(+)-MELILOTOCARPAN_A
Compound with spectra: 1 NMR
| SpectraBase Compound ID | shI4XuqVb3 |
|---|---|
| InChI | InChI=1S/C17H16O5/c1-19-9-3-4-10-12-8-21-17-11(16(12)22-14(10)7-9)5-6-13(20-2)15(17)18/h3-7,12,16,18H,8H2,1-2H3/t12-,16-/m0/s1 |
| InChIKey | YHSXPHNOIMTWTH-LRDDRELGSA-N |
| Mol Weight | 300.31 g/mol |
| Molecular Formula | C17H16O5 |
| Exact Mass | 300.099774 g/mol |
| Enantiomer InChIKey | YHSXPHNOIMTWTH-MLGOLLRUSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
MELILOTOCARPAN-B
2-HYDROXY-4,9-DIMETHOXYPTEROCARPIN
3,8,9-Trimethoxypterocarpan
SECUNDIFLOROL-I;3-HYDROXY-8,9-DIMETHOXYPTEROCARPAN
ERYTHRACANTHA-B;3,9-DIHYDROXY-8-(GAMMA,GAMMA-DIMETHYLALLYL)-PTEROCARPAN
CALOPOCARPIN;3,9-DIHYDROXYPTEROCARPAN-2-(3-METHYLBUT-2-ENYL)
CALOPOCARPIN
LESPEDEZOL-D1
Lawsonicin - triacetate
(6aR,11aR)-6a-deuterio-6,11a-dihydrobenzofuro[3,2-c]chromene
| Title | Journal or Book | Year |
|---|---|---|
| Metabolites of the “Smoke Tree”, Dalea spinosa, Potentiate Antibiotic Activity against Multidrug-Resistant Staphylococcus aureus | Journal of Natural Products | 2006 |