Category:FL2F

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{{Huge|Flavanone}}
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{{Hierarchy|{{PAGENAME}}}}
 
{{Hierarchy|{{PAGENAME}}}}
  
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===Category description of FL2F: Flavanone===
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=={{Bilingual|フラバノンの概要|Overview}}==
 +
 
 +
{{Twocolumn|
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Not only [[:Category:Asteraceae|Asteraceae]] and [[:Category:Fabaceae|Fabaceae]] but also [[:Category:Lamiaceae|Lamiaceae]] and [[:Category:Rutaceae|Rutaceae]] contain many flavanones. Aglycones occur as free state in bark, roots and root barks. In ferns, aglycones exist as farinose exudates of fronds.
 +
Two flavanone glycosides were also isolated from a liverwort [[Species:Riccia|Riccia]].
 +
 
 +
[[FL2F1CGS0001|Butrin]], glucoside of [[FL2F1CNS0001|Butin]], was the first flavanone identified in nature by [[Reference:Lal_JB:Dutt_S:%2CJ._Indian_Chem._Soc.%2C1935%2C12%2C262|Lal and Dutt (1935)]].
 +
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フラバノンは[[:Category:Asteraceae|キク科]]や[[:Category:Fabaceae|マメ科]]だけでなく[[:Category:Lamiaceae|シソ科]]や[[:Category:Rutaceae|ミカン科]]にも豊富です。アグリコンは皮や根、根の皮部分に多く含まれます。シダ類では葉状体の白い粉ふき様に存在します。フラバノンはゼニゴケ類[[Species:Riccia|Riccia]]からも見つかります。
 +
 
 +
一番最初に同定されたフラバノンは、[[FL2F1CNS0001|ブチン]]の配糖体である[[FL2F1CGS0001|ブトリン]]です([[Reference:Lal_JB:Dutt_S:%2CJ._Indian_Chem._Soc.%2C1935%2C12%2C262|Lal and Dutt, 1935]])。
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}}
  
