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CALYCOSIN
SpectraBase Compound ID GE29DypXAfY
InChI InChI=1S/C16H12O5/c1-20-14-5-2-9(6-13(14)18)12-8-21-15-7-10(17)3-4-11(15)16(12)19/h2-8,17-18H,1H3
InChIKey ZZAJQOPSWWVMBI-UHFFFAOYSA-N
Mol Weight 284.27 g/mol
Molecular Formula C16H12O5
Exact Mass 284.068473 g/mol
Copyright Copyright © 2002-2024 Wiley-VCH Verlag GmbH & Co. KGaA. All Rights Reserved.
Solvent C2D6SO dimethylsulfo
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.
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 DMSO-D6
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 DMSO-D6
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum G-55-1265-X
  • CALYOSIN
  • CALYCOSIN;7,3'-DIHYDROXY-4'-METHOXY-ISOFLAVONE
  • CALYCOSIN;M12
  • 7,3'-Dihydroxy-4'-methoxyisoflavone
Title Journal or Book Year
Profiling and identification of the metabolites of calycosin in rat hepatic 9000×g supernatant incubation system and the metabolites of calycosin-7-O-β-d-glucoside in rat urine by HPLC–DAD–ESI-IT-TOF-MSn technique Journal of Pharmaceutical and Biomedical Analysis 2012
Isolation, identification and antiviral activities of metabolites of calycosin-7-O-β-d-glucopyranoside Journal of Pharmaceutical and Biomedical Analysis 2011
New isoflavonolignan with quinone reductase inducing activity from Alhagi pseudalhagi (M.B.) Fitoterapia 2010
Solvent effect in1H NMR spectra of 3′-hydroxy-4′-methoxy isoflavonoids fromAstragalus membranaceus var.mongholicus Magnetic Resonance in Chemistry 2006
An isoflavan-quinone and a flavonol from Millettia laurentii1Part 10 in the series “The Millettia of Cameroon”.1 Phytochemistry 1999

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