| Weight | 464.379 g/mol |
|---|---|
| Formula | C21H20O12 |
| Hydrogen Acceptors | 12 |
| Hydrogen Donors | 8 |
| Aromatic Rings | 3 |
| Rotatable Bonds | 4 |
Isoquercitrin (482-35-9)
Score:
#802 in Biochemistry
,
#2673 in Chemistry
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- Anti-inflammatory activity of quercetin and isoquercitrin in experimental murine allergic asthma (Inflammation Research, 2007)
- Isoquercitrin is the most effective antioxidant in the plant Thuja orientalis and able to counteract oxidative-induced damage to a transformed cell line (RGC-5 cells). (Neurochemistry International, 2010)
- Isoquercitrin: pharmacology, toxicology, and metabolism. (Food and Chemical Toxicology, 2014)
- Effect of acyl donor chain length on isoquercitrin acylation and biological activities of corresponding esters (Process Biochemistry, 2010)
- Difference in absorption of the two structurally similar flavonoid glycosides, hyperoside and isoquercitrin, in rats. (European Journal of Pharmaceutics and Biopharmaceutics, 2005)
- Enzymatically Modified Isoquercitrin, -Oligoglucosyl Quercetin 3-O-Glucoside, Is Absorbed More Easily than Other Quercetin Glycosides or Aglycone after Oral Administration in Rats (Biological & Pharmaceutical Bulletin, 2009)
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SMILESC1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O
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InChIKeyOVSQVDMCBVZWGM-UHFFFAOYSA-N
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