KATSUMADAIN-A;SYNTHETIC
Compound with spectra: 3 NMR, and 1 MS (GC)
| SpectraBase Compound ID | DQNnjQRtPj9 |
|---|---|
| InChI | InChI=1S/C32H28O4/c33-26(18-16-23-10-4-1-5-11-23)20-28-21-29(25-14-8-3-9-15-25)31-30(35-28)22-27(36-32(31)34)19-17-24-12-6-2-7-13-24/h1-15,17,19,22,28-29H,16,18,20-21H2/b19-17+/t28-,29+/m1/s1 |
| InChIKey | IAIGBNIWSBFKNA-FIACUDKOSA-N |
| Mol Weight | 476.6 g/mol |
| Molecular Formula | C32H28O4 |
| Exact Mass | 476.198759 g/mol |
| Enantiomer InChIKey | IAIGBNIWSBFKNA-OQYGYJIPSA-N |
| Copyright | Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved. |
|---|---|
| Source of Spectrum | G4-62-1673-1 |
| 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 |
- KATSUMADAIN-A;NATURAL
- KATSUMADAIN_A
- Katsumadain A
2-Amino-7-methyl-5-oxo-4-phenyl-4H,5H-pyrano[4,3-b]pyran-3-carbonitrile
5-[(4-Hydroxy-6-methyl-2-oxo-2H-pyran-3-yl)(4-(trifluoromethyl)phenyl)methyl]-1,3-dimethylpyrimidine-2,4,6(1H,3H,5H)-trione
Warfarin-M (dihydro-) ET
5-[(4-Bromophenyl)(4-hydroxy-6-methyl-2-oxo-2H-pyran-3-yl)methyl]-1,3-dimethylpyrimidine-2,4,6(1H,3H,5H)-trione
trans-4-Carbethoxy-2,3-dihydro-2-fur-2'-oyl-5-methyl-3-(4-methylphenyl)furan
Methyl 3-(3-acetoxy-5-methoxy-1,2-benzoquinone-4-yl)-3-phenylpropionate
5-[(4-Hydroxy-6-methyl-2-oxo-2H-pyran-3-yl)(phenyl)methyl]-1,3-dimethylpyrimidine-2,4,6(1H,3H,5H)-trione
trans-4-Carbethoxy-2,3-dihydro-2-fur-2'-oyl-5-methyl-3-phenylfuran
Ethyl 5-cyano-2-methyl-4-phenyl-6-(1H-pyrrol-1-yl)-4H-pyran-3-carboxylate
4H-pyran-3-carboxylic acid, 6-amino-4-(2-chlorophenyl)-5-cyano-2-methyl-, 2-propenyl ester
| Title | Journal or Book | Year |
|---|---|---|
| Bioinspired total synthesis of katsumadain A by organocatalytic enantioselective 1,4-conjugate addition | Beilstein Journal of Organic Chemistry | 2013 |
| Antiviral Potential and Molecular Insight into Neuraminidase Inhibiting Diarylheptanoids from Alpinia katsumadai | Journal of Medicinal Chemistry | 2009 |
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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