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231223s2009 xx |||||o 00| ||eng c |
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|a 10.1002/mrc.2391
|2 doi
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|a pubmed25n0620.xml
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|a DE-627
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|a eng
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|a Chen, Yiguang
|e verfasserin
|4 aut
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|a Structure elucidation and NMR assignments for three anthraquinone derivatives from the marine fungus Fusarium sp. (No. ZH-210)
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|c 2009
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|a Text
|b txt
|2 rdacontent
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|a ƒaComputermedien
|b c
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|a ƒa Online-Ressource
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|a Date Completed 12.05.2009
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|a Date Revised 10.03.2009
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|a published: Print
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|a Citation Status MEDLINE
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|a Copyright (c) 2009 John Wiley & Sons, Ltd.
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|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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|a Journal Article
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|a Research Support, Non-U.S. Gov't
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|a 1,4,5,6,7,9-hexahydroxy-2-methoxy-7-methyl-5,6,8,8a,9,10a-hexahydro-7,9-epoxyanthracen-10-one
|2 NLM
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|a 1,4,6,7,9-pentahydroxy-2-methoxy-7-methyl-5,6,8,8a,9,10a-hexahydro-7,9-epoxyanthracen-10-one
|2 NLM
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|a 1,4,6-trihydroxy-2-methoxy-7-methyl-5,6,8,8a,9,10a-hexahydro-7,9-epoxyanthracen-10-one
|2 NLM
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|a Anthraquinones
|2 NLM
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|a Cai, Xiaoling
|e verfasserin
|4 aut
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1 |
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|a Pan, Jiahui
|e verfasserin
|4 aut
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1 |
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|a Gao, Junping
|e verfasserin
|4 aut
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|a Li, Jing
|e verfasserin
|4 aut
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|a Yuan, Jie
|e verfasserin
|4 aut
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|a Fu, Liwu
|e verfasserin
|4 aut
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|a She, Zhigang
|e verfasserin
|4 aut
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|a Lin, Yongcheng
|e verfasserin
|4 aut
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|i Enthalten in
|t Magnetic resonance in chemistry : MRC
|d 1985
|g 47(2009), 4 vom: 02. Apr., Seite 362-5
|w (DE-627)NLM098179667
|x 1097-458X
|7 nnns
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|g volume:47
|g year:2009
|g number:4
|g day:02
|g month:04
|g pages:362-5
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|u http://dx.doi.org/10.1002/mrc.2391
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