Category:FL1C

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(Replacing page with '{{Hierarchy|{{PAGENAME}}}} ===FL1C: Chalcone=== {{FL_digit56|FL1C}}')
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{{Hierarchy|{{PAGENAME}}}}
 
{{Hierarchy|{{PAGENAME}}}}
 
===FL1C: Chalcone===
 
===FL1C: Chalcone===
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{{FL_digit56}}
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{{FL_digit56|FL1C}}
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<!---
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{{ClassifiedTable|
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FL1C&&Chalcone&&
+
−
&&FL1C18&&2,(3),(5),(6),2',4'-Hydroxychalcone and O-methyl derivatives&&
+
−
&&FL1C18NP&&Pyranoflavonoid&&
+
−
&&FL1C19&&(3),(5),2',4'-Hydroxychalcone and O-methyl derivatives&&
+
−
&&FL1C19NF&&Furanoflavonoid&&
+
−
&&FL1C19NI&&Non-cyclic prenyl substituted&&
+
−
&&FL1C19NP&&Pyranoflavonoid&&
+
−
&&FL1C19NS&&Simple substitution&&
+
−
&&FL1C1A&&Isoliquiritigenin and O-methyl derivatives&&
+
−
&&FL1C1ACS&&C-Glycoside&&
+
−
&&FL1C1AGS&&O-Glycoside&&
+
−
&&FL1C1AND&&Furano and pyrano substituted&&
+
−
&&FL1C1ANF&&Furanoflavonoid&&
+
−
&&FL1C1ANI&&Non-cyclic prenyl substituted&&
+
−
&&FL1C1ANM&&C-Methyl or C2/C3 substituted&&
+
−
&&FL1C1ANN&&Flavonophenylpropanoid&&
+
−
&&FL1C1ANP&&Pyranoflavonoid&&
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−
&&FL1C1ANS&&Simple substitution&&
+
−
&&FL1C1C&&Butein and O-methyl derivatives&&
+
−
&&FL1C1CGS&&O-Glycoside&&
+
−
&&FL1C1CNF&&Furanoflavonoid&&
+
−
&&FL1C1CNI&&Non-cyclic prenyl substituted&&
+
−
&&FL1C1CNP&&Pyranoflavonoid&&
+
−
&&FL1C1CNS&&Simple substitution&&
+
−
&&FL1C1G&&Robtein and O-methyl derivatives&&
+
−
&&FL1C1GNS&&Simple substitution&&
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−
&&FL1C1L&&2,(3),4,(5),(6),2',4'-Hydroxychalcone and O-methyl derivatives&&
+
−
&&FL1C1LNI&&Non-cyclic prenyl substituted&&
+
−
&&FL1C1LNP&&Pyranoflavonoid&&
+
−
&&FL1C1LNS&&Simple substitution&&
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−
&&FL1C28&&2,(3),(5),(6),2',4',5'-Hydroxychalcone and O-methyl derivatives&&
+
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&&FL1C28NI&&Non-cyclic prenyl substituted&&
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−
&&FL1C28NP&&Pyranoflavonoid&&
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−
&&FL1C29&&(3),(5),2',4',5'-Hydroxychalcone and O-methyl derivatives&&
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&&FL1C29NP&&Pyranoflavonoid&&
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−
&&FL1C29NS&&Simple substitution&&
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&&FL1C2A&&4,2',4',5'-Tetrahydroxychalcone and O-methyl derivatives&&
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&&FL1C2ANP&&Pyranoflavonoid&&
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−
&&FL1C2C&&Neoplathymenin and O-methyl derivatives&&
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−
&&FL1C2CGS&&O-Glycoside&&
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−
&&FL1C2CNF&&Furanoflavonoid&&
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−
&&FL1C2CNP&&Pyranoflavonoid&&
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−
&&FL1C2CNS&&Simple substitution&&
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−
&&FL1C39&&(3),(5),2',3',4'-Hydroxychalcone and O-methyl derivatives&&
+
−
&&FL1C39NS&&Simple substitution&&
+
−
&&FL1C3A&&4,2',3',4'-Tetrahydroxychalcone and O-Methyl derivatives&&
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−
&&FL1C3AGS&&O-Glycoside&&
