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(-)-EPICATECHIN-3-O-GALLATE
SpectraBase Compound ID G0wXYds5o4f
InChI InChI=1S/C22H18O10/c23-11-6-14(25)12-8-19(32-22(30)10-4-16(27)20(29)17(28)5-10)21(31-18(12)7-11)9-1-2-13(24)15(26)3-9/h1-7,19,21,23-29H,8H2/t19-,21-/m1/s1
InChIKey LSHVYAFMTMFKBA-TZIWHRDSSA-N
Mol Weight 442.38 g/mol
Molecular Formula C22H18O10
Exact Mass 442.089997 g/mol
Enantiomer InChIKey LSHVYAFMTMFKBA-FPOVZHCZSA-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.
Solvent CD3OD
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 CD3OD
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent DMSO-D6
  • (-)-EPICATECHIN-3-GALLATE
  • (-)-EPICATECHIN-3-O-GALLATE;(2R,3R)-5,7,3',4'-TETRAHYDROXY-FLAVAN-3-O-GALLATE
  • EPICATECHIN-3-O-GALLATE
Title Journal or Book Year
Separation of Polyphenols and Caffeine from the Acetone Extract of Fermented Tea Leaves (Camellia sinensis) Using High-Performance Countercurrent Chromatography Molecules 2015
Antioxidant Phenolic Compounds from Pu-erh Tea Molecules 2012
A new epicatechin gallate and calpain inhibitory activity from Orostachys japonicus Fitoterapia 2009
1H and13C NMR Assignments of Some Green Tea Polyphenols Magnetic Resonance in Chemistry 1996
Two phloroglucinol glucosides, flavan gallates and flavonol glycosides from Sedum sediforme flowers Phytochemistry 1993

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