Category:FL
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Flavonoid is a class of plant secondary metabolites that have two benzene rings (each called A-ring and B-ring) connected by a chain of three carbons (Figure 1). [[Image:FL.gif|thumb|150px|right|Figure 1: The Backbone of Flavonoid Structure]] | Flavonoid is a class of plant secondary metabolites that have two benzene rings (each called A-ring and B-ring) connected by a chain of three carbons (Figure 1). [[Image:FL.gif|thumb|150px|right|Figure 1: The Backbone of Flavonoid Structure]] | ||
The carbon chain, corresponding to the numbers 2,3,4 in Figure 1, is linked to a hydroxyl group in the A-ring to form the C-ring. The class of flavonoids are usually determined by the modification pattern of the C-ring (Table 1). | The carbon chain, corresponding to the numbers 2,3,4 in Figure 1, is linked to a hydroxyl group in the A-ring to form the C-ring. The class of flavonoids are usually determined by the modification pattern of the C-ring (Table 1). | ||
| + | |||
| + | {| class="wikitable" border="1" cellpadding="2" cellspacing="1" margin: 1em 1em 1em 1em" | ||
| + | |- | ||
| + | !colspan="3"|1st Class | ||
| + | |- valign="top" | ||
| + | |align="center"|FL1:[[:Category:FL1|Aurone and Chalcone]]<br>[[Image:Fl1.png|100px]] | ||
| + | |align="center"|FL2:[[:Category:FL2|Flavanone]]<br>[[Image:Fl2.png|100px]] | ||
| + | |align="center"|FL3:[[:Category:FL3|Flavone]]<br>[[Image:Fl3.png|100px]] | ||
| + | |- valign="top" | ||
| + | | | ||
| + | {| class="collapsible collapsed" border="1" cellspacing="0" width="150" | ||
| + | |- | ||
| + | ! colspan="2"|2nd Class | ||
| + | |- | ||
| + | |FL1A||[[:Category:FL1A|Aurone]]<br>[[Image:Fl1a.png|90px]] | ||
| + | |- | ||
| + | |FL1B||[[:Category:FL1B|Auronol]]<br>[[Image:Fl1b.png|90px]] | ||
| + | |- | ||
| + | |FL1C||[[:Category:FL1C|Chalcone]]<br>[[Image:Fl1.png|90px]] | ||
| + | |- | ||
| + | |FL1D||[[:Category:FL1D|Dihydrochalcone]]<br>[[Image:Fl1d.png|120px]] | ||
| + | |} | ||
| + | || | ||
| + | {| class="collapsible collapsed" border="1" cellspacing="0" width="150" | ||
| + | |- | ||
| + | ! colspan="2"|2nd Class | ||
| + | |- | ||
| + | ||FL2F||[[:Category:FL2F|Flavanone]] | ||
| + | |} | ||
| + | || | ||
| + | {| class="collapsible collapsed" border="1" cellspacing="0" width="150" | ||
| + | |- | ||
| + | ! colspan="2"|2nd Class | ||
| + | |- | ||
| + | ||FL3F||[[:Category:FL3F|Flavone]] | ||
| + | |} | ||
| + | |- valign="top" | ||
| + | |align="center"|FL4: [[:Category:FL4|Dihydroflavonol]]<br>[[Image:Fl4.png|100px]] | ||
| + | |align="center"|FL5: [[:Category:FL5|Flavonol]]<br>[[Image:Fl5.png|100px]] | ||
| + | |align="center"|FL6: [[:Category:FL6|Flavan]]<br>[[Image:Fl6.png|100px]] | ||
| + | |- valign="top" | ||
| + | | | ||
| + | {| class="collapsible collapsed" border="1" cellspacing="0" width="150" | ||
| + | |- | ||
| + | ! colspan="2"|2nd Class | ||
| + | |- | ||
| + | ||FL4D||[[:Category:FL4D|Dihydroflavonol]] | ||
| + | |} | ||
