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
Compound with spectra: 1 NMR
![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](/api/compound/Kk86J4iRLk0.png?ph=true&h=300&w=458 "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")
| SpectraBase Compound ID | Kk86J4iRLk0 |
|---|---|
| InChI | InChI=1S/C28H30O8/c1-17-25(36-18(2)29)12-11-21(35-17)6-4-3-5-13-33-22-14-24(31)27-26(15-22)34-16-23(28(27)32)19-7-9-20(30)10-8-19/h7-12,14-17,21,25,30-31H,3-6,13H2,1-2H3/t17-,21-,25+/m0/s1 |
| InChIKey | JMTWGHFVKVEUST-SBJAYZTMSA-N |
| Mol Weight | 494.54 g/mol |
| Molecular Formula | C28H30O8 |
| Exact Mass | 494.194068 g/mol |
| Enantiomer InChIKey | JMTWGHFVKVEUST-ZIYZLLSTSA-N |
| Copyright | Copyright © 2016-2025 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
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
5-HYDROXY-7-O-[4-(1-C-4-O-ACETYL-2,3,6-TRIDEOXY-ALPHA-L-ERYTHRO-HEX-2-EN-PYRANOSYL)-BUTYL]-3-(4'-HYDROXYPHENYL)-CHROMEN-4-ONE
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
Biochanin A, heptafluorobutyryl ether
OROBOL-7,3'-DIMETHYLETHER
5-HYDROXY-7,3',4'-TRIMETHOXYISOFLAVONE
3'-FORMYL-5,4'-DIHYDROXY-7-METHOXYISOFLAVONE
GENISTEIN-4'-O-ALPHA-L-RHAMNOPYRANOSIDE
| Title | Journal or Book | Year |
|---|---|---|
| Synthesis and Cytotoxicity of 2,3-Enopyranosyl C-Linked Conjugates of Genistein | Molecules | 2014 |