Rutin (hydrate)

• CAT Number: R066644
• CAS Number: 250249-75-3
• Molecular Formula: C27H36O19
• Molecular Weight: 664.566
• Purity: ≥95%
• 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

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.

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).