ISORHAMNETIN-3-RUTINOSIDE-7-RHAMNOSIDE
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Drawn and modelled with RDKit, 3D viewer 3Dmol.js. PubChem CID 44259176
Name
ISORHAMNETIN-3-RUTINOSIDE-7-RHAMNOSIDE
IUPAC name
2-(3,4-dihydroxyphenyl)-5-hydroxy-3-(((2S,5S)-3,4,5-trihydroxy-6-((((2R,4S,5R)-3,4,5-trihydroxy-6-methyltetrahydro-2H-pyran-2-yl)oxy)methyl)tetrahydro-2H-pyran-2-yl)oxy)-7-(((2S,4S,5R)-3,4,5-trihydroxy-6-methyltetrahydro-2H-pyran-2-yl)oxy)-4H-chromen-4-one
SMILES
CC1[C@@H]([C@@H](C([C@@H](O1)OCC2[C@H](C(C([C@@H](O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O[C@H]5C([C@H]([C@H](C(O5)C)O)O)O)C6=CC(=C(C=C6)O)O)O)O)O)O)O)O
Molecular formula
C33H40O20
Molecular weight
756.66 g/mol
Monoisotopic mass
756.2113 Da
Chemical classification: NPClassifier (Kim et al., 2021)
| Plant | Plant part | Amount | Reference |
|---|---|---|---|
| Typha latifolia L. | - | - |
Kosuge, T., Ishida, K., Ito, Y., Kato, H. (1989). Isorhamnetin derivatives from a reed mace (Typha lactifolia) as hemostatics. Patent Japan Kokai Tokkyo Koho 01 213,294
|
| Typha latifolia L. | pollen | - |
Ishida, H., Umino, T., Tsuji, K., Kosuge, T. (1988). Studies on the antihemorrhagic substances in herbs classified as hemostatics in chinese medicine. ix. on the antihemorrhagic principles in Typha lactifolia L. Chem Pharm Bull, 36(11), 4414-4420 doi:10.1248/cpb.36.4414
|