| Weight | 286.239 g/mol |
|---|---|
| Formula | C15H10O6 |
| Hydrogen Acceptors | 6 |
| Hydrogen Donors | 4 |
| Aromatic Rings | 3 |
| Rotatable Bonds | 1 |
luteolin (491-70-3)
Luteoline · 3',4',5,7-Tetrahydroxy-Flavone · 3',4',5,7-Tetrahydroxyflavone
Score:
#1374 in Biochemistry
,
#3315 in Biology
,
#4135 in Chemistry
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- A plant flavone, luteolin, induces expression of Rhizobium meliloti nodulation genes (Science, 1986)
- Flavonoid (Myricetin, Quercetin, Kaempferol, Luteolin, and Apigenin) Content of Edible Tropical Plants (Journal of Agricultural and Food Chemistry, 2001)
- Distribution and Biological Activities of the Flavonoid Luteolin (Mini-reviews in Medicinal Chemistry, 2009)
- Luteolin, a Flavonoid with Potential for Cancer Prevention and Therapy (Current Cancer Drug Targets, 2008)
- Inhibition of Alpha-glucosidase and Amylase by Luteolin, a Flavonoid (Bioscience, Biotechnology, and Biochemistry, 2000)
- Intestinal absorption of luteolin and luteolin 7-O--glucoside in rats and humans (FEBS Letters, 1998)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - Luteoline
- 3',4',5,7-Tetrahydroxy-Flavone
- 3',4',5,7-Tetrahydroxyflavone
-
SMILESC1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)O
-
InChIKeyIQPNAANSBPBGFQ-UHFFFAOYSA-N
- Pubchem - luteolin
- Wikipedia - luteolin
Luteolin is a flavone, a type of flavonoid, with a yellow crystalline appearance.
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