Category:FLN

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#REDIRECT [[:Category:Flindersiaceae]]
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{{Huge|Neoflavonoid}}
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{{Hierarchy|{{PAGENAME}}}}
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=={{Bilingual|ネオフラボノイドの概要|Overview}}==
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{| class="wikitable" border="1" cellspacing="0"
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|-
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! colspan="6"|2nd Class
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|-
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|FLNA||[[:Category:FLNA|4-Arylcoumarin]]<br>[[Image:Flna.png|72px]]
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|FLNB||[[:Category:FLNB|4-Arylchroman]]<br>[[Image:Flnb.png|72px]]
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|FLNC||[[:Category:FLNC|Dalbergiquinol]]<br>[[Image:Flnc.png|72px]]
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|-
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|FLND||[[:Category:FLND|Dalbergione]]<br>[[Image:Flnd.png|65px]]
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|FLNE||[[:Category:FLNE|Neoflavene]]<br>[[Image:Flne.png|50px]]
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|FLNF||[[:Category:FLNF|Coumarinic acid]]<br>[[Image:Flnf.png|72px]]
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|}
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=={{Bilingual|データベース統計|Database statistics}}==<!--- see FL1--->
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{{#def:FLN|{{#SearchTitle:FLN|}}}}
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{{#def:rFLN|{{#SearchLine:&&FLN|Reference}}}}
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{{#graph:pie|size=350x200;title=Registered Molecules
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({{#count:{{#var:FLN}}}} total);legend=0.01x0.2;label=;
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FLNA={{#count:{{#choose:{{#var:FLN}}|FLNA}}}};
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FLNB={{#count:{{#choose:{{#var:FLN}}|FLNB}}}};
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FLNC={{#count:{{#choose:{{#var:FLN}}|FLNC}}}};
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FLND={{#count:{{#choose:{{#var:FLN}}|FLND}}}};
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FLNE={{#count:{{#choose:{{#var:FLN}}|FLNE}}}};
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FLNF={{#count:{{#choose:{{#var:FLN}}|FLNF}}}};
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}}
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{{#graph:pie|size=350x200;title=Metabolite-Species Data ({{#countLine:&&FLN|Reference}} total);legend=0.01x0.2;label=;
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FLNA={{#count:{{#choose:{{#var:rFLN}}|&&FLNA}}}};
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FLNB={{#count:{{#choose:{{#var:rFLN}}|&&FLNB}}}};
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FLNC={{#count:{{#choose:{{#var:rFLN}}|&&FLNC}}}};
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FLND={{#count:{{#choose:{{#var:rFLN}}|&&FLND}}}};
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FLNE={{#count:{{#choose:{{#var:rFLN}}|&&FLNE}}}};
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FLNF={{#count:{{#choose:{{#var:rFLN}}|&&FLNF}}}};
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}}
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{{FL_pie_chart|FLN}}
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[[Category:FL]]
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<!--- Class Information (Do not delete. It is used by Template:Hierarchy.)
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&&FLN&&Neoflavonoid&&
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&&FLNA&&4-Arylcoumarin&&
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&&FLNA1C&&7,3',4'-Trihydroxy-4-phenylcoumarin and O-methyl derivatives&&
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&&FLNA1CNS&&Simple substitution&&
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&&FLNA29&&6,7,(3'),(5')-Trihydroxy-4-phenylcoumarin and O-methyl derivatives&&
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&&FLNA29NS&&Simple substitution&&
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&&FLNA2A&&6,7,4'-Trihydroxy-4-phenylcoumarin and O-methyl derivatives&&
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&&FLNA2ANS&&Simple substitution&&
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&&FLNA2C&&6,7,3',4'-Tetrahydroxy-4-phenylcoumarin and O-methyl derivatives&&
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&&FLNA2CNS&&Simple substitution&&
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&&FLNA49&&6,7,8,(3'),(5')-Trihydroxy-4-phenylcoumarin and O-methyl derivatives&&
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&&FLNA49NS&&Simple substitution&&
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&&FLNAA9&&5,7,(3'),(5')-Trihydroxy-4-phenylcoumarin and O-methyl derivatives&&
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&&FLNAA9GS&&O-Glycoside&&
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&&FLNAA9NF&&Furanoflavonoid&&
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&&FLNAA9NI&&Non-cyclic prenyl substituted&&
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&&FLNAA9NP&&Pyranoflavonoid&&
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&&FLNAA9NS&&Simple substitution&&
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&&FLNAAB&&5,7-Dihydroxy-4'-methoxy-4-phenylcoumarin&&
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&&FLNAABNS&&Simple substitution&&
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&&FLNAAC&&5,7,3',4'-Tetrahydroxy-4-phenylcoumarin&&
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&&FLNAACGS&&O-Glycoside&&
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&&FLNAAL&&5,7,2',(3'),4',(5'),(6')-Hydroxy-4-phenylcoumarin&&
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&&FLNAALGS&&O-Glycoside&&
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&&FLNAALNM&&C-Methyl or C2/C3 substituted&&
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&&FLNABE&&7,3'-Dihydroxy-5,4'-dimethoxy-4-phenylcoumarin&&
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&&FLNABENM&&C-Methyl or C2/C3 substituted&&
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&&FLNABENS&&Simple substitution&&
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&&FLNACA&&5,4'-Dihydroxy-7-methoxy-4-phenylcoumarin&&
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&&FLNACAGS&&O-Glycoside&&
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&&FLNACB&&5-Hydroxy-7,4'-dimethoxy-4-phenylcoumarin&&
