Category:FL4D

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{{Huge|Dihydroflavonol}}
 
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{{Hierarchy|{{PAGENAME}}}}
  
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===Category description of FL4D: Dihydroflavonol===
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=={{Bilingual|ジヒドロフラボノールの概要|Overview}}==
  
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{| class="wikitable" border="1" cellpadding="2" cellspacing="1" style="font-size: smaller; float: center; clear: none; margin: 1em 1em 1em 1em"
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{{Twocolumn|
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In this database, we separate dihydroflavonols from the other flavonols mainly because of the abundance of flavonols.
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! ID
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Dihydroflavonol is widely distributed in ferns, gymnosperms and angiosperms.
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! Description
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Many aglycones occur in wood, bark, leaf resin or roots as free states.  C-glycosides are rare.
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! Note
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このデーターベースでは、フラボノールの数が非常に多いためジヒドロフラボノールを他と分けています。
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{{#repeat: PreTableRow3|1|
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ジヒドロフラボノールはシダから裸子植物、被子植物まで広くみられます。アグリコンの多くは木、皮、樹脂、根などに遊離しており、C-配糖体は稀です。
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<!---START OF ID & DESCRIPTION & NOTE --->
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}}
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&&FL4D19&&7,(3'),(5')-Hydroxydihydroflavonol and O-methyl derivatives&&
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{{FL_digit56|FL4D}}
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&&FL4D19NF&&Furanoflavonoid&&
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&&FL4D19NP&&Pyranoflavonoid&&
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&&FL4D19NS&&Simple substitution&&
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&&FL4D1A&&Garbanzol and O-methyl derivatives&&
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&&FL4D1AGS&&O-Glycoside&&
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&&FL4D1ANI&&Non-cyclic prenyl substituted&&
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&&FL4D1ANP&&Pyranoflavonoid&&
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&&FL4D1ANS&&Simple substitution&&
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&&FL4D1C&&Fustin and O-methyl derivatives&&
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&&FL4D1CGS&&O-Glycoside&&
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&&FL4D1CNS&&Simple substitution&&
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&&FL4D1G&&Dihydrorobinetin and O-methyl derivatives&&
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&&FL4D1GNS&&Simple substitution&&
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&&FL4D29&&6,7,(3'),(5')-Hydroxydihydroflavonol and O-methyl derivatives&&
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&&FL4D29NS&&Simple substitution&&
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&&FL4D3C&&8-Hydroxyfustin and O-methyl derivatives&&
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&&FL4D3CNS&&Simple substitution&&
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&&FL4DA8&&5,7,2',(3'),(5'),(6')-Hydroxydihydroflavonol and O-methyl derivatives&&
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&&FL4DA8GS&&O-Glycoside&&
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&&FL4DA8NP&&Pyranoflavonoid&&
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&&FL4DA8NS&&Simple substitution&&
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&&FL4DA9&&5,7,(3'),(5')-Hydroxydihydroflavonol and O-methyl derivatives&&
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&&FL4DA9GS&&O-Glycoside&&
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&&FL4DA9NI&&Non-cyclic prenyl substituted&&
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&&FL4DA9NM&&C-Methyl or C2/C3 substituted&&
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&&FL4DA9NN&&Flavonophenylpropanoid&&
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&&FL4DA9NP&&Pyranoflavonoid&&
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&&FL4DA9NS&&Simple substitution&&
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&&FL4DAA&&Dihydrokaempferol (Aromadendrin)&&
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&&FL4DAACS&&C-Glycoside&&
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&&FL4DAAGI&&Non-cyclic prenyl substituted flavonoid O-glycoside&&
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&&FL4DAAGM&&C-Methyl or C2/C3 substituted flavononoid O-glycoside&&
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&&FL4DAAGP&&Pyranoflavonoid O-glycoside&&
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&&FL4DAAGS&&O-Glycoside&&
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&&FL4DAANC&&Flavonoid substituted by complex substituent&&
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&&FL4DAANF&&Furanoflavonoid&&
