Dihydrogossypetin
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IUPAC name (2R,3R)-3,3′,4′,5,7,8-Hexahydroxyflavan-4-one | |
Systematic IUPAC name (2R,3R)-2-(3,4-Dihydroxyphenyl)-3,5,7,8-tetrahydroxy-2,3-dihydro-4H-1-benzopyran-4-one | |
Other names 2,3-Dihydrogossypetin 3′,4′,5,7,8-pentahydroxyflavanonol | |
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Properties | |
Chemical formula | C15H12O8 |
Molar mass | 320.25 g/mol |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). N verify (what is YN ?) Infobox references |
Chemical compound
Dihydrogossypetin is a flavanonol, a type of flavonoid.[1]
Biosynthesis
The enzyme Taxifolin 8-monooxygenase hydroxylates taxifolin using NADH, NADPH, H+, and O2 to produce 2,3-dihydrogossypetin, NAD+, NADP+, and H2O.
References
- ^ Jeffrey, A. M.; Jerina, D. M.; Self, R.; Evans, W. C. (1972). "The bacterial degradation of flavonoids. Oxidative fission of the A-ring of dihydrogossypetin by a Pseudomonas sp". The Biochemical Journal. 130 (2): 383–90. doi:10.1042/bj1300383. PMC 1174417. PMID 4198081.
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Flavanonols and their glycosides
- Ampelopsin (Dihydromyricetin)
- Aromadedrin (Dihydrokaempferol)
- Dihydrogossypetin
- Dihydromorin
- Fustin (Dihydrofisetin)
- Garbanzol
- Pinobanksin
- Taxifolin (Dihydroquercetin)
- Lecontin
- (+)-fustin glucoside
- Astilbin
- Chrysandroside A
- Chrysandroside B
- Engeletin
- Eucryphin
- Smitilbin (Isoastilbin B)
- Xeractinol
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