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231224s2012 xx |||||o 00| ||eng c |
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|a 10.1002/mrc.3790
|2 doi
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|a pubmed24n0717.xml
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|a (NLM)22314503
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|a DE-627
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|e rakwb
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|a eng
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|a Hwang, Doseok
|e verfasserin
|4 aut
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|a Synthesis of methoxybenzoflavones and assignments of their NMR data
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|c 2012
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|a Text
|b txt
|2 rdacontent
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|a ƒaComputermedien
|b c
|2 rdamedia
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|a ƒa Online-Ressource
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|2 rdacarrier
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|a Date Completed 23.08.2012
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|a Date Revised 07.03.2012
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|a published: Print-Electronic
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|a Citation Status MEDLINE
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|a Copyright © 2012 John Wiley & Sons, Ltd.
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|a A phytotoxic root exudate from Acroptilon repens was identified as 7,8-benzoflavone, an inhibitor of cytochrome P450 1A2 and activator of cytochrome P450 3A4. The synthetic 5,6-benzoflavone also is a potent phytotoxin. Six 7,8-benzoflavones and eight 5,6-benzoflavones were synthesized in this study. The NMR data for a few of these compounds have been previously reported; however, the NMR data for most of them have not been reported. For reference purposes, the complete NMR data for the 14 benzoflavones are described
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|a Journal Article
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|a Research Support, Non-U.S. Gov't
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|a Benzoflavones
|2 NLM
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|a Jo, Geunhyeong
|e verfasserin
|4 aut
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|a Hyun, Jiye
|e verfasserin
|4 aut
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|a Lee, Sung Dae
|e verfasserin
|4 aut
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|a Koh, Dongsoo
|e verfasserin
|4 aut
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|a Lim, Yoongho
|e verfasserin
|4 aut
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|i Enthalten in
|t Magnetic resonance in chemistry : MRC
|d 1985
|g 50(2012), 1 vom: 09. Jan., Seite 62-7
|w (DE-627)NLM098179667
|x 1097-458X
|7 nnns
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|g volume:50
|g year:2012
|g number:1
|g day:09
|g month:01
|g pages:62-7
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|u http://dx.doi.org/10.1002/mrc.3790
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