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−
&&FL1C3ANS&&Simple substitution&&
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−
&&FL1C3C&&Okanin and O-methyl derivatives&&
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−
&&FL1C3CGS&&O-Glycoside&&
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−
&&FL1C3CNS&&Simple substitution&&
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&&FL1C98&&2,(3),(5),(6),(2'),(3'),(5'),(6')-Hydroxychalcone and O-methyl derivatives&&
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&&FL1C98NI&&Non-cyclic prenyl substituted&&
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&&FL1C98NS&&Simple substitution&&
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&&FL1C99&&4'-Desoxychalcone (2,4-Desoxy) and O-methyl derivatives&&
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&&FL1C99GS&&O-Glycoside&&
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−
&&FL1C99NS&&Simple substitution&&
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&&FL1C9A&&4,(2'),(3'),(5'),(6')-Hydroxychalcone and O-methyl derivatives&&
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&&FL1C9AGS&&O-Glycoside&&
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−
&&FL1C9ANP&&Pyranoflavonoid&&
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−
&&FL1C9ANS&&Simple substitution&&
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&&FL1C9C&&3,4,(2'),(3'),(5'),(6')-Hydroxychalcone and O-methyl derivatives&&
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&&FL1C9CGS&&O-Glycoside&&
+
−
&&FL1C9CNS&&Simple substitution&&
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−
&&FL1C9G&&3,4,5,(2'),(3'),(5'),(6')-Hydroxychalcone and O-methyl derivatives&&
+
−
&&FL1C9GNS&&Simple substitution&&
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−
&&FL1CA8&&2,(3),(5),(6),2',4',6'-Hydroxychalcone&&
+
−
&&FL1CA8GS&&O-Glycoside&&
+
−
&&FL1CA8NI&&Non-cyclic prenyl substituted&&
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&&FL1CA8NP&&Pyranoflavonoid&&
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−
&&FL1CA8NS&&Simple substitution&&
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&&FL1CA9&&(3),(5),2',4',6'-Hydroxychalcone&&
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&&FL1CA9NC&&Flavonoid substituted by complex substituent&&
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&&FL1CA9NF&&Furanoflavonoid&&
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&&FL1CA9NI&&Non-cyclic prenyl substituted&&
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&&FL1CA9NM&&C-Methyl or C2/C3 substituted&&
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&&FL1CA9NN&&Flavonophenylpropanoid&&
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&&FL1CA9NP&&Pyranoflavonoid&&
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&&FL1CA9NR&&Ring containing prenyl substituted&&
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&&FL1CA9NS&&Simple substitution&&
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&&FL1CAA&&Naringenin chalcone&&
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&&FL1CAAGS&&O-Glycoside&&
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&&FL1CAANI&&Non-cyclic prenyl substituted&&
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−
&&FL1CAANN&&Flavonophenylpropanoid&&
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&&FL1CAANP&&Pyranoflavonoid&&
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−
&&FL1CAANS&&Simple substitution&&
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−
&&FL1CAB&&2',4',6'-Trihydroxy-4-methoxychalcone&&
+
−
&&FL1CABNS&&Simple substitution&&