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&&FL4DAANI&&Non-cyclic prenyl substituted&&
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&&FL4DAANP&&Pyranoflavonoid&&
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&&FL4DAANS&&Simple substitution&&
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&&FL4DAB&&Dihydrokaempferide&&
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&&FL4DABGS&&O-Glycoside&&
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&&FL4DABNM&&C-Methyl or C2/C3 substituted&&
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&&FL4DABNS&&Simple substitution&&
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&&FL4DAC&&Dihydroquercetin (Taxifolin)&&
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&&FL4DACCS&&C-Glycoside&&
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&&FL4DACGI&&Non-cyclic prenyl substituted flavonoid O-glycoside&&
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&&FL4DACGS&&O-Glycoside&&
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&&FL4DACNC&&Flavonoid substituted by complex substituent&&
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&&FL4DACNI&&Non-cyclic prenyl substituted&&
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&&FL4DACNM&&C-Methyl or C2/C3 substituted&&
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&&FL4DACNN&&Flavonophenylpropanoid&&
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&&FL4DACNR&&Ring containing prenyl substituted&&
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&&FL4DACNS&&Simple substitution&&
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&&FL4DAD&&Dihydroisorhamnetin&&
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&&FL4DADNI&&Non-cyclic prenyl substituted&&
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&&FL4DADNP&&Pyranoflavonoid&&
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&&FL4DADNS&&Simple substitution&&
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&&FL4DAE&&Dihydroquercetin 4'-methyl ether (Taxifolin 4'-methyl ether)&&
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&&FL4DAEGS&&O-Glycoside&&
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&&FL4DAENI&&Non-cyclic prenyl substituted&&
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&&FL4DAENS&&Simple substitution&&
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&&FL4DAG&&Dihydromyricetin (Ampelopsin)&&
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&&FL4DAGGM&&C-Methyl or C2/C3 substituted flavononoid O-glycoside&&
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&&FL4DAGGS&&O-Glycoside&&
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&&FL4DAGNM&&C-Methyl or C2/C3 substituted&&
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&&FL4DAGNS&&Simple substitution&&
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&&FL4DAGNS0&&Normal&&
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&&FL4DAGNSS&&Sulfate incluted&&
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&&FL4DAH&&Dihydromyricetin 3'-methyl ether (Ampelopsin 3'-methyl ether)&&
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&&FL4DAHGS&&O-Glycoside&&
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&&FL4DAHNS&&Simple substitution&&
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&&FL4DAI&&Dihydrosyringetin&&
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&&FL4DAINS&&Simple substitution&&
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&&FL4DAJ&&Pallasiin&&
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&&FL4DAJNS&&Simple substitution&&
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&&FL4DAL&&5,7,2',(3'),4',(5'),(6')-Hydroxydihydroflavonol and O-methyl derivatives&&
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&&FL4DALNF&&Furanoflavonoid&&
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&&FL4DALNI&&Non-cyclic prenyl substituted&&
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&&FL4DALNP&&Pyranoflavonoid&&
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&&FL4DALNS&&Simple substitution&&
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&&FL4DBA&&Dihydrokaempferol 5-methyl ether (Aromadendrin 5-methyl ether)&&
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&&FL4DBANI&&Non-cyclic prenyl substituted&&
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&&FL4DBANM&&C-Methyl or C2/C3 substituted&&
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&&FL4DBANP&&Pyranoflavonoid&&
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&&FL4DBANS&&Simple substitution&&
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&&FL4DBC&&Dihydroquercetin 5-methyl ether (Taxifolin 5-methyl ether)&&
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&&FL4DBCGS&&O-Glycoside&&
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&&FL4DBCNS&&Simple substitution&&
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&&FL4DCA&&Dihydrokaempferol 7-methyl ether (Aromadendrin 7-methyl ether)&&
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&&FL4DCACS&&C-Glycoside&&
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&&FL4DCAGS&&O-Glycoside&&
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&&FL4DCANS&&Simple substitution&&
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&&FL4DCB&&Dihydrokaempferol 7,4'-dimethyl ether (Aromadendrin 7,4'-dimethyl ether)&&
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&&FL4DCBGS&&O-Glycoside&&
