DL-2,3-DIHYDRO-4-HYDROXY-7-METHYL-2-ISOPROPENYL-5H-FURO[3,2G] [1] BENZOPYRAN-5-ONE
Compound with spectra: 3 NMR
![DL-2,3-DIHYDRO-4-HYDROXY-7-METHYL-2-ISOPROPENYL-5H-FURO[3,2G] [1] BENZOPYRAN-5-ONE](/api/compound/BVLwjPLz2RJ.png?ph=true&h=300&w=458 "DL-2,3-DIHYDRO-4-HYDROXY-7-METHYL-2-ISOPROPENYL-5H-FURO[3,2G] [1] BENZOPYRAN-5-ONE")
| SpectraBase Compound ID | BVLwjPLz2RJ |
|---|---|
| InChI | InChI=1S/C15H14O4/c1-7(2)11-5-9-12(19-11)6-13-14(15(9)17)10(16)4-8(3)18-13/h4,6,11,17H,1,5H2,2-3H3 |
| InChIKey | VADRYAHZDJOAMG-UHFFFAOYSA-N |
| Mol Weight | 258.27 g/mol |
| Molecular Formula | C15H14O4 |
| Exact Mass | 258.089209 g/mol |
| Copyright | Copyright © 2002-2024 Wiley-VCH Verlag GmbH & Co. KGaA. All Rights Reserved. |
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| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
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| Solvent | CDCl3 |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CD3OD |
- HETEROCARPIN
CQ-8;CHAETOQUADRIN-H;5-HYDROXY-7-METHOXY-6-[(3',7'-EPOXY-2'-METHYL-5'-OXO)-3'-OCTENYL]-2-METHYL-CHROMONE
CQ-7;CHAETOQUADRIN-G;(2'R,7'S)-5-HYDROXY-7-METHOXY-6-[(3',7'-EPOXY-2'-METHYL-5'-OXO)-3'-OCTENYL]-2-METHYL-CHROMONE
2,8-DIMETHYL-5-HYDROXY-2-HYDROXYMETHYL-3,4-DIHYDRO-2H,3H-BENZO-[1,2-B:5,4-B']-DIPYRAN-6-ONE
PERFORATIN-F;5,7-DIMETHOXY-2-METHYL-8-(2-HYDROXY-3-METHYL-3-BUTENYL)-CHROMONE
PERFORATIN-D;5,7-DIMETHOXY-2-METHYL-8-(2,3-DIHYDROXY-3-METHYLBUTYL)-CHROMONE
GANCAONINO
2H,10H-Benzo[1,2-b:3,4-b']dipyran-10-one, 3,4-dihydro-5-hydroxy-2,2,8-trimethyl-
MDBCIIGAFMRLQN-UHFFFAOYSA-N
PERFORAMONE-A;5-HYDROXY-7-METHOXY-2-METHYL-8-(2,3-EPOXY-3-METHYLBUTYL)-CHROMONE
ARTOCARMIN_B;4''-TRANS-PARA-COUMAROYLARTOCARMIN_A
| Title | Journal or Book | Year |
|---|---|---|
| Anti-Inflammatory Activity of Heterocarpin from the Salt Marsh Plant Corydalis heterocarpa in LPS-Induced RAW 264.7 Macrophage Cells | Molecules | 2015 |
| Chromone glucosides from Cnidium japonicum | Phytochemistry | 1993 |