| Size | Price | Stock |
|---|---|---|
| 1g | $29 | In-stock |
| 5 g | Get quote | |
| 10 g | Get quote | |
| We match the lowest price on market. | ||
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| Cat. No. : | HY-114740 |
| M.Wt: | 272.30 |
| Formula: | C19H12O2 |
| Purity: | >98 % |
| Solubility: | DMSO : 25 mg/mL (ultrasonic;warming;heat to 60°C) |
β-Naphthoflavone is an exogenous aryl hydrocarbon receptor (AHR) ligand. β-Naphthoflavone can activate AHR to participate in various biological processes, including cell growth, differentiation, apoptosis, and metabolism. β-Naphthoflavone has antioxidant activity and can exert its antioxidant function by regulating the activity of antioxidant enzymes. β-Naphthoflavone is also a non-carcinogenic CYP1A inducer and can be used to treat aristolochic acid (AAI) induced renal injury[1][2][3]. In Vitro:β-Naphthoflavone (0.1, 1 and 10 µM; 3 days) increases CYP1A1 mRNA levels in HepG2 cells in a dose-dependent manner and decreases the level of labile zinc in HepG2 cells by approximately 5%, 10% and 17%, respectively[1]. β-Naphthoflavone (0-50 µM; 24 h) attenuats the decreased viability and increases apoptosis of neuronal SH-SY5Y cells induced by H2O2[2]. β-Naphthoflavone (10 µM) significantly increases the activities of CAT and SOD enzymes in neuronal SH-SY5Y cells and inhibites p38MAPK to attenuate H2O2 induced damage[2]. In Vivo:β-Naphthoflavone (80 mg/kg, i.p.; once daily for 3 days) protects mice from AAI-induced renal injury and reduces the accumulation of AAI in the mouse kidneys[3].
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