7-METHOXY-5,6,4'-TRIHYDROXYISOFLAVONE
Compound with spectra: 3 NMR
| SpectraBase Compound ID | GdHLPkBASiq |
|---|---|
| InChI | InChI=1S/C16H12O6/c1-21-12-6-11-13(16(20)15(12)19)14(18)10(7-22-11)8-2-4-9(17)5-3-8/h2-7,17,19-20H,1H3 |
| InChIKey | PVUYNAPZRICYPA-UHFFFAOYSA-N |
| Mol Weight | 300.27 g/mol |
| Molecular Formula | C16H12O6 |
| Exact Mass | 300.063388 g/mol |
| 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 |
- 4',5,6-TRIHYDROXY-7-METHOXYISOFLAVONE
5,6-DIHYDROXY-4',7-DIMETHOXYISOFLAVONE
IRISOLIDONE
TTR;TECTORIGENIN
5-HYDROXY-7-O-[3-(1-C-4-O-ACETYL-2,3,6-TRIDEOXY-BETA-L-ERYTHRO-HEX-2-EN-PYRANOSYL)-PROPYL]-3-(4'-HYDROXYPHENYL)-CHROMEN-4-ONE
5-HYDROXY-7-O-[3-(1-C-4-O-ACETYL-2,3,6-TRIDEOXY-ALPHA-L-ERYTHRO-HEX-2-EN-PYRANOSYL)-PROPYL]-3-(4'-HYDROXYPHENYL)-CHROMEN-4-ONE
5-HYDROXY-7,3',4'-TRIMETHOXYISOFLAVONE
GENISTEIN-7-ACETYLFERULIC-ACID
5-HYDROXY-7-O-[5-(1-C-4-O-ACETYL-2,3,6-TRIDEOXY-BETA-L-ERYTHRO-HEX-2-EN-PYRANOSYL)-PENTYL]-3-(4'-HYDROXYPHENYL)-CHROMEN-4-ONE
5-HYDROXY-7-O-[5-(1-C-4-O-ACETYL-2,3,6-TRIDEOXY-ALPHA-L-ERYTHRO-HEX-2-EN-PYRANOSYL)-PENTYL]-3-(4'-HYDROXYPHENYL)-CHROMEN-4-ONE
5-HYDROXY-7-O-[4-(1-C-4-O-ACETYL-2,3,6-TRIDEOXY-BETA-L-ERYTHRO-HEX-2-EN-PYRANOSYL)-BUTYL]-3-(4'-HYDROXYPHENYL)-CHROMEN-4-ONE
| Title | Journal or Book | Year |
|---|---|---|
| Chemical Constituents of the Ethyl Acetate Extract of Belamcanda chinensis (L.) DC Roots and Their Antitumor Activities | Molecules | 2012 |
| Studies of the Selective O-Alkylation and Dealkylation of Flavonoids.XX. A Convenient Method for Synthesizing 5,6,7-Trihydroxyisoflavones and 5,6-Dihydroxy-7-methoxyisoflavones. | Chemical and Pharmaceutical Bulletin | 1996 |
| Isoflavones, a sesquiterpene lactone-monoterpene adduct and other constituents of Gaillardia species | Phytochemistry | 1991 |
This compound is available in the following databases:
KnowItAll NMR Spectral Library
Author: Wiley
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