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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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{{FL_digit56|FL2F}}
−
|-
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−
! ID
+
−
! Description
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! Note
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−
|-
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{{#repeat: PreTableRow3|1|
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<!---START OF ID & DESCRIPTION & NOTE --->
+
−
&&FL2F18&&7,2',(3'),(5')-Hydroxyflavanone and O-methyl derivatives&&
+
−
&&FL2F18NC&&Flavonoid substituted by complex substituent&&
+
−
&&FL2F19&&7,(3'),(5')-Hydroxyflavanone and O-methyl derivatives&&
+
−
&&FL2F19GM&&C-Methyl or C2/C3 substituted flavononoid O-glycoside&&
+
−
&&FL2F19GS&&O-Glycoside&&
+
−
&&FL2F19NC&&Flavonoid substituted by complex substituent&&
+
−
&&FL2F19NI&&Non-cyclic prenyl substituted&&
+
−
&&FL2F19NP&&Pyranoflavonoid&&
+
−
&&FL2F19NS&&Simple substitution&&
+
−
&&FL2F1A&&Liquiritigenin and O-methyl derivatives&&
+
−
&&FL2F1ACS&&C-Glycoside&&
+
−
&&FL2F1AGS&&O-Glycoside&&
+
−
&&FL2F1AGS0&&Normal&&
+
−
&&FL2F1AGSN&&Nitrogen incluted&&
+
−
&&FL2F1ANF&&Furanoflavonoid&&
+
−
&&FL2F1ANI&&Non-cyclic prenyl substituted&&
+
−
&&FL2F1ANM&&C-Methyl or C2/C3 substituted&&
+
−
&&FL2F1ANN&&Flavonophenylpropanoid&&
+
−
&&FL2F1ANP&&Pyranoflavonoid&&
+
−
&&FL2F1ANS&&Simple substitution&&
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−
&&FL2F1C&&Butin and O-methyl derivatives&&
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−
&&FL2F1CCS&&C-Glycoside&&
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−
&&FL2F1CGS&&O-Glycoside&&
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−
&&FL2F1CNF&&Furanoflavonoid&&
+
−
&&FL2F1CNI&&Non-cyclic prenyl substituted&&
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−
&&FL2F1CNP&&Pyranoflavonoid&&
+
−
&&FL2F1CNS&&Simple substitution&&
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−
&&FL2F1L&&7,2',(3'),4',(5'),(6')-Hydroxyflavanone and O-methyl derivatives&&
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−
&&FL2F1LNF&&Furanoflavonoid&&
+
−
&&FL2F1LNI&&Non-cyclic prenyl substituted&&
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−
&&FL2F1LNS&&Simple substitution&&
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−
&&FL2F29&&6,7,(3'),(5')-Hydroxyflavanone and O-methyl derivatives&&
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−
&&FL2F29NF&&Furanoflavonoid&&
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−
&&FL2F29NP&&Pyranoflavonoid&&
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−
&&FL2F2C&&Plathymenin and O-methyl derivatives&&
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−
&&FL2F2CNI&&Non-cyclic prenyl substituted&&
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−
&&FL2F2CNP&&Pyranoflavonoid&&
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−
&&FL2F2CNS&&Simple substitution&&
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&&FL2F39&&7,8,(3'),(5')-Hydroxyflavanone and O-methyl derivatives&&
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−
&&FL2F39NS&&Simple substitution&&
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−
&&FL2F3A&&7,8,4'-Trihydroxyflavanone and O-methyl derivatives&&
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&&FL2F3ANS&&Simple substitution&&
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&&FL2F3C&&Isookanin and O-methyl derivatives&&
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−
&&FL2F3CGS&&O-Glycoside&&
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−
&&FL2F3CNS&&Simple substitution&&
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−
&&FL2F3G&&7,8,3',4',5'-Pentahydroxyflavanone O-methyl derivatives&&
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&&FL2F3GGS&&O-Glycoside&&
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−
&&FL2F4A&&6,7,8,4'-Tetrahydroxyflavanone&&
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&&FL2F4ANS&&Simple substitution&&
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&&FL2F99&&7,2',4'-Desoxyflavanone and O-methyl derivatives&&
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&&FL2F99NI&&Non-cyclic prenyl substituted&&
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&&FL2F9A&&7-Desoxyflavanone (4'-Hydroxy) and O-methyl derivatives&&
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&&FL2F9AGI&&Non-cyclic prenyl substituted flavonoid O-glycoside&&
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&&FL2F9ANI&&Non-cyclic prenyl substituted&&
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&&FL2F9ANS&&Simple substitution&&
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&&FL2F9C&&7-Desoxyflavanone (3',4'-Hydroxy) and O-methyl derivatives&&