+
−
&&FL1CAC&&3,4,2',4',6'-Pentahydroxychalcone&&
+
−
&&FL1CACGS&&O-Glycoside&&
+
−
&&FL1CACNN&&Flavonophenylpropanoid&&
+
−
&&FL1CACNP&&Pyranoflavonoid&&
+
−
&&FL1CACNR&&Ring containing prenyl substituted&&
+
−
&&FL1CACNS&&Simple substitution&&
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−
&&FL1CAD&&4,2',4',6'-Tetrahydroxy-3-methoxychalcone&&
+
−
&&FL1CADGS&&O-Glycoside&&
+
−
&&FL1CADNI&&Non-cyclic prenyl substituted&&
+
−
&&FL1CADNS&&Simple substitution&&
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−
&&FL1CAE&&3,2',4',6'-Tetrahydroxy-4-methoxychalcone&&
+
−
&&FL1CAENI&&Non-cyclic prenyl substituted&&
+
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&&FL1CAENR&&Ring containing prenyl substituted&&
+
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&&FL1CAF&&2',4',6'-Trihydroxy-3,4-dimethoxychalcone&&
+
−
&&FL1CAFNR&&Ring containing prenyl substituted&&
+
−
&&FL1CAG&&3,4,5,2',4',6'-Hexahydroxychalcone&&
+
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&&FL1CAGGS&&O-Glycoside&&
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−
&&FL1CAL&&2,4,2',4',6'-Hydroxychalcone and O-methyl derivatives&&
+
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&&FL1CALGS&&O-Glycoside&&
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−
&&FL1CALNI&&Non-cyclic prenyl substituted&&
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−
&&FL1CALNS&&Simple substitution&&
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&&FL1CBA&&Helichrysetin&&
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−
&&FL1CBAGS&&O-Glycoside&&
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−
&&FL1CBANC&&Flavonoid substituted by complex substituent&&
+
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&&FL1CBANI&&Non-cyclic prenyl substituted&&
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−
&&FL1CBANP&&Pyranoflavonoid&&
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−
&&FL1CBANS&&Simple substitution&&
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&&FL1CBB&&4',6'-Dihydroxy-4,2'-methoxychalcone&&
+
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&&FL1CBBNP&&Pyranoflavonoid&&
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&&FL1CBC&&3,4,4',6'-Tetrahydroxy-2'-methoxychalcone&&
+
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&&FL1CBCNP&&Pyranoflavonoid&&
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&&FL1CBE&&3,4',6'-Trihydroxy-4,2'-dimethoxychalcone&&
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&&FL1CBEGS&&O-Glycoside&&
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−
&&FL1CBF&&4',6'-Dihydroxy-3,4,2'-trimethoxychalcone&&
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&&FL1CBFNP&&Pyranoflavonoid&&
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&&FL1CCA&&Neosakuranetin&&
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−
&&FL1CCAGS&&O-Glycoside&&
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−
&&FL1CCANI&&Non-cyclic prenyl substituted&&
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−
&&FL1CCANP&&Pyranoflavonoid&&
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−
&&FL1CCANS&&Simple substitution&&
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−
&&FL1CCB&&Gymnogrammene&&
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&&FL1CCBNP&&Pyranoflavonoid&&
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−
&&FL1CCBNS&&Simple substitution&&
+
−
&&FL1CCBNS0&&Normal&&
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−
&&FL1CCBNSH&&Halogen incluted&&
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&&FL1CCD&&4,2',6'-Trihydroxy-3,4'-dimethoxychalcone&&
