drugs, Ministry of Education of China, School of Medicine and Pharmacy, Ocean University of China, Qingdao, P. R. China
,
Zhenyu Lu*
1   Key Laboratory of Marine Drugs, Ministry of Education of China, School of Medicine and Pharmacy, Ocean University of China, Qingdao, P. R. China
,
Peipei Liu
1   Key Laboratory of Marine Drugs, Ministry of Education of China, School of Medicine and Pharmacy, Ocean University of China, Qingdao, P. R. China
,
Yi Wang
1   Key Laboratory of Marine Drugs, Ministry of Education of China, School of Medicine and Pharmacy, Ocean University of China, Qingdao, P. R. China
,
Jing Li
1   Key Laboratory of Marine Drugs, Ministry of Education of China, School of Medicine and Pharmacy, Ocean University of China, Qingdao, P. R. China
,
Kui Hong
2   Key Laboratory of Combinatorial Biosynthesis and Drug Discovery, Ministry of Education of China, School of Pharmaceutical Sciences, Wuhan University, Wuhan, P. R. China
,
Weiming Zhu
1   Key Laboratory of Marine Drugs, Ministry of Education of China, School of Medicine and Pharmacy, Ocean University of China, Qingdao, P. R. China
› Author Affiliations
Further Information

Publication History

received 18 May 2012
revised 20 July 2012

accepted 27 August 2012

Publication Date:
11 October 2012 (online)

Abstract

As part of our ongoing chemical investigation of biologically active metabolites from marine-derived fungi, four new polyphenols containing both phenolic bisabolane and diphenyl ether units, expansols C–F (14), and one new diphenyl ether derivative, 3-O-methyldiorcinol (5), as well as twelve known compounds (617), were isolated from Penicillium expansum 091006 endogenous with the mangrove plant Excoecaria agallocha (Euphorbiaceae). The structures of the new metabolites were determined on the basis of NMR and mass spectroscopy. Among them, expansols C (1) and E (3) exhibited weak cytotoxicity against the HL-60 cell lines with IC50 values of 18.2 and 20.8 µM, respectively. The results showed that diphenyl ether substituted phenolic bisabolanes with a Δ7 double bond in the side chain are slightly less cytotoxic to HL-60 cell lines than the 7-OH or 7-OCH3 derivatives.

* These authors contributed equally to this work.


Supporting Information

 
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