| Weight | 610.521 g/mol |
|---|---|
| Formula | C27H30O16 |
| Hydrogen Acceptors | 16 |
| Hydrogen Donors | 10 |
| Aromatic Rings | 3 |
| Rotatable Bonds | 6 |
RUTIN (1340-08-5, 153-18-4)
Rutoside · Quercetin-3-Rutinoside · 3-Rhamnosyl-Glucosyl Quercetin
Score:
#1081 in Biochemistry
,
#2791 in Biology
,
#3497 in Chemistry
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- Chelating and free radical scavenging mechanisms of inhibitory action of rutin and quercetin in lipid peroxidation (Biochemical Pharmacology, 1989)
- Evidence for protective and antioxidant properties of rutin, a natural flavone, against ethanol induced gastric lesions. (Journal of Ethnopharmacology, 2000)
- Quercetin and rutin as inhibitors of azoxymethanol-induced colonic neoplasia (Carcinogenesis, 1991)
- Anti-inflammatory properties of plant flavonoids. Effects of rutin, quercetin and hesperidin on adjuvant arthritis in rat. (Farmaco, 2001)
- Pharmacokinetics of quercetin from quercetin aglycone and rutin in healthy volunteers (European Journal of Clinical Pharmacology, 2000)
- Chlorogenic Acid, Quercetin-3-Rutinoside and Black Tea Phenols Are Extensively Metabolized in Humans (Journal of Nutrition, 2003)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - Rutoside
- Quercetin-3-Rutinoside
- 3-Rhamnosyl-Glucosyl Quercetin
- Quercetin 3 Rutinoside
-
SMILESCC1C(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
-
InChIKeyIKGXIBQEEMLURG-UHFFFAOYSA-N
- Pubchem - RUTIN
- Wikipedia - Troxerutin
Troxerutin is a flavonol, a type of flavonoid. It is more accurately a hydroxyethylrutoside. It can be isolated from Sophora japonica, the Japanese pagoda tree.
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