Category:FL
Line 20: | Line 20: | ||
|FL1D||[[:Category:FL1D|Dihydrochalcone]] | |FL1D||[[:Category:FL1D|Dihydrochalcone]] | ||
|- | |- | ||
− | |FL2||[[:Category:FL2|Flavanone]]<br>[[Image: | + | |FL2||[[:Category:FL2|Flavanone]]<br>[[Image:Fl2.png|100px]]||FL2F||[[:Category:FL2F|Flavanone]] |
|- | |- | ||
− | |FL3||[[:Category:FL3|Flavone]]<br>[[Image:Fl3. | + | |FL3||[[:Category:FL3|Flavone]]<br>[[Image:Fl3.png|100px]]||FL3F||[[:Category:FL3F|Flavone]] |
|- | |- | ||
− | |FL4||[[:Category:FL4|Dihydroflavonol]]<br>[[Image:Fl4. | + | |FL4||[[:Category:FL4|Dihydroflavonol]]<br>[[Image:Fl4.png|100px]]||FL4D||[[:Category:FL4D|Dihydroflavonol]] |
|- | |- | ||
− | |FL5||[[:Category:FL5|Flavonol]]<br>[[Image:Fl5. | + | |FL5||[[:Category:FL5|Flavonol]]<br>[[Image:Fl5.png|100px]]||FL5F||[[:Category:FL5F|Flavonol]] |
|- | |- | ||
|rowspan="4"|FL6 | |rowspan="4"|FL6 | ||
− | |rowspan="4"|[[:Category:FL6|Flavan]]<br>[[Image:Fl6. | + | |rowspan="4"|[[:Category:FL6|Flavan]]<br>[[Image:Fl6.png|100px]] |
|FL6F||[[:Category:FL6F|Flavan]] | |FL6F||[[:Category:FL6F|Flavan]] | ||
|- | |- | ||
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|- | |- | ||
|rowspan="2"|FL7 | |rowspan="2"|FL7 | ||
− | |rowspan="2"|[[:Category:FL7|Anthocyanin]]<br>[[Image:Fl7. | + | |rowspan="2"|[[:Category:FL7|Anthocyanin]]<br>[[Image:Fl7.png|100px]] |
|FL7A||[[:Category:FL7A|Anthocyanin]] | |FL7A||[[:Category:FL7A|Anthocyanin]] | ||
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|- | |- | ||
|rowspan="10"|FLI | |rowspan="10"|FLI | ||
− | |rowspan="10"|[[:Category:FLI|Isoflavonoid]]<br>[[Image:Fli. | + | |rowspan="10"|[[:Category:FLI|Isoflavonoid]]<br>[[Image:Fli.png|100px]] |
|FLIA||[[:Category:FLIA|Isoflavone]] | |FLIA||[[:Category:FLIA|Isoflavone]] | ||
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|- | |- | ||
|rowspan="6"|FLN | |rowspan="6"|FLN | ||
− | |rowspan="6"|[[:Category:FLN|Neoflavonoid]]<br>[[Image:Fln. | + | |rowspan="6"|[[:Category:FLN|Neoflavonoid]]<br>[[Image:Fln.png|70px]] |
|FLNA||[[:Category:FLNA|4-Arylcoumarin]] | |FLNA||[[:Category:FLNA|4-Arylcoumarin]] | ||
|- | |- |
Revision as of 11:09, 3 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).
FLx | FLxy | ||
---|---|---|---|
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.