Luteolin | 491-70-3
$26.00 - $157.00
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Cat. No.: LTOL-0.2 (for 10mM×0.2ml)
Cat. No.: LTOL-25 (for 25mg)
Cat. No.: LTOL-100 (for 100mg)
Description
Luteolin (also known as Luteoline), a flavonoid compound, is a potent inhibitor of Nrf2. It possesses anti-inflammatory and anti-cancer properties, inducing apoptosis and cell cycle arrest, and inhibiting metastasis and angiogenesis in various cancer cell lines, including human non-small lung cancer cells.
Basic Information
- Aliases: Luteoline; Digitoflavone; Daphneflavonol; Flavopurpol; Luteolol
- Source: Siphonostegia chinensis Benth.; Lonicera japonica Thunb.
- Compound type: Flavonoids > Flavones
- Chemical Formula: C15H10O6
- Molecular Weight: 286.24
- CAS Number: 491-70-3
- Purity: 98%, HPLC
- Solvent/Solubility: DMSO: ≥ 100 mg/mL (349.36 mM)
- Solution Preparation: 5mg can be dissolved in 1.75ml of DMSO, or alternatively, 2.86mg can be dissolved in 1ml of DMSO, to prepare a 10mM solution.
Signaling Pathway
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In Vitro Study
Luteolin treatment (0-160 µM; 24 hours; NCI-H460 cells) inhibits the viability of NCI-H460 cells in a concentration-dependent manner. Treatment with Luteolin (20-80 µM; 24 hours; NCI-H460 cells) leads to an accumulation of cells in the S phase. Moreover, treatment with Luteolin (320-580 µM; 48 hours; NCI-H460 cells) induces apoptosis. Additionally, Luteolin treatment (20-80 µM; 24 hours; NCI-H460 cells) increases the protein expression levels of apoptotic regulatory proteins, such as the Bax/Bcl-2 ratio, in a concentration-dependent manner. However, only 80 µM Luteolin inhibits the expression of Bad. Furthermore, Luteolin decreases the expression of Sirt1 in the NCI-H460 cell line in a concentration-dependent manner.
In Vivo Study
Luteolin (10-100 mg/kg; oral gavage; daily; for 12 weeks; adult male Wistar rats) exhibits antioxidant properties and can effectively protect against non-alcoholic steatohepatitis by targeting the pro-inflammatory IL-1 and Il-18 pathways in rats fed with a high carbohydrate/high fat diet.
Clinical Trial
NCT03288298: Tongue Neoplasms|Carcinoma, Early Phase 1.
Storage
Store at -20°C for at least one year. The solid powder is stable at 4°C for at least one month. If dissolved in a non-DMSO solvent, it is recommended to aliquot and store at -80°C for up to six months.
Precautions
- This product may have a certain degree of toxicity to the human body. Please take appropriate precautions to avoid direct contact with the body or inhalation.
- This product is for scientific research use only by professionals and is not intended for clinical diagnosis or treatment, food, or pharmaceutical purposes. It should not be stored in ordinary residential areas.
- For your safety and health, please wear laboratory attire and disposable gloves while handling.
Only for research and not intended for treatment of humans or animals
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