Structure elucidation and NMR assignments for three anthraquinone derivatives from the marine fungus Fusarium sp. (No. ZH-210)

Copyright (c) 2009 John Wiley & Sons, Ltd.

Bibliographische Detailangaben
Veröffentlicht in:Magnetic resonance in chemistry : MRC. - 1985. - 47(2009), 4 vom: 02. Apr., Seite 362-5
1. Verfasser: Chen, Yiguang (VerfasserIn)
Weitere Verfasser: Cai, Xiaoling, Pan, Jiahui, Gao, Junping, Li, Jing, Yuan, Jie, Fu, Liwu, She, Zhigang, Lin, Yongcheng
Format: Online-Aufsatz
Sprache:English
Veröffentlicht: 2009
Zugriff auf das übergeordnete Werk:Magnetic resonance in chemistry : MRC
Schlagworte:Journal Article Research Support, Non-U.S. Gov't 1,4,5,6,7,9-hexahydroxy-2-methoxy-7-methyl-5,6,8,8a,9,10a-hexahydro-7,9-epoxyanthracen-10-one 1,4,6,7,9-pentahydroxy-2-methoxy-7-methyl-5,6,8,8a,9,10a-hexahydro-7,9-epoxyanthracen-10-one 1,4,6-trihydroxy-2-methoxy-7-methyl-5,6,8,8a,9,10a-hexahydro-7,9-epoxyanthracen-10-one Anthraquinones
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520 |a The structure elucidations and complete (1)H and (13)C NMR assignments are reported for three new anthraquinone derivatives: Fusaquinon A (1), B (2), and C (3) isolated from the fermentation medium of the marine fungus Fusarium sp. (No. ZH-210). HREIMS, Fourier transform infrared absorption spectrometry (FT-IR), NMR experiments including gCOSY, gHMQC, gHMBC, and NOESY were used for the determination of the structures and NMR spectral assignments. Preliminary pharmacological test showed that they exhibited low cytotoxic activity towards KB, KBv200, and MCF-7 cell lines 
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700 1 |a Cai, Xiaoling  |e verfasserin  |4 aut 
700 1 |a Pan, Jiahui  |e verfasserin  |4 aut 
700 1 |a Gao, Junping  |e verfasserin  |4 aut 
700 1 |a Li, Jing  |e verfasserin  |4 aut 
700 1 |a Yuan, Jie  |e verfasserin  |4 aut 
700 1 |a Fu, Liwu  |e verfasserin  |4 aut 
700 1 |a She, Zhigang  |e verfasserin  |4 aut 
700 1 |a Lin, Yongcheng  |e verfasserin  |4 aut 
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