9-HYDROXY-1-METHOXY-8-(3-HYDROXY-3-METHYLBUTYL)-6',6'-DIMETHYL-4',5-DIHYDRO-[6-H]-PYRANO-[2'.3':3.2]-PTEROCARPAN
Compound with spectra: 1 NMR
![9-HYDROXY-1-METHOXY-8-(3-HYDROXY-3-METHYLBUTYL)-6',6'-DIMETHYL-4',5-DIHYDRO-[6-H]-PYRANO-[2'.3':3.2]-PTEROCARPAN](/api/compound/I83Old7br8o.png?ph=true&h=300&w=458 "9-HYDROXY-1-METHOXY-8-(3-HYDROXY-3-METHYLBUTYL)-6',6'-DIMETHYL-4',5-DIHYDRO-[6-H]-PYRANO-[2'.3':3.2]-PTEROCARPAN")
| SpectraBase Compound ID | I83Old7br8o |
|---|---|
| InChI | InChI=1S/C26H32O6/c1-25(2,28)8-6-14-10-16-17-13-30-21-12-20-15(7-9-26(3,4)32-20)23(29-5)22(21)24(17)31-19(16)11-18(14)27/h10-12,17,24,27-28H,6-9,13H2,1-5H3/t17-,24+/m0/s1 |
| InChIKey | HNUJQUYWDAIHPF-BXKMTCNYSA-N |
| Mol Weight | 440.5 g/mol |
| Molecular Formula | C26H32O6 |
| Exact Mass | 440.219889 g/mol |
| Enantiomer InChIKey | HNUJQUYWDAIHPF-OSPHWJPCSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
1,2,7a,12a-Tetrahydro-9-hydroxy-3,3-dimethyl-10,13-dimethoxy-3H,7H-benzofuro[2',3':4,5]pyran[3,2-g][1]benzopyran
1,2,7a,12a-Tetrahydro-3,3-dimethyl-10,13-dimethoxy-3H,7H-benzofuro[2',3':4,5]pyran[3,2-g][1]benzopyran
3,4,8a,13a-Tetrahydro-2,2-dimethyl-5,11-dimethoxy-2H,8H-benzofuro[2',3':4,5]pyran[2,3-h][1]benzopyran
BOLUCARPAN_C
1-METHOXYERYTHRABYSSIN_II
BOLUCARPAN_D
10-Methoxy-3,3,7,7-tetramethyl-2,3,7a,12a-tetrahydro-1H,7H-[1]benzofuro[3,2-c]pyrano[3,2-g]chromen-9-ol
2H,6H-[1,3]Dioxolo[5,6]benzofuro[3,2-c]pyrano[2,3-h][1]benzopyran, 6a,12a-dihydro-2,2-dimethyl-, cis-(.+-.)-
LESPECYRTIN_E_5
ERYBrAEDIN-D
| Title | Journal or Book | Year |
|---|---|---|
| Isoflavonoids and Coumarins from Glycyrrhiza uralensis: Antibacterial Activity against Oral Pathogens and Conversion of Isoflavans into Isoflavan-Quinones during Purification | Journal of Natural Products | 2011 |