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&&FL4DCBNC&&Flavonoid substituted by complex substituent&&
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&&FL4DCBNS&&Simple substitution&&
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&&FL4DCC&&Padmatin and Epipadmatin&&
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&&FL4DCCGS&&O-Glycoside&&
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&&FL4DCCNS&&Simple substitution&&
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&&FL4DCD&&Taxifolin 7,3'-dimethyl ether&&
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&&FL4DCDNI&&Non-cyclic prenyl substituted&&
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&&FL4DCDNS&&Simple substitution&&
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&&FL4DCE&&Taxifolin 7,4'-dimethyl ether&&
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&&FL4DCENI&&Non-cyclic prenyl substituted&&
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&&FL4DCENS&&Simple substitution&&
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&&FL4DDA&&Aromadendrin O-methyl derivatives (4'-hydroxy, without FL4DBA, FL4DCA)&&
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&&FL4DDANP&&Pyranoflavonoid&&
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&&FL4DDANS&&Simple substitution&&
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&&FL4DDB&&Aromadendrin O-methul derivatives (4'-methoxy, without FL4DAB, FL4DBB, FL4DCB)&&
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&&FL4DDBNS&&Simple substitution&&
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&&FL4DDC&&Taxiforin O-methyl derivatives (3',4'-hydroxy, without FL4DBC, FL4DCC)&&
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&&FL4DDCNS&&Simple substitution&&
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&&FL4DE8&&5,6,7,2',(3'),(5'),(6')-Hydroxydihydroflavonol and O-methyl derivatives&&
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&&FL4DE8NI&&Non-cyclic prenyl substituted&&
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&&FL4DE8NS&&Simple substitution&&
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&&FL4DE9&&5,6,7,(3'),(5')-Hydroxydihydroflavonol and O-methyl derivatives&&
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&&FL4DE9NF&&Furanoflavonoid&&
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&&FL4DE9NS&&Simple substitution&&
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&&FL4DEA&&6-Hydroxyaromadendrin and O-methyl derivatives&&
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&&FL4DEANS&&Simple substitution&&
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&&FL4DEC&&6-Hydroxytaxiforin and O-methyl derivaitves&&
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&&FL4DECNF&&Furanoflavonoid&&
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&&FL4DECNS&&Simple substitution&&
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&&FL4DF8&&5,7,8,2',(3'),(5'),(6')-Hydroxydihydroflavonol and O-methyl derivatives&&
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&&FL4DF8NS&&Simple substitution&&
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&&FL4DF9&&5,7,8,(3'),(5')-Hydroxydihydroflavonol and O-methyl derivatives&&
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&&FL4DF9NI&&Non-cyclic prenyl substituted&&
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&&FL4DF9NS&&Simple substitution&&
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&&FL4DFA&&8-Hydroxyaromadendrin and O-methyl derivatives&&
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&&FL4DFAGS&&O-Glycoside&&
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&&FL4DFANI&&Non-cyclic prenyl substituted&&
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&&FL4DFANS&&Simple substitution&&
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&&FL4DFC&&Dihydrogossypetin and O-methyl derivatives&&
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&&FL4DFCNS&&Simple substitution&&
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&&FL4DG9&&5,6,7,8,(3'),(5')-Hydroxydihydroflavonol and O-methyl derivatives&&
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&&FL4DG9NS&&Simple substitution&&
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&&FL4DPT&&Peltogynoid dihydroflavonol&&
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&&FL4DPTNS&&Simple substitution&&
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&&FL4DQU&&Dihydroflavonol quinone&&
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&&FL4DQUNN&&Flavonophenylpropanoid&&
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&&FL4DQUNP&&Pyranoflavonoid&&
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&&FL4DRN&&3-O-2' Cycled dihydroflavonol&&
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&&FL4DRNNI&&Non-cyclic prenyl substituted&&
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&&FL4DRNNP&&Pyranoflavonoid&&
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&&FL4DRNNR&&Ring containing prenyl substituted&&
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<!---END OF ID & DESCRIPTION & NOTE --->
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|\n|1=}}
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|}
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Latest revision as of 17:30, 18 August 2010