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&&FL2F9CNS&&Simple substitution&&
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−
&&FL2FA8&&5,7,2',(3'),(5'),(6')-Hydroxyflavanone and O-methyl derivatives&&
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−
&&FL2FA8GS&&O-Glycoside&&
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−
&&FL2FA8NI&&Non-cyclic prenyl substituted&&
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−
&&FL2FA8NP&&Pyranoflavonoid&&
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−
&&FL2FA8NS&&Simple substitution&&
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−
&&FL2FA9&&5,7,(3'),(5')-Hydroxyflavanone and O-methyl derivatives&&
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−
&&FL2FA9GM&&C-Methyl or C2/C3 substituted flavononoid O-glycoside&&
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−
&&FL2FA9GS&&O-Glycoside&&
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−
&&FL2FA9NC&&Flavonoid substituted by complex substituent&&
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&&FL2FA9NF&&Furanoflavonoid&&
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&&FL2FA9NI&&Non-cyclic prenyl substituted&&
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&&FL2FA9NM&&C-Methyl or C2/C3 substituted&&
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&&FL2FA9NN&&Flavonophenylpropanoid&&
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&&FL2FA9NP&&Pyranoflavonoid&&
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&&FL2FA9NR&&Ring containing prenyl substituted&&
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&&FL2FA9NS&&Simple substitution&&
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&&FL2FAA&&Naringenin&&
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&&FL2FAACS&&C-Glycoside&&
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&&FL2FAAGC&&Flavonoid O-glycoside substituted by complex substituent&&
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&&FL2FAAGI&&Non-cyclic prenyl substituted flavonoid O-glycoside&&
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&&FL2FAAGM&&C-Methyl or C2/C3 substituted flavononoid O-glycoside&&
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&&FL2FAAGS&&O-Glycoside&&
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&&FL2FAANF&&Furanoflavonoid&&
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−
&&FL2FAANI&&Non-cyclic prenyl substituted&&
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&&FL2FAANM&&C-Methyl or C2/C3 substituted&&
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&&FL2FAANM0&&Normal&&
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&&FL2FAANMH&&Halogen included&&
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&&FL2FAANN&&Flavonophenylpropanoid&&
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−
&&FL2FAANP&&Pyranoflavonoid&&
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−
&&FL2FAANS&&Simple substitution&&
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−
&&FL2FAANS0&&Normal&&
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−
&&FL2FAANSS&&Sulfate incluted&&
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&&FL2FAB&&Isosakuranetin&&
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−
&&FL2FABGM&&C-Methyl or C2/C3 substituted flavononoid O-glycoside&&
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−
&&FL2FABGS&&O-Glycoside&&
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−
&&FL2FABNI&&Non-cyclic prenyl substituted&&
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−
&&FL2FABNM&&C-Methyl or C2/C3 substituted&&
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−
&&FL2FABNN&&Flavonophenylpropanoid&&
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&&FL2FABNP&&Pyranoflavonoid&&
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−
&&FL2FABNS&&Simple substitution&&
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−
&&FL2FAC&&Eriodictyol&&
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−
&&FL2FACCS&&C-Glycoside&&
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−
&&FL2FACGM&&C-Methyl or C2/C3 substituted flavononoid O-glycoside&&
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−
&&FL2FACGS&&O-Glycoside&&
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−
&&FL2FACNF&&Furanoflavonoid&&
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−
&&FL2FACNI&&Non-cyclic prenyl substituted&&
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&&FL2FACNM&&C-Methyl or C2/C3 substituted&&
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&&FL2FACNN&&Flavonophenylpropanoid&&
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&&FL2FACNP&&Pyranoflavonoid&&
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&&FL2FACNS&&Simple substitution&&
