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Broussochalcone A

目录号 : GC70853

Broussochalcone A是黄嘌呤氧化酶的抗氧化剂和抑制剂(IC50=2.21 μM),具有清除自由基的活性。

Broussochalcone A Chemical Structure

Cas No.:99217-68-2

规格 价格 库存 购买数量
1 mg
¥2,070.00
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5 mg
¥5,310.00
现货
10 mg
¥8,550.00
现货

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Sample solution is provided at 25 µL, 10mM.

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产品描述

Broussochalcone A is an antioxidant and an inhibitor of Xanthine Oxidase (IC50=2.21 μM), with free radical scavenging activity. Broussochalcone A inhibits iron-induced lipid peroxidation and nitric oxide synthesis in lipopolysaccharide (LPS) -activated macrophages. Broussochalcone A also induces Apoptosis of human renal carcinoma cells by increasing ROS levels and activating FOXO3 signaling pathways.

Broussochalcone A (0.3, 1, and 3 μM; 10 min, Fe induction for another 30 min) inhibits Fe2+ (200 μM)-induced lipid peroxidation in rat brain homogenate[1].
Broussochalcone A (1-30 μM; 30 min) increases DPPH (100 μM)-scavenging activity dose-dependently[1].
Broussochalcone A (0.1-1 μM) inhibits cytochrome c reduction with an IC50 value of 0.5 μM, mostly due to its superoxide anion-scavenging activity and only partially to its inhibition of xanthine oxidase activity[1].
Broussochalcone A (1-20 μM; 24 h) inhibits nitrite production and iNOS protein expression[1].

References:
[1]. Cheng Z, et al. Broussochalcone A, a potent antioxidant and effective suppressor of inducible nitric oxide synthase in lipopolysaccharide-activated macrophages. Biochem Pharmacol. 2001 Apr 15;61(8):939-46.
[2]. Lee HK, et al. Broussochalcone A Induces Apoptosis in Human Renal Cancer Cells via ROS Level Elevation and Activation of FOXO3 Signaling Pathway. Oxid Med Cell Longev. 2021 Oct 27;2021:2800706.

Chemical Properties

Cas No. 99217-68-2 SDF
分子式 C20H20O5 分子量 340.37
溶解度 DMSO : 100 mg/mL (293.80 mM; Need ultrasonic; Hygroscopic DMSO has a significant impact on the solubility of product, please use newly opened DMSO) 储存条件 -20°C
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1 mg 5 mg 10 mg
1 mM 2.938 mL 14.6899 mL 29.3798 mL
5 mM 0.5876 mL 2.938 mL 5.876 mL
10 mM 0.2938 mL 1.469 mL 2.938 mL
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