| Weight | 448.38 g/mol |
|---|---|
| Formula | C21H20O11 |
| Hydrogen Acceptors | 11 |
| Hydrogen Donors | 7 |
| Aromatic Rings | 3 |
| Rotatable Bonds | 3 |
quercitrin (522-12-3)
quercetrin · quercetin-3-L-rhamnoside · quercetin 3-O-rhamnoside
Score:
#1497 in Biochemistry
,
#3507 in Biology
,
#4390 in Chemistry
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- In vivo quercitrin anti-inflammatory effect involves release of quercetin, which inhibits inflammation through down-regulation of the NF-B pathway (European Journal of Immunology, 2005)
- Tartary Buckwheat (Fagopyrum tataricum Gaertn.) as a Source of Dietary Rutin and Quercitrin (Journal of Agricultural and Food Chemistry, 2003)
- Quercetin, but not rutin and quercitrin, prevention of H2O2-induced apoptosis via anti-oxidant activity and heme oxygenase 1 gene expression in macrophages. (Biochemical Pharmacology, 2005)
- The intestinal antiinflammatory effect of quercitrin is associated with an inhibition in iNOS expression (British Journal of Pharmacology, 2004)
- Effect of quercitrin on acute and chronic experimental colitis in the rat. (Journal of Pharmacology and Experimental Therapeutics, 1996)
- Effect of quercitrin on the early stages of hapten induced colonic inflammation in the rat. (Life Sciences, 2002)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - quercetrin
- quercetin-3-L-rhamnoside
- quercetin 3-O-rhamnoside
-
SMILESCC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O
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InChIKeyOXGUCUVFOIWWQJ-UHFFFAOYSA-N
- Pubchem - quercitrin
- Wikipedia - quercitrin
Quercitrin is a glycoside formed from the flavonoid quercetin and the deoxy sugar rhamnose. Austrian chemist Heinrich Hlasiwetz (1825-1875) is remembered for his chemical analysis of quercitrin.
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quercitrin
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