Methyl dichloroasterrate
Compound with spectra: 2 NMR, and 1 MS (GC)
| SpectraBase Compound ID | A4ZdJzcKTFx |
|---|---|
| InChI | InChI=1S/C18H16Cl2O8/c1-7-12(19)14(22)11(18(24)27-4)16(13(7)20)28-15-9(17(23)26-3)5-8(21)6-10(15)25-2/h5-6,21-22H,1-4H3 |
| InChIKey | UWTOESDPWKUNBD-UHFFFAOYSA-N |
| Mol Weight | 431.22 g/mol |
| Molecular Formula | C18H16Cl2O8 |
| Exact Mass | 430.022223 g/mol |
| Copyright | Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved. |
|---|---|
| Source of Spectrum | G4-65-9-5 |
| 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 | DMSO-D6 |
- METHYL-3,5-DICHLOROASTERRIC-ACID
GEOMYCIN_A
Pestalotether A
11H-Dibenzo[b,e][1,4]dioxepin-11-one, 3,8-dihydroxy-1,4,6-trimethyl-
9H-Xanthen-9-one, 2,4-dichloro-1,3,6-trihydroxy-8-methyl-
1,7-DIHYDROXY-5,6-DIMETHOXY-XANTHONE
BUELLIN
2,4,5,7-Tetrachloro-8-methyl-1,3,6-trihydroxy-xanthone
Ethanone, 1-[3-(2-acetyl-3-hydroxy-5-methoxy-4-methylphenoxy)-2,4,6-trimethoxy- 5-methylphenyl]-
DRIMIOPSIN-E;3,6,8-TRIHYDROXY-6-METHOXY-1-METHYLXANTHONE
1,3,8-TRIHYDROXY-5,7-DIMETHOXYXANTHONE
| Title | Journal or Book | Year |
|---|---|---|
| Fungal Metabolites, Asterric Acid Derivatives Inhibit Vascular Endothelial Growth Factor (VEGF)-induced Tube Formation of HUVECs. | The Journal of Antibiotics | 2002 |
| New Chlorinated Diphenyl Ethers from an Aspergillus Species | Journal of Natural Products | 2001 |
This compound is available in the following databases:
Wiley Registry of Mass Spectral Data 2023
Author: Wiley
The foundation library for any analytical laboratory running mass spectrometry, the Wiley Registry provides the broadest coverage available in any mass spectral library Learn more.