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&&FL2FAD&&Homoeriodictyol&&
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−
&&FL2FADCS&&C-Glycoside&&
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−
&&FL2FADGS&&O-Glycoside&&
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−
&&FL2FADNI&&Non-cyclic prenyl substituted&&
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−
&&FL2FADNM&&C-Methyl or C2/C3 substituted&&
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−
&&FL2FADNP&&Pyranoflavonoid&&
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&&FL2FADNS&&Simple substitution&&
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&&FL2FAE&&Hesperetin&&
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&&FL2FAEGS&&O-Glycoside&&
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&&FL2FAENI&&Non-cyclic prenyl substituted&&
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&&FL2FAENP&&Pyranoflavonoid&&
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&&FL2FAENS&&Simple substitution&&
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&&FL2FAF&&Eriodictyol 3',4'-dimethyl ether&&
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&&FL2FAFGS&&O-Glycoside&&
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&&FL2FAFNI&&Non-cyclic prenyl substituted&&
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&&FL2FAG&&Dihydrotricetin&&
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−
&&FL2FAGGS&&O-Glycoside&&
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−
&&FL2FAGNS&&Simple substitution&&
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&&FL2FAI&&Dihydrotricetin 3',5'-dimethyl ether&&
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&&FL2FAIGS&&O-Glycoside&&
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−
&&FL2FAK&&5,7,5'-Trihydroxy-3',4'-dimethoxyflavanone&&
+
−
&&FL2FAKNM&&C-Methyl or C2/C3 substituted&&
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−
&&FL2FAL&&5,7,2',(3'),4',(5'),(6')-Hydroxyflavanone and O-methyl derivatives&&
+
−
&&FL2FALGS&&O-Glycoside&&
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−
&&FL2FALNI&&Non-cyclic prenyl substituted&&
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−
&&FL2FALNM&&C-Methyl or C2/C3 substituted flavononoid&&
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&&FL2FALNP&&Pyranoflavonoid&&
+
−
&&FL2FALNR&&Ring containing prenyl substituted&&
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−
&&FL2FALNS&&Simple substitution&&
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&&FL2FBA&&Naringenin 5-methyl ether&&
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−
&&FL2FBAGS&&O-Glycoside&&
+
−
&&FL2FBANC&&Flavonoid substituted by complex substituent&&
+
−
&&FL2FBANI&&Non-cyclic prenyl substituted&&
+
−
&&FL2FBANS&&Simple substitution&&
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−
&&FL2FBB&&Tsugafolin&&
+
−
&&FL2FBBNP&&Pyranoflavonoid&&
+
−
&&FL2FBBNS&&Simple substitution&&
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−
&&FL2FBC&&Eriodictyol 5-methyl ether&&
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−
&&FL2FBCGM&&C-Methyl or C2/C3 substituted flavononoid O-glycoside&&
+
−
&&FL2FBCGS&&O-Glycoside&&
+
−
&&FL2FBCNP&&Pyranoflavonoid&&
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&&FL2FBE&&Eriodictyol 5,4'-dimethyl ether&&
+
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&&FL2FBEGS&&O-Glycoside&&
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&&FL2FBF&&Eriodictyol 5,3',4'-trimethyl ether&&
+
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&&FL2FBFNP&&Pyranoflavonoid&&
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&&FL2FCA&&Sakuranetin&&
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&&FL2FCAGS&&O-Glycoside&&
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−
&&FL2FCANI&&Non-cyclic prenyl substituted&&
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&&FL2FCANM&&C-Methyl or C2/C3 substituted&&
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&&FL2FCANS&&Simple substitution&&
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&&FL2FCB&&Naringenin 7,4'-dimethyl ether&&
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&&FL2FCBGM&&C-Methyl or C2/C3 substituted flavononoid O-glycoside&&
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&&FL2FCBNI&&Non-cyclic prenyl substituted&&
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&&FL2FCBNS&&Simple substitution&&
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&&FL2FCC&&Sternbin&&
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&&FL2FCCGS&&O-Glycoside&&
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−
&&FL2FCCNF&&Furanoflavonoid&&
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&&FL2FCCNI&&Non-cyclic prenyl substituted&&
