FL4D1AGS0002

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{{Metabolite
 
{{Metabolite
|SysName=3-hydroxy-2-(4-methoxyphenyl)-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxymethyl]oxan-2-yl]oxychroman-4-one
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|SysName=3-hydroxy-2- (4-methoxyphenyl) -7- [ (2S,3R,4S,5S,6R) -3,4,5-trihydroxy-6- [ [ (2S,3R,4S,5R) -3,4,5-trihydroxyoxan-2-yl ] oxymethyl ] oxan-2-yl ] oxychroman-4-one
|Common Name=&&Kushenol J&&3-hydroxy-2-(4-methoxyphenyl)-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxymethyl]oxan-2-yl]oxychroman-4-one&&
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|Common Name=&&Kushenol J&&3-hydroxy-2- (4-methoxyphenyl) -7- [ (2S,3R,4S,5S,6R) -3,4,5-trihydroxy-6- [ [ (2S,3R,4S,5R) -3,4,5-trihydroxyoxan-2-yl ] oxymethyl ] oxan-2-yl ] oxychroman-4-one&&
 
|CAS=101236-48-0
 
|CAS=101236-48-0
 
|KNApSAcK=C00008668
 
|KNApSAcK=C00008668
 
}}
 
}}

Latest revision as of 09:00, 22 September 2008


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Upper classes : FL Flavonoid : FL4 Dihydroflavonol :  FL4D1A Garbanzol and O-methyl derivatives (5 pages) :  FL4D1AGS O-Glycoside (1 pages)



Kushenol J
FL4D1AGS0002.png
Structural Information
Systematic Name 3-hydroxy-2- (4-methoxyphenyl) -7- [ (2S,3R,4S,5S,6R) -3,4,5-trihydroxy-6- [ [ (2S,3R,4S,5R) -3,4,5-trihydroxyoxan-2-yl ] oxymethyl ] oxan-2-yl ] oxychroman-4-one
Common Name
  • Kushenol J
  • 3-hydroxy-2- (4-methoxyphenyl) -7- [ (2S,3R,4S,5S,6R) -3,4,5-trihydroxy-6- [ [ (2S,3R,4S,5R) -3,4,5-trihydroxyoxan-2-yl ] oxymethyl ] oxan-2-yl ] oxychroman-4-one
Symbol
Formula C27H32O14
Exact Mass 580.179205732
Average Mass 580.53458
SMILES C(C(C(O)2)OC(Oc(c3)cc(O4)c(C(C(C4c(c5)ccc(c5)OC)O)=O)c3)C(C2O)O)OC(O1)C(O)C(C(O)C1)O
Physicochemical Information
Melting Point
Boiling Point
Density
Optical Rotation
Reflactive Index
Solubility
Spectral Information
Mass Spectra
UV Spectra
IR Spectra
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Chromatograms



Species Information

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