KAEMPFEROL-3-O-SOPHOROSIDE-7-O-GLUCOSIDE
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Drawn and modelled with RDKit, 3D viewer 3Dmol.js. PubChem CID 44258829
Name
KAEMPFEROL-3-O-SOPHOROSIDE-7-O-GLUCOSIDE
IUPAC name
3-(((2S,5S)-4,5-dihydroxy-6-(hydroxymethyl)-3-(((2S,3R,5S)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl)oxy)tetrahydro-2H-pyran-2-yl)oxy)-5-hydroxy-2-(4-hydroxyphenyl)-7-(((2S,4S,5S)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl)oxy)-4H-chromen-4-one
SMILES
C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O[C@H]4C([C@H]([C@@H](C(O4)CO)O)O)O)O)O[C@H]5C(C([C@@H](C(O5)CO)O)O)O[C@H]6[C@@H](C([C@@H](C(O6)CO)O)O)O)O
Molecular formula
C33H40O21
Molecular weight
772.66 g/mol
Monoisotopic mass
772.2062 Da
Chemical classification: NPClassifier (Kim et al., 2021)
| Plant | Plant part | Amount | Reference |
|---|---|---|---|
| Equisetum arvense L. | aerial parts | - |
Jim Duke's personal files.
|
| Equisetum ramosissimum Desf. | - | - |
Saleh, N.A.M., Abdalla, M.F. (1980). The flavonoids of Equisetum ramosissimum. Phytochemistry, 19, 987 doi:10.1016/0031-9422(80)85161-2
|
| Equisetum telmateia Ehrh. | aerial parts | - |
Veit, M., Beckert, C., Hohne, C., Bauer, K., Geiger, H. (1995). Interspecific and intraspecific variation of phenolics in the genus Equisetum subgenus Equisetum. Phytochemistry, 38(4), 881-891 doi:10.1016/0031-9422(94)00658-g
|
| Lathyrus latifolius L. | leaf | - |
Ranabahu, P., Harborne, J.B. (1993). The flavonoids of the genus Lathyrus and a comparison of flavonoid patterns within the tribe Vicieae. Biochem Syst Ecol 21 (6/7) 715-722 doi:10.1016/0305-1978(93)90077-5
|
| Mutarda arvensis (L.) D.A.German | leaf | - |
Durkee, A.B., Harrbone, J.B. (1973). Flavonol glycosides in Brassica and Sinapis. Phytochemistry, 12, 1085-1089 doi:10.1016/0031-9422(73)85020-4
|