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&&FL2FCCNS&&Simple substitution&&
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&&FL2FCD&&Eriodictyol 7,3'-dimethyl ether&&
+
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&&FL2FCDGS&&O-Glycoside&&
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−
&&FL2FCDNI&&Non-cyclic prenyl substituted&&
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−
&&FL2FCDNS&&Simple substitution&&
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−
&&FL2FCE&&Persicogenin&&
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&&FL2FCEGS&&O-Glycoside&&
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&&FL2FCENS&&Simple substitution&&
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&&FL2FCF&&Eriodictyol 7,3',4'-trimethyl ether&&
+
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&&FL2FCFNM&&C-Methyl or C2/C3 substituted&&
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&&FL2FCFNS&&Simple substitution&&
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&&FL2FCH&&Dihydrotricetin 7,3'-dimethyl ether&&
+
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&&FL2FCHNS&&Simple substitution&&
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&&FL2FCK&&Dihydrotricetin O-methyl derivatives (5-Hydroxy-7-methoxy, without FL2FCH)&&
+
−
&&FL2FCKNS&&Simple substitution&&
+
−
&&FL2FDA&&Naringenin 5,7-dimethyl ether&&
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&&FL2FDAGS&&O-Glycoside&&
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−
&&FL2FDANS&&Simple substitution&&
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−
&&FL2FDB&&Naringenin trimethyl ether&&
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−
&&FL2FDBNS&&Simple substitution&&
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&&FL2FDC&&5,7-Dimethoxy-3',4'-hydroxyflavanone&&
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&&FL2FDCNS&&Simple substitution&&
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&&FL2FDE&&Eriodictyol 5,7,4'-trimethyl ether&&
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&&FL2FDENM&&C-Methyl or C2/C3 substituted&&
+
−
&&FL2FE8&&5,6,7,2',(3'),(5'),(6')-Hydroxyflavanone and O-methyl derivatives&&
+
−
&&FL2FE8NS&&Simple substitution&&
+
−
&&FL2FE9&&5,6,7,(3'),(5')-Hydroxyflavanone and O-methyl derivatives&&
+
−
&&FL2FE9GS&&O-Glycoside&&
+
−
&&FL2FE9NF&&Furanoflavonoid&&
+
−
&&FL2FE9NI&&Non-cyclic prenyl substituted&&
+
−
&&FL2FE9NS&&Simple substitution&&
+
−
&&FL2FEA&&Carthamidin and O-methyl derivatives&&
+
−
&&FL2FEAGI&&Non-cyclic prenyl substituted flavonoid O-glycoside&&
+
−
&&FL2FEAGS&&O-Glycoside&&
+
−
&&FL2FEANS&&Simple substitution&&
+
−
&&FL2FEC&&6-Hydroxyeriodictol and O-methyl derivatives&&
+
−
&&FL2FECNF&&Furanoflavonoid&&
+
−
&&FL2FECNS&&Simple substitution&&
+
−
&&FL2FEG&&5,6,7,3',4',5'-Hexahydroxyflavanone and O-methyl derivatives&&
+
−
&&FL2FEGGS&&O-Glycoside&&
+
−
&&FL2FEGNS&&Simple substitution&&
+
−
&&FL2FEL&&5,6,7,2',(3'),4',(5'),(6')-Hydroxyflavanone and O-methyl derivatives&&
+
−
&&FL2FELNS&&Simple substitution&&
+
−
&&FL2FF8&&5,7,8,2',(3'),(5'),(6')-Hydroxyflavanone and O-methyl derivatives&&
+
−
&&FL2FF8GS&&O-Glycoside&&
+
−
&&FL2FF8NI&&Non-cyclic prenyl substituted&&
+
−
&&FL2FF8NS&&Simple substitution&&
+
−
&&FL2FF9&&5,7,8,(3'),(5')-Hydroxyflavanone and O-methyl derivatives&&
+
−
&&FL2FF9GS&&O-Glycoside&&
+
−
&&FL2FF9NC&&Flavonoid substituted by complex substituent&&
+
−
&&FL2FF9NI&&Non-cyclic prenyl substituted&&
+
−
&&FL2FF9NS&&Simple substitution&&
+
−
&&FL2FFA&&5,7,8,4'-Tetrahydroxychalcone and O-methyl derivatives&&
+
−
&&FL2FFAGS&&O-Glycoside&&
+
−
&&FL2FFANI&&Non-cyclic prenyl substituted&&
+
−
&&FL2FFANS&&Simple substitution&&
+
−
&&FL2FFC&&8-Hydroxyeriodictol and O-methyl derivatives&&
+
−
&&FL2FFCNS&&Simple substitution&&
+
−
&&FL2FG8&&5,6,7,8,2',(3'),(5'),(6')-Hydroxyflavanone and O-methyl derivatives&&
+
−
&&FL2FG8NS&&Simple substitution&&
+
−
&&FL2FG9&&5,6,7,8,(3'),(5')-Hydroxyflavanone and O-methyl derivatives&&
+
−
&&FL2FG9NS&&Simple substitution&&
+
−
&&FL2FGA&&5,6,7,8,4'-Pentahydroxyflavanone&&
+
−
&&FL2FGANS&&Simple substitution&&
+
−
&&FL2FGG&&5,6,7,8,3',4',5'-Heptahydroxyflavanone and O-methyl derivatives&&
+
−
&&FL2FGGNS&&Simple substitution&&
+
−
&&FL2FHY&&2-Hydroxyflavanone&&
+
−
&&FL2FHYGS&&O-Glycoside&&
+
−
&&FL2FHYNM&&C-Methyl or C2/C3 substituted flavononoid&&
+
−
&&FL2FHYNS&&Simple substitution&&
+
−
&&FL2FQU&&Flavanone quinone&&
+
−
&&FL2FQUNM&&C-Methyl or C2/C3 substituted&&
+
−
&&FL2FQUNN&&Flavonophenylpropanoid&&
+
−
&&FL2FQUNR&&Ring containing prenyl substituted&&
+
−
&&FL2FQUNS&&Simple substitution&&
+
−
<!---END OF ID & DESCRIPTION & NOTE --->
+
−
|\n|1=}}
+
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|}
+

