ASPERULOSIDIC ACID-DEACETYL-METHYL ESTER
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Drawn and modelled with RDKit, 3D viewer 3Dmol.js. PubChem CID 6325021
Name
ASPERULOSIDIC ACID-DEACETYL-METHYL ESTER
IUPAC name
methyl (1S,4aS,5S,7aS)-5-hydroxy-7-(hydroxymethyl)-1-(((2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl)oxy)-1,4a,5,7a-tetrahydrocyclopenta[c]pyran-4-carboxylate
SMILES
COC(=O)C1=CO[C@H]([C@H]2[C@@H]1[C@H](C=C2CO)O)O[C@H]3[C@@H]([C@H]([C@@H]([C@H](O3)CO)O)O)O
Molecular formula
C17H24O11
Molecular weight
404.37 g/mol
Monoisotopic mass
404.1319 Da
Chemical classification: NPClassifier (Kim et al., 2021)
| Plant | Plant part | Amount | Reference |
|---|---|---|---|
| Cruciata laevipes Opiz | aerial parts | - |
Mitova, M.I., Anchev, M.E., Panev, S.G., Handjieva, N.V., Popov, S.S. (1996). Coumarins and iridoids from Crucianella graeca, Gruciata glabra, Cruciata laevipes and Curciata pedemontana (Rubiaceae). Z Naturforsch Ser C, 51(1/10), 631-634 doi:10.1515/znc-1996-9-1005
|
| Galium album Mill. | - | - |
Chervenkova, K., Nikolovadamyanova, B. (2000). The elution pattern of iridoid glucosides from Galium species on c-18 reversed-phase high performance liquid chromatography. J Liq Chrom Rel Technol, 23(5), 741-753 doi:10.1081/jlc-100101486
|
| Plantago lanceolata L. | aerial parts | - |
Handjieva, N., Saadi, H., Evstatieva, L. (1991). Iridoid glucosides from Plantago altissima L., Plantago lanceolata L., Plantago atrata Hoppe and Plantago argentea Chaix. Z Naturforsch Ser C, 46(9/10), 963-965 doi:10.1515/znc-1991-9-1041
|