Dihydroflavonol


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

Upper classes : FL Flavonoid : FL4 Dihydroflavonol

Contents

[edit] Overview

In this database, we separate dihydroflavonols from the other flavonols mainly because of the abundance of flavonols. Dihydroflavonol is widely distributed in ferns, gymnosperms and angiosperms. Many aglycones occur in wood, bark, leaf resin or roots as free states. C-glycosides are rare.

Fl4d.png


[edit] 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。

[edit] Patterns of Hydroxylation

The 5th and 6th digits of our flavonoid ID indicates the hydroxylation patterns of A-ring and B-ring (See the upper-right figure. The leftmost ring is A, rightmost is B), respectively. The following chart is spanned by these 2 digits. R indicates H or CH3, and R' indicates H or R. Numbers are IUPAC positions. The value in each cell (such as GS: glycosilation only) corresponds to the 7th and 8th digits, which is explained at the bottom of this page.


Details of the 3rd Class: Hydroxylation pattern of A and B rings (5th and 6th digits)

Position of -OH (-OCH3) groups
      6th digit →
5th digit ↓

FL A.png FL B.png FL C.png FL D.png FL E.png FL F.png FL G.png FL H.png FL I.png FL J.png FL K.png FL L.png FL 8.png FL 9.png
 A (74 pages)  B (11 pages)  C (72 pages)  D (7 pages)  E (7 pages)  F (0 pages)  G (11 pages)  H (3 pages)  I (1 pages)  J (1 pages)  K (0 pages)  L (16 pages)  8 (15 pages)  9 (37 pages)
FL A .png  A (169 pages)  CS (2 pages) GI (4 pages) GM (1 pages) GP (1 pages) GS (12 pages) NC (5 pages) NF (2 pages) NI (10 pages) NP (3 pages) NS (2 pages)  GS (2 pages) NM (1 pages) NS (2 pages)  CS (1 pages) GI (1 pages) GS (31 pages) NC (3 pages) NI (4 pages) NM (3 pages) NN (4 pages) NR (1 pages) NS (2 pages)  NI (1 pages) NP (1 pages) NS (1 pages)  GS (1 pages) NI (1 pages) NS (1 pages)  GM (1 pages) GS (3 pages) NM (2 pages) NS (3 pages)  GS (1 pages) NS (2 pages)  NS (1 pages)  NS (1 pages)  NF (2 pages) NI (12 pages) NP (1 pages) NS (1 pages)  GS (1 pages) NP (2 pages) NS (7 pages)  GS (4 pages) NI (5 pages) NM (2 pages) NN (1 pages) NP (2 pages) NS (12 pages)
FL B .png  B (7 pages)  NI (2 pages) NM (1 pages) NP (1 pages) NS (1 pages)  GS (1 pages) NS (1 pages)
FL C .png  C (24 pages)  CS (1 pages) GS (2 pages) NS (3 pages)  GS (2 pages) NC (2 pages) NS (1 pages)  GS (2 pages) NS (3 pages)  NI (2 pages) NS (2 pages)  NI (2 pages) NS (2 pages)
FL D .png  D (6 pages)  NP (1 pages) NS (3 pages)  NS (1 pages)  NS (1 pages)
FL E .png  E (12 pages)  NS (4 pages)  NF (1 pages) NS (1 pages)  NI (1 pages) NS (1 pages)  NF (1 pages) NS (3 pages)
FL F .png  F (14 pages)  GS (3 pages) NI (1 pages) NS (3 pages)  NS (2 pages)  NS (3 pages)  NI (1 pages) NS (1 pages)
FL G .png  G (1 pages)  NS (1 pages)
FL 1 .png  1 (18 pages)  GS (2 pages) NI (2 pages) NP (1 pages) NS (1 pages)  GS (3 pages) NS (4 pages)  NS (2 pages)  NF (1 pages) NP (1 pages) NS (1 pages)
FL 2 .png  2 (1 pages)  NS (1 pages)
FL 3 .png  3 (3 pages)  NS (3 pages)
FL 4 .png  4 (0 pages)
FL 9 .png  9 (0 pages)

Abbreviations used in the above chart

First Characters 

N not glycosylated; G O-glycoside; C C-glycoside; D both glycosides;

Second Characters 

S not modified; M alkylated; I prenylated; R cyclic-prenylated; F furanoFL; P pyranoFL; D furano and pyranoFL; N phenylpropanoid; C others;

Special Second Character only for Anthycyanin (FL7) 

A Galactosylated; L Glucosylated; O modified with other sugars;

[edit] Other Unusual Patterns

These types are not classified in the above chart.