Latest revision as of 17:24, 18 August 2010

Flavanone


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

Upper classes : FL Flavonoid : FL2 Flavanone

Contents

[edit] Overview

Not only Asteraceae and Fabaceae but also Lamiaceae and Rutaceae contain many flavanones. Aglycones occur as free state in bark, roots and root barks. In ferns, aglycones exist as farinose exudates of fronds. Two flavanone glycosides were also isolated from a liverwort Riccia. Butrin, glucoside of Butin, was the first flavanone identified in nature by Lal and Dutt (1935).

Fl2f.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 (209 pages)  B (34 pages)  C (120 pages)  D (23 pages)  E (17 pages)  F (6 pages)  G (11 pages)  H (1 pages)  I (2 pages)  J (0 pages)  K (2 pages)  L (86 pages)  8 (43 pages)  9 (140 pages)
FL A .png  A (441 pages)  CS (3 pages) GC (2 pages) GI (3 pages) GM (4 pages) GS (28 pages) NF (12 pages) NI (27 pages) NM (4 pages) NN (1 pages) NP (21 pages) NS (2 pages)  GM (5 pages) GS (9 pages) NI (9 pages) NM (2 pages) NN (1 pages) NP (1 pages) NS (1 pages)  CS (1 pages) GM (2 pages) GS (19 pages) NF (6 pages) NI (24 pages) NM (1 pages) NN (4 pages) NP (14 pages) NS (1 pages)  CS (1 pages) GS (5 pages) NI (6 pages) NM (1 pages) NP (3 pages) NS (2 pages)  GS (7 pages) NI (3 pages) NP (1 pages) NS (1 pages)  GS (2 pages) NI (1 pages)  GS (1 pages) NS (1 pages)  GS (2 pages)  NM (1 pages)  GS (3 pages) NI (41 pages) NM (2 pages) NP (23 pages) NR (2 pages) NS (8 pages)  GS (4 pages) NI (8 pages) NP (3 pages) NS (11 pages)  GM (4 pages) GS (10 pages) NC (17 pages) NF (1 pages) NI (23 pages) NM (17 pages) NN (2 pages) NP (4 pages) NR (4 pages) NS (9 pages)
FL B .png  B (26 pages)  GS (3 pages) NC (12 pages) NI (2 pages) NS (1 pages)  NP (1 pages) NS (1 pages)  GM (1 pages) GS (2 pages) NP (1 pages)  GS (1 pages)  NP (1 pages)
FL C .png  C (29 pages)  GS (1 pages) NI (3 pages) NM (3 pages) NS (1 pages)  GM (1 pages) NI (1 pages) NS (1 pages)  GS (1 pages) NF (2 pages) NI (2 pages) NS (1 pages)  GS (2 pages) NI (2 pages) NS (1 pages)  GS (2 pages) NS (1 pages)  NM (1 pages) NS (1 pages)  NS (1 pages)  NS (1 pages)
FL D .png  D (6 pages)  GS (2 pages) NS (1 pages)  NS (1 pages)  NS (1 pages)  NM (1 pages)
FL E .png  E (42 pages)  GI (1 pages) GS (3 pages) NS (7 pages)  NF (1 pages) NS (8 pages)  GS (1 pages) NS (5 pages)  NS (1 pages)  NS (6 pages)  GS (3 pages) NF (1 pages) NI (1 pages) NS (4 pages)
FL F .png  F (35 pages)  GS (2 pages) NI (1 pages) NS (5 pages)  NS (4 pages)  GS (1 pages) NI (1 pages) NS (7 pages)  GS (4 pages) NC (1 pages) NI (2 pages) NS (7 pages)
FL G .png  G (13 pages)  NS (4 pages)  NS (2 pages)  NS (1 pages)  NS (6 pages)
FL 1 .png  1 (78 pages)  CS (1 pages) GS (12 pages) NF (1 pages) NI (13 pages) NM (1 pages) NN (2 pages) NP (11 pages) NS (3 pages)  CS (1 pages) GS (3 pages) NF (1 pages) NI (3 pages) NP (3 pages) NS (1 pages)  NF (1 pages) NI (4 pages) NS (1 pages)  NC (1 pages)  GM (1 pages) GS (1 pages) NC (3 pages) NI (5 pages) NP (3 pages) NS (2 pages)
FL 2 .png  2 (7 pages)  NI (1 pages) NP (2 pages) NS (2 pages)  NF (1 pages) NP (1 pages)
FL 3 .png  3 (10 pages)  NS (1 pages)  GS (3 pages) NS (3 pages)  GS (1 pages)  NS (2 pages)
