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Aureusidin
Aureusidin is an aurone, a type of flavonoid. Metabolism Aureusidin synthase is an enzyme found in ''Antirrhinum majus ''Antirrhinum majus'', the common snapdragon (often - especially in horticulture - simply "snapdragon"), is a species of flowering plant belonging to the genus ''Antirrhinum''. The plant was placed in the family Plantaginaceae following a revis ...'' (Garden snapdragon). References Aurones Catechols Resorcinols {{Aromatic-stub ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Aureusidin Synthase
Aureusidin synthase (, ''AmAS1'') is an enzyme with systematic name ''2',4,4',6'-tetrahydroxychalcone 4'-O-beta-D-glucoside:oxygen oxidoreductase''. Aureusidin synthase has two main enzymatic tasks: hydroxylation at the 3-position on the B-ring of chalcones, and the oxidative cyclization of chalcones to form aurones. The chalcones modified are typically glucosylated 2',4,4',6'-tetrahydroxychalcone (THC) and 2',3,4,4',6'-pentahydroxychalcone (PHC). These aurones, particularly auresidin, form pigments for coloration in flowers. These pigments may have been developed to attract and guide bees for pollination, but they also provide protection from viruses, pests and fungus. Enzyme structure Aureusidin synthase is a 39 kDa monomeric glycoprotein containing binuclear copper. The addition of phenylthiourea, which competitively binds to binuclear copper, inhibits the enzyme's productivity overall. Because of this, it is likely that the active site contains the binuclear copper. ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Aurones
An aurone is a heterocyclic chemical compound which is a type of flavonoid. There are two isomers of the molecule, with (''E'')- and (''Z'')-configurations. The molecule contains a benzofuran element associated with a benzylidene linked in position 2. In aurone, a chalcone-like group is closed into a 5-membered ring instead of the 6-membered ring more typical of flavonoids. Aurone derivatives Aurone forms the core for a family of derivatives which are known collectively as aurones. Aurones are plant flavonoids that provide yellow color to the flowers of some popular ornamental plants, such as snapdragon and cosmos. Aurones including 4'-chloro-2-hydroxyaurone (C15H11O3Cl) and 4'-chloroaurone (C15H9O2Cl) can also be found in the brown alga ''Spatoglossum variabile''. Most aurones are in a (''Z'')-configuration, which is the more stable configuration according to Austin Model 1 computation, but there are also some in the (''E'')-configurations such as (E)-3'-O-β-d-glucop ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Aurones
An aurone is a heterocyclic chemical compound which is a type of flavonoid. There are two isomers of the molecule, with (''E'')- and (''Z'')-configurations. The molecule contains a benzofuran element associated with a benzylidene linked in position 2. In aurone, a chalcone-like group is closed into a 5-membered ring instead of the 6-membered ring more typical of flavonoids. Aurone derivatives Aurone forms the core for a family of derivatives which are known collectively as aurones. Aurones are plant flavonoids that provide yellow color to the flowers of some popular ornamental plants, such as snapdragon and cosmos. Aurones including 4'-chloro-2-hydroxyaurone (C15H11O3Cl) and 4'-chloroaurone (C15H9O2Cl) can also be found in the brown alga ''Spatoglossum variabile''. Most aurones are in a (''Z'')-configuration, which is the more stable configuration according to Austin Model 1 computation, but there are also some in the (''E'')-configurations such as (E)-3'-O-β-d-glucop ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Flavonoid
Flavonoids (or bioflavonoids; from the Latin word ''flavus'', meaning yellow, their color in nature) are a class of polyphenolic secondary metabolites found in plants, and thus commonly consumed in the diets of humans. Chemically, flavonoids have the general structure of a 15-carbon skeleton, which consists of two phenyl rings (A and B) and a heterocyclic ring (C, the ring containing the embedded oxygen). This carbon structure can be abbreviated C6-C3-C6. According to the IUPAC nomenclature, they can be classified into: *flavonoids or bioflavonoids *isoflavonoids, derived from 3-phenyl chromen-4-one (3-phenyl-1,4-benzopyrone) structure *neoflavonoids, derived from 4-phenylcoumarine (4-phenyl-1,2-benzopyrone) structure The three flavonoid classes above are all ketone-containing compounds and as such, anthoxanthins ( flavones and flavonols). This class was the first to be termed bioflavonoids. The terms flavonoid and bioflavonoid have also been more loosely used to describe non ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Antirrhinum Majus
''Antirrhinum majus'', the common snapdragon (often - especially in horticulture - simply "snapdragon"), is a species of flowering plant belonging to the genus ''Antirrhinum''. The plant was placed in the family Plantaginaceae following a revision of its prior classical family, Scrophulariaceae. The common name "snapdragon", originates from the flowers' reaction to having their throats squeezed, which causes the "mouth" of the flower to snap open like a dragon's mouth. It is widely used as an ornamental plant in borders and as a cut flower. It is perennial but usually cultivated as an annual plant. The species has been in culture since the 15th century. Taxonomy There are five subspecies: *''Antirrhinum majus'' subsp. ''majus''. Southern France, northeast Spain. *''Antirrhinum majus'' subsp. ''cirrhigerum'' (Ficalho) Franco. Southern Portugal, southwest Spain. *''Antirrhinum majus'' subsp. ''linkianum'' (Boiss. & Reut.) Rothm. Western Portugal (endemic). *''Antirrhinum maju ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Catechols
Catechol ( or ), also known as pyrocatechol or 1,2-dihydroxybenzene, is a toxic organic compound with the molecular formula . It is the ''ortho'' isomer of the three isomeric benzenediols. This colorless compound occurs naturally in trace amounts. It was first discovered by destructive distillation of the plant extract catechin. About 20,000 tonnes of catechol are now synthetically produced annually as a commodity organic chemical, mainly as a precursor to pesticides, flavors, and fragrances. Catechol occurs as feathery white crystals that are very rapidly soluble in water. Isolation and synthesis Catechol was first isolated in 1839 by Edgar Hugo Emil Reinsch (1809–1884) by distilling it from the solid tannic preparation catechin, which is the residuum of catechu, the boiled or concentrated juice of ''Mimosa catechu'' (''Acacia catechu''). Upon heating catechin above its decomposition point, a substance that Reinsch first named ''Brenz-Katechusäure'' (burned catechu acid) ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
