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Product Packaging | 0.5-5kg/ bag |
Synonyms | 2-(3, 4-dihydroxyphenyl)-5, 7-dihydroxy-4h-1-benzopyran-4-on; 3', 4', 5, 7-TETRAHYDROXYFLAVONE, FLACITRAN, LUTEOLOL |
EINECS | 207-741-0 |
Content Specification | 0.98 |
Molecular Formula | C15H10O6 |
Formula Weight | 286.24 |
Melting Point | ~330°C(lit.) |
Boiling Point | 348.61°C (rough estimate) |
Density | 1.2981 g/cm3(rough estimate) |
Form | Powder |
Color | Yellow |
Solubility | Methanol (Slightly, Heated) |
Water Solubility | Soluble in aqueous alkaline solutions (1.4 mg/ml), ethanol (~5 mg/ml), dimethyl sulfoxide (7 mg/ml), 1eq. Sodium hydroxide (5 mM), dimethylformamide (~20 mg/ml), water (1 mg/ml) at 25°C and methanol. |
Vapor Pressure | 1.4413 (estimate) |
pKa | 6.50±0.40(Predicted) |
BRN | 292084 |
InChIKey | IQPNAANSBPBGFQ-UHFFFAOYSA-N |
LogP | 2.4 |
Hazard Codes | Xi |
Risk Statements | 36/37/38 |
Safety Statements | 26-36-36/37/39 |
WGK Germany | 3 |
RTECS | LK9275210 |
HS Code | 29329990 |
Definition | ChEBI: Luteolin is a tetrahydroxyflavone in which the four hydroxy groups are located at positions 3', 4', 5 and 7. It is thought to play an important role in the human body as an antioxidant, a free radical scavenger, an anti-inflammatory agent and an immune system modulator as well as being active against several cancers. |
Biochem/physiol Actions | Hydroxylated flavone derivative, a strong antioxidant and radical scavenger. Suggested to play a role in prevention of cancer, possibly via the inhibition of fatty acid synthase activity. |
Anticancer Research | It is a flavone with yellow crystalline appearance. Dietary sources of luteolin includeoregano, celery, orange, broccoli, rosemary, green pepper, peppermint, parsley, olive oil, thyme, carrot, dandelion, chamomile tea, and perilla. |
Storage | 2-8°C |
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