FL 4 .png  4 (1 pages)  NS (1 pages)
FL 9 .png  9 (6 pages)  GI (1 pages) NI (1 pages) NS (2 pages)  NS (1 pages)  NI (1 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 (7 pages) alpha-Hydroxy  HX (0 pages) beta-Hydroxy  HY (4 pages) Peltogynoid  PT (0 pages)
Retrocalchone  RT (0 pages) Dehydro-backbone  WX (0 pages) Additional rings  RN (0 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 (534 pages) O-glycoside  G (164 pages) C-glycoside  C (7 pages) O- & C-glycoside  D (0 pages)
no modification  S (283 pages)  19 (2 pages) 1A (3 pages) 1C (1 pages) 1L (1 pages) 2C (2 pages) 39 (2 pages) 3A (1 pages) 3C (3 pages) 4A (1 pages) 9A (2 pages) 9C (1 pages) A8 (11 pages) A9 (9 pages) AA (2 pages) AB (1 pages) AC (1 pages) AD (2 pages) AE (1 pages) AG (1 pages) AL (8 pages) BA (1 pages) BB (1 pages) CA (1 pages) CB (1 pages) CC (1 pages) CD (1 pages) CE (1 pages) CF (1 pages) CH (1 pages) CK (1 pages) DA (1 pages) DB (1 pages) DC (1 pages) E8 (6 pages) E9 (4 pages) EA (7 pages) EC (8 pages) EG (5 pages) EL (1 pages) F8 (7 pages) F9 (7 pages) FA (5 pages) FC (4 pages) G8 (1 pages) G9 (6 pages) GA (4 pages) GG (2 pages) HY (1 pages) QU (1 pages)  19 (1 pages) 1A (12 pages) 1C (3 pages) 3C (3 pages) 3G (1 pages) A8 (4 pages) A9 (10 pages) AA (28 pages) AB (9 pages) AC (19 pages) AD (5 pages) AE (7 pages) AF (2 pages) AG (1 pages) AI (2 pages) AL (3 pages) BA (3 pages) BC (2 pages) BE (1 pages) CA (1 pages) CC (1 pages) CD (2 pages) CE (2 pages) DA (2 pages) E9 (3 pages) EA (3 pages) EG (1 pages) F8 (1 pages) F9 (4 pages) FA (2 pages) HY (1 pages)  1A (1 pages) 1C (1 pages) AA (3 pages) AC (1 pages) AD (1 pages)
alkylated  M (57 pages)  1A (1 pages) A9 (17 pages) AA (4 pages) AB (2 pages) AC (1 pages) AD (1 pages) AK (1 pages) AL (2 pages) CA (3 pages) CF (1 pages) DE (1 pages) HY (2 pages) QU (3 pages)  19 (1 pages) A9 (4 pages) AA (4 pages) AB (5 pages) AC (2 pages) BC (1 pages) CB (1 pages)
prenylated  I (0 pages)  19 (5 pages) 1A (13 pages) 1C (3 pages) 1L (4 pages) 2C (1 pages) 99 (1 pages) 9A (1 pages) A8 (8 pages) A9 (23 pages) AA (27 pages) AB (9 pages) AC (24 pages) AD (6 pages) AE (3 pages) AF (1 pages) AL (41 pages) BA (2 pages) CA (3 pages) CB (1 pages) CC (2 pages) CD (2 pages) E9 (1 pages) F8 (1 pages) F9 (2 pages) FA (1 pages)  9A (1 pages) AA (3 pages) EA (1 pages)
cyclic prenylated  R (0 pages)  A9 (4 pages) AL (2 pages) QU (2 pages)
furano FL  F (27 pages)  1A (1 pages) 1C (1 pages) 1L (1 pages) 29 (1 pages) A9 (1 pages) AA (12 pages) AC (6 pages) CC (2 pages) E9 (1 pages) EC (1 pages)
pyrano FL  P (93 pages)  19 (3 pages) 1A (11 pages) 1C (3 pages) 29 (1 pages) 2C (2 pages) A8 (3 pages) A9 (4 pages) AA (21 pages) AB (1 pages) AC (14 pages) AD (3 pages) AE (1 pages) AL (23 pages) BB (1 pages) BC (1 pages) BF (1 pages)
furano & pyrano FL  D (0 pages)
prenylpropanoid  N (11 pages)  1A (2 pages) A9 (2 pages) AA (1 pages) AB (1 pages) AC (4 pages) QU (1 pages)
others  C (36 pages)  18 (1 pages) 19 (3 pages) A9 (17 pages) BA (12 pages) F9 (1 pages)  AA (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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