Dihydroanthracenone metabolites from the endophytic fungus Diaporthe melonis isolated from Annona squamosa

被引:25
作者
Ola, Antonius R. B. [1 ,2 ]
Debbab, Abdessamad [1 ]
Kurtan, Tibor [3 ]
Broetz-Oesterhelt, Heike [1 ]
Aly, Amal H. [1 ]
Proksch, Peter [1 ]
机构
[1] Univ Dusseldorf, Inst Pharmazeut Biol & Biotechnol, D-40225 Dusseldorf, Germany
[2] Nusa Cendana Univ, Fac Sci & Engn, Dept Chem, Kupang 85001, Indonesia
[3] Univ Debrecen, Dept Organ Chem, H-4010 Debrecen, Hungary
关键词
Annona squamosa; Antibacterial activity; Dihydroanthracenones; Diaporthe melonis; Endophytic fungus; AUSTRALIAN TOADSTOOLS; PIGMENTS; ANTHRAQUINONES; ACETOGENINS; STEREOCHEMISTRY; SEEDS;
D O I
10.1016/j.tetlet.2014.03.110
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Chemical investigation of the endophytic fungus Diaporthe melonis, isolated from Annona squamosa, yielded two new dihydroanthracenone atropodiastereomers, diaporthemins A (1) and B (2), together with the known flavomannin-6,6 '-di-O-methyl ether (3). The structures of the new compounds were established on the basis of extensive 1D and 2D NMR spectroscopy, as well as by high resolution mass spectrometry and by CD spectroscopy. Compounds 1-3 were tested for their antimicrobial activity against a multi-resistant clinical isolate of Staphylococcus aureus 25697, a susceptible reference strain of S. aureus ATCC 29213 and against Streptococcus pneumoniae ATCC 49619. Compound 3 strongly inhibited S. pneumonia growth with a MIC value of 2 mu g/mL, and showed moderate activity against the S. aureus multi-resistant clinical isolate and susceptible reference strain (MIC 32 mu g/mL), whereas 1 and 2 were not active against the tested strains. (C) 2014 Elsevier Ltd. All rights reserved.
引用
收藏
页码:3147 / 3150
页数:4
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