+
−
&&FL1CCDNS&&Simple substitution&&
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−
&&FL1CCF&&2',6'-Dihydroxy-3,4,4'-trimethoxychalcone&&
+
−
&&FL1CCFNP&&Pyranoflavonoid&&
+
−
&&FL1CDA&&Naringenin chalcone O-methyl derivatives (4-Hydroxy, without FL1CBA, FL1CCA)&&
+
−
&&FL1CDAGS&&O-Glycoside&&
+
−
&&FL1CDANI&&Non-cyclic prenyl substituted&&
+
−
&&FL1CDANS&&Simple substitution&&
+
−
&&FL1CDB&&Naringenin chalcone O-methyl derivatives (4-Methoxy, without FL1CAB, FL1CBB, FL1CCB)&&
+
−
&&FL1CDBNS&&Simple substitution&&
+
−
&&FL1CDC&&3,4,2',4',6'-Pentahydroxychalcone O-methyl derivatives (3,4-Hydroxy, without FL1CBC)&&
+
−
&&FL1CDCNI&&Non-cyclic prenyl substituted&&
+
−
&&FL1CDCNS&&Simple substitution&&
+
−
&&FL1CDD&&3,4,2',4',6'-Pentahydroxychalcone O-methyl derivatives (4-Hydroxy-3-methoxy, without FL1CAD, FL1CCD)&&
+
−
&&FL1CDDGS&&O-Glycoside&&
+
−
&&FL1CDE&&3,4,2',4',6'-Pentahydroxychalcone O-methyl derivatives (3-Hydroxy-4-methoxy, without FL1CAE)&&
+
−
&&FL1CDENS&&Simple substitution&&
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−
&&FL1CDF&&3,4,2',4',6'-Pentahydroxychalcone O-methyl derivatives (3,4-Methoxy, without FL1CAF)&&
+
−
&&FL1CDFNS&&Simple substitution&&
+
−
&&FL1CDK&&3,4,5,2',4',6'-Hexahydroxychalcone O-methylderivatives (Without FL1CAH-FL1CAK, FL1CBG-FL1CBK, FL1CCG-FL1CCK, FL1CDG-FL1CDL)&&
+
−
&&FL1CDKNS&&Simple substitution&&
+
−
&&FL1CE8&&2,(3),(5),(6),2',3',4',6'-Hydroxychalcone and O-methyl derivatives&&
+
−
&&FL1CE8NS&&Simple substitution&&
+
−
&&FL1CE9&&(3),(5),2',3',4',6'-Hydroxychalcone and O-methyl derivatives&&
+
−
&&FL1CE9NC&&Flavonoid substituted by complex substituent&&
+
−
&&FL1CE9NI&&Non-cyclic prenyl substituted&&
+
−
&&FL1CE9NP&&Pyranoflavonoid&&
+
−
&&FL1CE9NS&&Simple substitution&&
+
−
&&FL1CEA&&4,2',3',4',6'-Pentahydroxychalcone and O-methyl derivatives&&
+
−
&&FL1CEANS&&Simple substitution&&
+
−
&&FL1CEC&&3,4,2',3',4',6'-Hexahydroxychalcone and O-methyl derivatives&&
+
−
&&FL1CECNS&&Simple substitution&&
+
−
&&FL1CEL&&2,(3),4,(5),(6),2',3',4',6'-Hydroxychalcone and O-methyl derivatives&&
+
−
&&FL1CELNS&&Simple substitution&&
+
−
&&FL1CG9&&(3),(5),2',3',4',5',6'-Hydroxychalcone and O-methyl derivatives&&
+
−
&&FL1CG9NI&&Non-cyclic prenyl substituted&&
+
−
&&FL1CG9NS&&Simple substitution&&
+
−
&&FL1CGA&&4,2',3',4',5',6'-Hexahydroxychalcone and O-methyl derivatives&&
+
−
&&FL1CGANS&&Simple substitution&&
+
−
&&FL1CHX&&alpha-Hydroxychalcone&&
+
−
&&FL1CHXGS&&O-Glycoside&&
+
−
&&FL1CHXNS&&Simple substitution&&
+
−
&&FL1CHY&&beta-Hydroxychalcone&&
+
−
&&FL1CHYGS&&O-Glycoside&&
+
−
&&FL1CHYNF&&Furanoflavonoid&&
+
−
&&FL1CHYNI&&Non-cyclic prenyl substituted&&
+
−
&&FL1CHYNM&&C-Methyl or C2/C3 substituted&&
+
−
&&FL1CHYNP&&Pyranoflavonoid&&
+
−
&&FL1CHYNS&&Simple substitution&&
+
−
&&FL1CPT&&Peltogynoid chalcone&&
+
−
&&FL1CPTNS&&Simple substitution&&
+
−
&&FL1CQU&&Quinochalcone&&
+
−
&&FL1CQUCC&&Flavonoid C-glycoside substituted by complex substituent&&
+
−
&&FL1CQUCCN&&Nitrogen incluted&&
+
−
&&FL1CQUCN&&Flavonophenylpropanoid C-glycoside&&
+
−
&&FL1CQUCS&&C-Glycoside&&
+
−
&&FL1CQUGS&&O-Glycoside&&
+
−
&&FL1CQUNC&&Flavonoid substituted by complex substituent&&
+
−
&&FL1CQUNI&&Non-cyclic prenyl substituted&&
+
−
&&FL1CQUNM&&C-Methyl or C2/C3 substituted&&
+
−
&&FL1CQUNS&&Simple substitution&&
+
−
&&FL1CRT&&Retrochalcone&&
+
−
&&FL1CRTNF&&Furanoflavonoid&&
+
−
&&FL1CRTNI&&Non-cyclic prenyl substituted&&
+
−
&&FL1CRTNM&&C-Methyl or C2/C3 substituted&&
+
−
&&FL1CRTNP&&Pyranoflavonoid&&
+
−
&&FL1CRTNS&&Simple substitution&&
+
−
&&FL1CUN&&Unusual core chalcone&&
+
−
&&FL1CUNNS&&Simple substitution&&
+
−
}}
+
−
--->
+