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&&FLNACBGS&&O-Glycoside&&
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&&FLNACC&&5,3',4'-Trihydroxy-7-methoxy-4-phenylcoumarin&&
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&&FLNACCGS&&O-Glycoside&&
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&&FLNACCNS&&Simple substitution&&
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&&FLNACE&&5,3'-Dihydroxy-7,4'-dimethoxy-4-phenylcoumarin&&
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&&FLNACENS&&Simple substitution&&
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&&FLNADA&&4'-Hydroxy-5,7-dimethoxy-4-phenylcoumarin&&
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&&FLNADANS&&Simple substitution&&
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&&FLNADB&&5,7,4'-Trimethoxy-4-phenylcoumarin&&
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&&FLNADBNS&&Simple substitution&&
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&&FLNADC&&3',4'-Dihydroxy-5,7-dimethoxy-4-phenylcoumarin&&
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&&FLNADCNS&&Simple substitution&&
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&&FLNADE&&3'-Hydroxy-5,7,4'-trimethoxy-4-phenylcoumarin&&
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&&FLNADENS&&Simple substitution&&
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&&FLNAFA&&5,7,8,4'-Tetrahydroxy-4-phenylcoumarin and O-methyl derivatives&&
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&&FLNAFANS&&Simple substitution&&
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&&FLNAFC&&5,7,8,3',4'-Pentahydroxy-4-phenylcoumarin and O-methyl derivatives&&
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&&FLNAFCNS&&Simple substitution&&
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&&FLNAQU&&4-Arylcoumarin quinone&&
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&&FLNAQUNI&&Non-cyclic prenyl substituted&&
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&&FLNARN&&5-O-2'-Cycled 4-aryocoumarin and O-methyl derivatives&&
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&&FLNARNNS&&Simple substitution&&
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&&FLNB&&4-Arylchroman&&
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&&FLNB2C&&Brazilin and O-methyl derivatives&&
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&&FLNB2CNS&&Simple substitution&&
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&&FLNB3C&&Haematoxylin and O-methyl derivatives&&
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&&FLNB3CNS&&Simple substitution&&
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&&FLNC&&Dalbergiquinol&&
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&&FLNC28&&2,4,5,2',(3'),(5'),(6')-Hydroxydalbergiquinol and O-methyl derivatives&&
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&&FLNC28NS&&Simple substitution&&
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&&FLNC29&&2,4,5,(3'),(5')-Hydroxydalbergiquinol and O-methyl derivatives&&
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&&FLNC29NS&&Simple substitution&&
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&&FLNC49&&2,3,4,5,(3'),(5')-Hydroxydalbergiquinol and O-methyl derivatives&&
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&&FLNC49NS&&Simple substitution&&
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&&FLNC4A&&2,3,4,5,4'-Pentahydroxydalbergiquinol and O-methyl derivatives&&
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&&FLNC4ANS&&Simple substitution&&
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&&FLND&&Dalbergione&&
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&&FLND29&&4,(3'),(5')-Hydroxydalbergione and O-methyl derivatives&&
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&&FLND29NS&&Simple substitution&&
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&&FLND2A&&4,4'-Hydroxydalbergione and O-methyl derivatives&&
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&&FLND2ANS&&Simple substitution&&
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&&FLND2C&&4,3',4'-Hydroxydalbergione and O-methyl derivatives&&
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&&FLND2CNS&&Simple substitution&&
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&&FLND49&&3,4,(3'),(5')-Hydroxydalbergione and O-methyl derivatives&&
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&&FLND49NS&&Simple substitution&&
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&&FLND4A&&3,4,4'-Hydroxydalbergione and O-methyl derivatives&&
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&&FLND4ANS&&Simple substitution&&
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&&FLNE&&Neoflavene&&
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&&FLNE29&&6,7,(3),(5)-Hydroxyneoflavene and O-methyl derivatives&&
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&&FLNE29NS&&Simple substitution&&
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&&FLNE49&&6,7,8,(3),(5)-Hydroxyneoflavene and O-methyl derivatives&&
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&&FLNE49NS&&Simple substitution&&
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&&FLNF&&Coumarinic acid&&
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&&FLNF19&&2,4,(3'),(5')-Hydroxycoumarinic acid&&
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&&FLNF19NP&&Pyranoflavonoid&&
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&&FLNFA9&&2,4,6,(3'),(5')-Hydroxycoumarinic acid&&
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&&FLNFA9NP&&Pyranoflavonoid&&
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--->

Revision as of 19:25, 24 May 2012

Neoflavonoid


Flavonoid Top Molecule Index Author Index Journals Structure Search Food New Input

Upper classes : FL Flavonoid

Overview

2nd Class
FLNA 4-Arylcoumarin
Flna.png 		FLNB 4-Arylchroman
Flnb.png 		FLNC Dalbergiquinol
Flnc.png
FLND Dalbergione
Flnd.png 		FLNE Neoflavene
Flne.png 		FLNF Coumarinic acid
Flnf.png

Database statistics

Major Plant Families

 The number in each family is counted as the number of genera (not species) listed in our registered references. Each reference record is accessible by clicking the link in compound pages. The taxonomy follows the APG-II classification. For details (or if the figure is broken), visit this page.

各科のカウントは種名でなく文献に記載された属名の数です。文献は代謝物ページのリンクからたどれ、分類はAPG-IIです。左の図が表示されない場合はここをクリックしてください。

Subcategories

This category has the following 6 subcategories, out of 6 total.

F

  • [×] FLNA‎ (empty)
  • [×] FLNB‎ (empty)
  • [×] FLNC‎ (empty)
  • [×] FLND‎ (empty)
  • [×] FLNE‎ (empty)
  • [×] FLNF‎ (empty)
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