| + | || | ||
| + | {| class="collapsible collapsed" border="1" cellspacing="0" width="150" | ||
| + | |- | ||
| + | ! colspan="2"|2nd Class | ||
| + | |- | ||
| + | ||FL5F||[[:Category:FL5F|Flavonol]] | ||
| + | |} | ||
| + | || | ||
| + | {| class="collapsible collapsed" border="1" cellspacing="0" width="150" | ||
| + | |- | ||
| + | ! colspan="2"|2nd Class | ||
| + | |- | ||
| + | |FL6F||[[:Category:FL6F|Flavan]]<br>[[Image:Fl6.png|90px]] | ||
| + | |- | ||
| + | |FL63||[[:Category:FL63|Flavan 3-ol]]<br>[[Image:Fl63.png|90px]] | ||
| + | |- | ||
| + | |FL64||[[:Category:FL64|Flavan 4-ol]]<br>[[Image:Fl64.png|90px]] | ||
| + | |- | ||
| + | |FL6D||[[:Category:FL6D|Flavan 3,4-diol]]<br>[[Image:Fl6d.png|90px]] | ||
| + | |} | ||
| + | |- valign="top" | ||
| + | |align="center"|FL7: [[:Category:FL7|Anthocyanin]]<br>[[Image:Fl7.png|100px]] | ||
| + | |align="center"|FLI: [[:Category:FLI|Isoflavonoid]]<br>[[Image:Fli.png|100px]] | ||
| + | |align="center"|FLN: [[:Category:FLN|Neoflavonoid]]<br>[[Image:Fln.png|75px]] | ||
| + | |- valign="top" | ||
| + | | | ||
| + | {| class="collapsible collapsed" border="1" cellspacing="0" width="150" | ||
| + | |- | ||
| + | ! colspan="2"|2nd Class | ||
| + | |- | ||
| + | |FL7A||[[:Category:FL7A|Anthocyanin]]<br>[[Image:Fl7.png|90px]] | ||
| + | |- | ||
| + | |FL7D||[[:Category:FL7D|3-Desoxyanthocyanin]]<br>[[Image:Fl7d.png|90px]] | ||
| + | |} | ||
| + | || | ||
| + | {| class="collapsible collapsed" border="1" cellspacing="0" width="150" | ||
| + | |- | ||
| + | ! colspan="2"|2nd Class | ||
| + | |- | ||
| + | |FLIA||[[:Category:FLIA|Isoflavone]]<br>[[Image:Fli.png|90px]] | ||
| + | |- | ||
| + | |FLIB||[[:Category:FLIB|Isoflavanone]]<br>[[Image:Flib.png|90px]] | ||
| + | |- | ||
| + | |FLIC||[[:Category:FLIC|Isoflavan]]<br>[[Image:Flic.png|90px]] | ||
| + | |- | ||
| + | |FLID||[[:Category:FLID|Pterocarpane]]<br>[[Image:Flid.png|90px]] | ||
| + | |- | ||
| + | |FLIE||[[:Category:FLIE|Coumestan]]<br>[[Image:Flie.png|90px]] | ||
| + | |- | ||
| + | |FLIF||[[:Category:FLIF|Rotenoid]]<br>[[Image:Flif.png|90px]] | ||
| + | |- | ||
| + | |FLIG||[[:Category:FLIG|Coumaranochromone]]<br>[[Image:Flig.png|90px]] | ||
| + | |- | ||
| + | |FLIH||[[:Category:FLIH|3-Arylcoumarin]]<br>[[Image:Flih.png|90px]] | ||
| + | |- | ||
| + | |FLII||[[:Category:FLII|2-Arylbenzofuran]]<br>[[Image:Flii.png|90px]] | ||
| + | |- | ||
| + | |FLIJ||[[:Category:FLIJ|alpha-Methoxynbenzoin]]<br>[[Image:Flij.png|90px]] | ||
| + | |} | ||
| + | || | ||
| + | {| class="collapsible collapsed" border="1" cellspacing="0" width="150" | ||
| + | |- | ||
| + | ! colspan="2"|2nd Class | ||
| + | |- | ||
| + | |FLNA||[[:Category:FLNA|4-Arylcoumarin]]<br>[[Image:Fln.png|72px]] | ||
| + | |- | ||
| + | |FLNB||[[:Category:FLNB|4-Arylchroman]]<br>[[Image:Flnb.png|72px]] | ||
| + | |- | ||
| + | |FLNC||[[:Category:FLNC|Dalbergiquinol]]<br>[[Image:Flnc.png|72px]] | ||
| + | |- | ||
| + | |FLND||[[:Category:FLND|Dalbergione]]<br>[[Image:Flnd.png|65px]] | ||