Revision as of 17:36, 20 March 2008


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

Upper classes : FL Flavonoid : FL1 Aurone and Chalcone

Contents

FL1C: Chalcone

Fl1c.png


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。

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 (148 pages)  B (7 pages)  C (68 pages)  D (5 pages)  E (5 pages)  F (4 pages)  G (3 pages)  H (0 pages)  I (0 pages)  J (0 pages)  K (1 pages)  L (23 pages)  8 (17 pages)  9 (84 pages)
FL A .png  A (89 pages)  GS (9 pages) NI (2 pages) NN (1 pages) NP (5 pages) NS (1 pages)  NS (1 pages)  GS (2 pages) NN (1 pages) NP (1 pages) NR (1 pages) NS (1 pages)  GS (1 pages) NI (1 pages) NS (1 pages)  NI (2 pages) NR (1 pages)  NR (1 pages)  GS (1 pages)  GS (1 pages) NI (3 pages) NS (4 pages)  GS (1 pages) NI (1 pages) NP (3 pages) NS (3 pages)  NC (1 pages) NF (5 pages) NI (8 pages) NM (6 pages) NN (1 pages) NP (12 pages) NR (3 pages) NS (4 pages)
FL B .png  B (18 pages)  GS (4 pages) NC (2 pages) NI (3 pages) NP (3 pages) NS (2 pages)  NP (1 pages)  NP (1 pages)  GS (1 pages)  NP (1 pages)
FL C .png  C (9 pages)  GS (1 pages) NI (1 pages) NP (1 pages) NS (1 pages)  NP (1 pages) NS (2 pages)  NS (1 pages)  NP (1 pages)
FL D .png  D (15 pages)  GS (3 pages) NI (1 pages) NS (2 pages)  NS (2 pages)  NI (1 pages) NS (2 pages)  GS (1 pages)  NS (1 pages)  NS (1 pages)  NS (1 pages)
FL E .png  E (26 pages)  NS (4 pages)  NS (4 pages)  NS (5 pages)  NS (1 pages)  NC (1 pages) NI (3 pages) NP (1 pages) NS (7 pages)
FL F .png  F (0 pages)
FL G .png  G (10 pages)  NS (2 pages)  NI (3 pages) NS (5 pages)
FL 1 .png  1 (128 pages)  CS (1 pages) GS (11 pages) ND (2 pages) NF (5 pages) NI (34 pages) NM (2 pages) NN (2 pages) NP (20 pages) NS (5 pages)  GS (4 pages) NF (1 pages) NI (2 pages) NP (3 pages) NS (7 pages)  NS (1 pages)  NI (7 pages) NP (2 pages) NS (1 pages)  NP (1 pages)  NF (5 pages) NI (4 pages) NP (5 pages) NS (3 pages)
FL 2 .png  2 (16 pages)  NP (3 pages)  GS (1 pages) NF (1 pages) NP (1 pages) NS (2 pages)  NI (2 pages) NP (3 pages)  NP (2 pages) NS (1 pages)
FL 3 .png  3 (40 pages)  GS (5 pages) NS (4 pages)  GS (26 pages) NS (4 pages)  NS (1 pages)
FL 4 .png  4 (0 pages)
FL 9 .png  9 (14 pages)  GS (2 pages) NP (1 pages) NS (3 pages)  GS (1 pages) NS (1 pages)  NS (1 pages)  NI (1 pages) NS (1 pages)  GS (1 pages) NS (2 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;

Other Unusual Patterns

These types are not classified in the above chart.

