For research use only. Not for therapeutic Use.
Rutin is a natural flavonol glycoside with iron chelating and antioxidant properties. At least in part due to these actions, rutin has diverse actions at cellular and physiological levels, demonstrating anti-inflammatory, anti-cancer, and anti-fibrosis effects in animal models. Rutin also displays hepato- and neuroprotective actions in animal models.
| Catalog Number | R066644 |
| CAS Number | 250249-75-3 |
| Synonyms | Quercetin-3-O-rutinoside;Rutoside;Sophorin |
| Molecular Formula | C27H36O19 |
| Purity | ≥95% |
| Target | Metabolic Enzyme/Protease |
| Storage | Room temperature |
| IUPAC Name | 2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one;trihydrate |
| InChI | InChI=1S/C27H30O16.3H2O/c1-8-17(32)20(35)22(37)26(40-8)39-7-15-18(33)21(36)23(38)27(42-15)43-25-19(34)16-13(31)5-10(28)6-14(16)41-24(25)9-2-3-11(29)12(30)4-9;;;/h2-6,8,15,17-18,20-23,26-33,35-38H,7H2,1H3;3*1H2/t8-,15+,17-,18+,20+,21-,22+,23+,26+,27-;;;/m0.../s1 |
| InChIKey | NLLBWFFSGHKUSY-JPRRWYCFSA-N |
| SMILES | CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)O)O)O)O)O)O.O.O.O |
| Reference | 1.Chobot, V.,Hadacek, F. and Kubocova, L. Effects of selected dietary secondary metabolites on reactive oxygen species production caused by iron(II) autoxidation. Molecules 19(12), 20023-20033 (2014). |
