Isovitexin
Compound with spectra: 5 NMR, and 1 MS (GC)
| SpectraBase Compound ID | KWYyLW8Uh6B |
|---|---|
| InChI | InChI=1S/C21H20O10/c22-7-14-17(26)19(28)20(29)21(31-14)16-11(25)6-13-15(18(16)27)10(24)5-12(30-13)8-1-3-9(23)4-2-8/h1-6,14,17,19-23,25-29H,7H2/t14-,17-,19+,20-,21+/m1/s1 |
| InChIKey | MYXNWGACZJSMBT-VJXVFPJBSA-N |
| Mol Weight | 432.38 g/mol |
| Molecular Formula | C21H20O10 |
| Exact Mass | 432.105647 g/mol |
| Enantiomer InChIKey | MYXNWGACZJSMBT-UBFQGWSASA-N |
| Copyright | Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved. |
|---|---|
| Source of Spectrum | CD-326-0-0 |
| 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:D2O |
| 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 | CD3OD |
- Saponaretin
4'-METHOXYLUTEOLIN-6-C-BETA-D-GLUCOPYRANOSIDE
APIGENIN-6-C-BETA-FUCOPYRANOSIDE
LUTEOLIN-6-C-FUCOPYRANOSIDE
5-HYDROXY-7-METHOXY-6-C-GLYCOSYLFLAVONE
6-C-ALPHA-L-ARABINOPYRANOSYLGLUTEOLIN
RUMPDXAYEFINQA-VRXCSTGVSA-N
4H-1-Benzopyran-4-one, 8-.beta.-D-glucopyranosyl-5,7-dihydroxy-2-(4-methoxyphenyl)-
RHAMNELLAFLAVOSIDE-C;6-C-BETA-D-4-EPIOLIOSYL-4''-O-BETA-D-GLUCOPYRANOSYL-APIGENIN
RHAMNELLAFLAVOSIDE-B;6-C-BETA-D-BOIVINOPYRANOSYL-4'-O-BETA-D-GLUCOPYRANOSYL-APIGENIN
| Title | Journal or Book | Year |
|---|---|---|
| Antiseptic Activity and Phenolic Constituents of the Aerial Parts of Vitex negundo var. cannabifolia | Molecules | 2010 |
| Chemical Constituents from the Leaves of <I>Lophatherum gracile</I> | Chinese Journal of Natural Medicines | 2010 |
| Quantitation of Chafurosides A and B in Tea Leaves and Isolation of Prechafurosides A and B from Oolong Tea Leaves | Journal of Agricultural and Food Chemistry | 2009 |
| Neural cell protective compounds isolated from Phoenix hanceana var. formosana | Phytochemistry | 2009 |
This compound is available in the following databases:
KnowItAll NMR Spectral Library
Author: Wiley
The KnowItAll NMR Spectral Library offers a comprehensive collection of NMR reference spectra, including NMR, CNMR, and XNMR, and covers a wide range of compounds including organics, polymers, monomers, metabolites, and more. Learn more.
KnowItAll Mass Spectral Library
Author: Wiley
The KnowItAll Mass Spectral Library offers a comprehensive collection of mass spectra, including the renowned Wiley Registry, and access to a wide range of compounds including pure organics, drugs, steroids, additives, geochemicals, petrochemicals, biomarkers, and more. Learn more.