ISOIMPERATORIN
Compound with spectra: 7 NMR, and 4 MS (GC)
| SpectraBase Compound ID | HTSACuQSgW9 |
|---|---|
| InChI | InChI=1S/C16H14O4/c1-10(2)5-7-19-16-11-3-4-15(17)20-14(11)9-13-12(16)6-8-18-13/h3-6,8-9H,7H2,1-2H3 |
| InChIKey | IGWDEVSBEKYORK-UHFFFAOYSA-N |
| Mol Weight | 270.28 g/mol |
| Molecular Formula | C16H14O4 |
| Exact Mass | 270.089209 g/mol |
| Copyright | Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved. |
|---|---|
| Source of Spectrum | CD-362-0-0 |
| Copyright | Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved. |
|---|---|
| Source of Spectrum | TA-0-1094-7 |
| Copyright | Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved. |
|---|---|
| Source of Spectrum | Y4-77-360-0 |
| Copyright | Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved. |
|---|---|
| Source of Spectrum | Va-0-0-0 |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
| 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 | CDCl3 |
- 7H-Furo[3,2-g][1]benzopyran-7-one, 4-[(3-methyl-2-butenyl)oxy]-
Bergamottin
4-(3-Cyanopropoxy)-7H-furo[3,2-g][1]benzopyran-7-one
4-(4-Pentynyloxy)-7H-furo[3,2-g][1]benzopyran-7-one
4-(3-Phenoxypropoxy)-7H-furo[3,2-g][1]benzopyran-7-one
4-(3-Benzyloxypropoxy)-7H-furo[3,2-g][1]benzopyran-7-one
4-(4-[4-Methylphenoxy]butoxy)-7H-furo[3,2-g][1]benzopyran-7-one
4-[5-(3,5-Dimethoxyphenoxy)pentoxy]-7H-furo[3,2-g][1]benzopyran-7-one
4-[3-(3,5-Dimethoxyphenoxy)propoxy]-7H-furo[3,2-g][1]benzopyran-7-one
4-[5-(4-Methylphenoxy)pentoxy]-7H-furo[3,2-g][1]benzopyran-7-one
4-(4-[4-Chlorphenoxy]butoxy)-7H-furo[3,2-g][1]benzopyran-7-one
| Title | Journal or Book | Year |
|---|---|---|
| Antioxidant, 5-Lipoxygenase Inhibitory and Cytotoxic Activities of Compounds Isolated from the Ferula lutea Flowers | Molecules | 2014 |
| Cytotoxic Constituents from the Stems of Clausena lansium (Lour.) Skeels | Molecules | 2013 |
| Chromatographic fingerprint analysis and characterization of furocoumarins in the roots of Angelica dahurica by HPLC/DAD/ESI-MSn technique | Journal of Pharmaceutical and Biomedical Analysis | 2008 |
| Antiproliferative Constituents from Umbelliferae Plants. V. A New Furanocoumarin and Falcarindiol Furanocoumarin Ethers from the Root of Angelica japonica. | Chemical and Pharmaceutical Bulletin | 1999 |
| Furanocoumarins with affinity to brain benzodiazepine receptors in vitro | Phytochemistry | 1997 |
| Steroids, chromone and coumarins from angelica officinalis | Phytochemistry | 1984 |
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