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ASTILBIN;DIHYDROQUERCETIN-3-O-ALPHA-L-RHAMNOPYRANOSIDE
SpectraBase Compound ID G8plWAMAfHL
InChI InChI=1S/C21H22O11/c1-7-15(26)17(28)18(29)21(30-7)32-20-16(27)14-12(25)5-9(22)6-13(14)31-19(20)8-2-3-10(23)11(24)4-8/h2-7,15,17-26,28-29H,1H3/t7-,15-,17+,18+,19+,20-,21-/m0/s1
InChIKey ZROGCCBNZBKLEL-MPRHSVQHSA-N
Mol Weight 450.4 g/mol
Molecular Formula C21H22O11
Exact Mass 450.116212 g/mol
Enantiomer InChIKey ZROGCCBNZBKLEL-HYLDYJRMSA-N
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent ACETONE-D6
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CD3OD
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent DMSO-D6
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent ACETONE-D6
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CD3OD
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent C5D5N
  • ASTILBIN;3,3',4',5,7-PENTAHYDROXY-FLAVANONE-3-O-[6-DEOXY-(ALPHA-L-MANNOPYRANODIDE)]
  • (+)-ASTILBIN
  • (-)-(2R,3R)-ASTILBIN;(-)-(2R,3R)-3-O-ALPHA-L-RHAMNOPYRANOSYL-5,7,3',4'-TETRAHYDROXYDIHYDROFLAVONOL
  • (REL)-(2R,3R)-ASTILBIN
  • ASTILBIN
Title Journal or Book Year
Aromatic compounds from three Brazilian Lauraceae species Química Nova 2010
Antioxidant and cytotoxic activities of 'açaí' (Euterpe precatoria Mart.) Química Nova 2008
Identification of a New Metabolite of Astilbin, 3′-O-Methylastilbin, and Its Immunosuppressive Activity against Contact Dermatitis Clinical Chemistry 2007
Isolation and in vitro antibacterial activity of astilbin, the bioactive flavanone from the leaves of Harungana madagascariensis Lam. ex Poir. (Hypericaceae) Journal of Ethnopharmacology 2006
6-C-formyl and 6-C-hydroxymethyl flavanones from Petiveria alliacea Phytochemistry 1992

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