| + | |- | ||
| + | |FLNE||[[:Category:FLNE|Neoflavene]]<br>[[Image:Flne.png|50px]] | ||
| + | |- | ||
| + | |FLNF||[[:Category:FLNF|Coumarinic acid]]<br>[[Image:Flnf.png|72px]] | ||
| + | |} | ||
| + | |} | ||
| + | |||
{| class="wikitable" border="1" cellpadding="2" cellspacing="1" margin: 1em 1em 1em 1em" | {| class="wikitable" border="1" cellpadding="2" cellspacing="1" margin: 1em 1em 1em 1em" | ||
Revision as of 07:09, 8 March 2008
FL: Flavonoid
Structural Characteristics
Flavonoid is a class of plant secondary metabolites that have two benzene rings (each called A-ring and B-ring) connected by a chain of three carbons (Figure 1).The carbon chain, corresponding to the numbers 2,3,4 in Figure 1, is linked to a hydroxyl group in the A-ring to form the C-ring. The class of flavonoids are usually determined by the modification pattern of the C-ring (Table 1).
| 1st Class | ||||||||||||||||||||||||||||||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| FL1:Aurone and Chalcone |
FL2:Flavanone |
FL3:Flavone | ||||||||||||||||||||||||||||||||||||||||||
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| FL4: Dihydroflavonol |
FL5: Flavonol |
FL6: Flavan | ||||||||||||||||||||||||||||||||||||||||||
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| FL7: Anthocyanin |
FLI: Isoflavonoid |
FLN: Neoflavonoid | ||||||||||||||||||||||||||||||||||||||||||
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| 1st Class | 2nd Class | ||
|---|---|---|---|
| FL1 | Aurone and Chalcone |
FL1A | Aurone |
| FL1B | Auronol | ||
| FL1C | Chalcone | ||
| FL1D | Dihydrochalcone | ||
| FL2 | Flavanone |
FL2F | Flavanone |
| FL3 | Flavone |
FL3F | Flavone |
| FL4 | Dihydroflavonol |
FL4D | Dihydroflavonol |
| FL5 | Flavonol |
FL5F | Flavonol |
| FL6 | Flavan |
FL6F | Flavan |
| FL63 | Flavan 3-ol | ||
| FL64 | Flavan 4-ol | ||
| FL6D | Flavan 3,4-diol | ||
| FL7 | Anthocyanin |
FL7A | Anthocyanin |
| FL7D | 3-Desoxyanthocyanin | ||
| FLI | Isoflavonoid |
FLIA | Isoflavone |
| FLIB | Isoflavanone | ||
| FLIC | Isoflavan | ||
| FLID | Pterocarpane | ||
| FLIE | Coumestan | ||
| FLIF | Rotenoid | ||
| FLIG | Coumaranochromone | ||
| FLIH | 3-Arylcoumarin | ||
| FLII | 2-Arylbenzofuran | ||
| FLIJ | alpha-Methoxynbenzoin | ||
| FLN | Neoflavonoid |
FLNA | 4-Arylcoumarin |
| FLNB | 4-Arylchroman | ||
| FLNC | Dalbergiquinol | ||
| FLND | Dalbergione | ||
| FLNE | Neoflavene | ||
| FLNF | Coumarinic acid | ||
Biosynthesis
Flavonoid is synthesized through the phenylpropanoid-acetate pathway in all higher plants. It is responsible for many biological activities including pigments, anti-oxidative or anti-allergic agents, and signaling elements in nodule formation. Some of them are quite familiar in our daily life.
Familiar examples.
anthocyanin (blueberry), isoflavone (soybean), rutin (soba noodle), catechin (tea), flavan-diol (tea), naringeninchalcone (tomato), polyphenol (wine, cacao)
Subcategories
This category has the following 10 subcategories, out of 10 total.