PEUUVVGQIVMSAW-RZTYQLBFSA-N
Compound with spectra: 6 NMR, 1 FTIR, and 1 MS (GC)
| SpectraBase Compound ID | AyX0fW8wJPQ |
|---|---|
| InChI | InChI=1S/C22H26O6/c1-23-17-7-5-13(9-19(17)25-3)21-15-11-28-22(16(15)12-27-21)14-6-8-18(24-2)20(10-14)26-4/h5-10,15-16,21-22H,11-12H2,1-4H3/t15-,16-,21+,22+/m0/s1 |
| InChIKey | PEUUVVGQIVMSAW-RZTYQLBFSA-N |
| Mol Weight | 386.44 g/mol |
| Molecular Formula | C22H26O6 |
| Exact Mass | 386.172939 g/mol |
| Enantiomer InChIKey | PEUUVVGQIVMSAW-DJDZNOHASA-N |
| Copyright | Copyright © 2024-2025 John Wiley & Sons, Inc. All Rights Reserved. |
|---|
| Copyright | Copyright © 2020-2025 John Wiley & Sons, Inc. All Rights Reserved. |
|---|---|
| Source of Spectrum | D9-20-1117-18 |
| Copyright | Copyright © 2016-2025 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
| Copyright | Copyright © 2016-2025 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
| Copyright | Copyright © 2016-2025 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
| Copyright | Copyright © 2016-2025 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|
| Copyright | Copyright © 2016-2025 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
| Copyright | Copyright © 2016-2025 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | ACETONE-D6 |
- (REL)-(7S,7'S,8R,8'R)-EUDESMIN
- EUDESMIN;REL-(7S,8R,7'S,8'R)-3,4,3',4'-TETRAMETHOXY-DELTA(1,3,5,1',3',5')-8.8',9.O.7',7.O.9'-LIGNAN
- (+)-Eudesmin
- Eudesmin
(+)-DEMETHOXYPINORESINOL;(1R*,2S*,5R*,6S*)-2-(4'-HYDROXYPHENYL)-6-(3''-METHOXY-4''-HYDROXYPHENYL)-3,7-DIOXABICYCLO-[3.3.0]-OCTANE
(-)-EPI-(4-HYDROXYPHENYLGUAIACYL)TETRAHYDROFUROFURAN LIGNAN , (-)-(1S,2S,5S,6R)-2-(4-HYDROXYPHENYL)-6-(3-METHOXY-4-HYDROXYPHENYL)-3,7-DIOXABICYCLO[3.3.0]OCTANE
#1;(-)-EPI-(4-HYDROXYPHENYL-GUAIACYL)-TETRAHYDROFURAN-LIGNAN;(1S,2S,5S,6R)-2-(4-HYDROXYPHENYL)-6-(3-METHOXY-4-HYDROXYPHENYL)-3,7-DIOXABICYCLO-[3.3.O]-OCTANE
DE-4'-O-METHYLYANGABIN
Syringaresinol, di-TMS
(2sr,3rs,4rs)-2-(1,3-Benzodioxol-5-yl)-3-methoxymethoxymethyltetrahydrofuran-4-methanol
BMCOXLYYHXMSLA-BLIXFSHQSA-N
(2SR,3RS,4SR)-4-ACETOXYMETHYL-2-(1,3-BENZODIOXOL-5-YL)-TETRAHYDROFURAN-3-METHANOL
4-[5-(4-Hydroxy-3,5-dimethoxyphenyl)-3,4-bis(hydroxymethyl)oxolan-2-yl]-2,6-dimethoxyphenol. tetramethyl ether
FUTOKADSURIN-C;REL-(7R,8R,7'S,8'S)-3',4'-DIMETHOXY-3,4-METHYLENEDIOXY-7,7'-EPOXYLIGNAN
| Title | Journal or Book | Year |
|---|---|---|
| Lignans and Other Constituents from Aerial Parts of Haplophyllum Villosum | Molecules | 2011 |
| Aromatic compounds from three Brazilian Lauraceae species | Química Nova | 2010 |
| Biological activities of lignoids from Amazon Myristicaceae species: Virola michelii, V. mollissima, V. pavonis and Iryanthera juruensis | Journal of the Brazilian Chemical Society | 2009 |
| Lignans from the roots of Echinops giganteus | Phytochemistry | 2004 |
| Biotransformation of lignans: Metabolism of (+)-eudesmin and (+)-magnolin in Spodoptera litura | Phytochemistry | 1995 |
| Biotransformation of lignans: a specific microbial oxidation of (+)-eudesmin and (+)-magnolin by Aspergillus niger | Phytochemistry | 1993 |
This compound is available in the following databases:
KnowItAll NMR Spectral Library
Author: Wiley
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KnowItAll Mass Spectral Library
Author: Wiley
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