Quinone  QU (2 pages) alpha-Hydroxy  HX (0 pages) beta-Hydroxy  HY (0 pages) Peltogynoid  PT (5 pages)
Retrocalchone  RT (0 pages) Dehydro-backbone  WX (0 pages) Additional rings  RN (10 pages) Others  UN (0 pages)
Pyranoanthocyanin (FL7 only)  RX (0 pages)

[edit] Patterns of Glycosylation

The 7th and 8th digits of the flavonoid ID indicates the glycosylation, and other modification patterns, respectively. The following chart is spanned by these 2 digits. The value in each cell (such as AA for the standard form) corresponds to the 5th and 6th digits.


Details of the 4th Class: Glycosylation patterns (7th and 8th digits)
      7th digit →
8th digit ↓ 		No glycosylation  N (190 pages) O-glycoside  G (78 pages) C-glycoside  C (4 pages) O- & C-glycoside  D (0 pages)
no modification  S (163 pages)  19 (1 pages) 1A (1 pages) 1C (4 pages) 1G (2 pages) 29 (1 pages) 3C (3 pages) A8 (7 pages) A9 (12 pages) AA (2 pages) AB (2 pages) AC (2 pages) AD (1 pages) AE (1 pages) AG (3 pages) AH (2 pages) AI (1 pages) AJ (1 pages) AL (1 pages) BA (1 pages) BC (1 pages) CA (3 pages) CB (1 pages) CC (3 pages) CD (2 pages) CE (2 pages) DA (3 pages) DB (1 pages) DC (1 pages) E8 (1 pages) E9 (3 pages) EA (4 pages) EC (1 pages) F8 (3 pages) F9 (1 pages) FA (3 pages) FC (2 pages) G9 (1 pages) PT (5 pages)  1A (2 pages) 1C (3 pages) A8 (1 pages) A9 (4 pages) AA (12 pages) AB (2 pages) AC (31 pages) AE (1 pages) AG (3 pages) AH (1 pages) BC (1 pages) CA (2 pages) CB (2 pages) CC (2 pages) FA (3 pages)  AA (2 pages) AC (1 pages) CA (1 pages)
alkylated  M (11 pages)  A9 (2 pages) AB (1 pages) AC (3 pages) AG (2 pages) BA (1 pages)  AA (1 pages) AG (1 pages)
prenylated  I (0 pages)  1A (2 pages) A9 (5 pages) AA (10 pages) AC (4 pages) AD (1 pages) AE (1 pages) AL (12 pages) BA (2 pages) CD (2 pages) CE (2 pages) E8 (1 pages) F9 (1 pages) FA (1 pages) RN (5 pages)  AA (4 pages) AC (1 pages)
cyclic prenylated  R (0 pages)  AC (1 pages) RN (1 pages)
furano FL  F (7 pages)  19 (1 pages) AA (2 pages) AL (2 pages) E9 (1 pages) EC (1 pages)
pyrano FL  P (19 pages)  19 (1 pages) 1A (1 pages) A8 (2 pages) A9 (2 pages) AA (3 pages) AD (1 pages) AL (1 pages) BA (1 pages) DA (1 pages) QU (1 pages) RN (4 pages)  AA (1 pages)
furano & pyrano FL  D (0 pages)
prenylpropanoid  N (6 pages)  A9 (1 pages) AC (4 pages) QU (1 pages)
others  C (10 pages)  AA (5 pages) AC (3 pages) CB (2 pages)
3-Gal related A N.A. N.A. N.A.
3-Glc related L N.A. N.A. N.A.
other sugar at 3 O N.A. N.A. N.A.

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