Quinone  QU (15 pages) alpha-Hydroxy  HX (2 pages) beta-Hydroxy  HY (37 pages) Peltogynoid  PT (2 pages)
Retrocalchone  RT (15 pages) Dehydro-backbone  WX (0 pages) Additional rings  RN (0 pages) Others  UN (4 pages)
Pyranoanthocyanin (FL7 only)  RX (0 pages)

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 (355 pages) O-glycoside  G (81 pages) C-glycoside  C (4 pages) O- & C-glycoside  D (0 pages)
no modification  S (204 pages)  19 (3 pages) 1A (5 pages) 1C (7 pages) 1G (1 pages) 1L (1 pages) 29 (1 pages) 2C (2 pages) 39 (1 pages) 3A (4 pages) 3C (4 pages) 98 (1 pages) 99 (2 pages) 9A (3 pages) 9C (1 pages) 9G (1 pages) A8 (3 pages) A9 (4 pages) AA (1 pages) AB (1 pages) AC (1 pages) AD (1 pages) AL (4 pages) BA (2 pages) CA (1 pages) CB (2 pages) CD (1 pages) DA (2 pages) DB (2 pages) DC (2 pages) DE (1 pages) DF (1 pages) DK (1 pages) E8 (1 pages) E9 (7 pages) EA (4 pages) EC (4 pages) EL (5 pages) G9 (5 pages) GA (2 pages) HX (1 pages) HY (10 pages) PT (2 pages) QU (3 pages) RT (6 pages) UN (4 pages)  1A (11 pages) 1C (4 pages) 2C (1 pages) 3A (5 pages) 3C (26 pages) 99 (1 pages) 9A (2 pages) 9C (1 pages) A8 (1 pages) AA (9 pages) AC (2 pages) AD (1 pages) AG (1 pages) AL (1 pages) BA (4 pages) BE (1 pages) CA (1 pages) DA (3 pages) DD (1 pages) HX (1 pages) HY (3 pages) QU (1 pages)  1A (1 pages) QU (1 pages)
alkylated  M (17 pages)  1A (2 pages) A9 (6 pages) HY (3 pages) QU (5 pages) RT (1 pages)
prenylated  I (0 pages)  19 (4 pages) 1A (34 pages) 1C (2 pages) 1L (7 pages) 28 (2 pages) 98 (1 pages) A8 (1 pages) A9 (8 pages) AA (2 pages) AD (1 pages) AE (2 pages) AL (3 pages) BA (3 pages) CA (1 pages) DA (1 pages) DC (1 pages) E9 (3 pages) G9 (3 pages) HY (7 pages) QU (2 pages) RT (4 pages)
cyclic prenylated  R (0 pages)  A9 (3 pages) AC (1 pages) AE (1 pages) AF (1 pages)
furano FL  F (22 pages)  19 (5 pages) 1A (5 pages) 1C (1 pages) 2C (1 pages) A9 (5 pages) HY (4 pages) RT (1 pages)
pyrano FL  P (85 pages)  18 (1 pages) 19 (5 pages) 1A (20 pages) 1C (3 pages) 1L (2 pages) 28 (3 pages) 29 (2 pages) 2A (3 pages) 2C (1 pages) 9A (1 pages) A8 (3 pages) A9 (12 pages) AA (5 pages) AC (1 pages) BA (3 pages) BB (1 pages) BC (1 pages) BF (1 pages) CA (1 pages) CB (1 pages) CF (1 pages) E9 (1 pages) HY (10 pages) RT (3 pages)
furano & pyrano FL  D (2 pages)  1A (2 pages)
prenylpropanoid  N (6 pages)  1A (2 pages) A9 (1 pages) AA (1 pages) AC (1 pages)  QU (1 pages)
others  C (6 pages)  A9 (1 pages) BA (2 pages) E9 (1 pages) QU (1 pages)  QU (1 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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