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Product Name Euxanthone
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Catalog No.: CN05817
CAS No.: 529-61-3
Molecular Formula: C13H8O4
Molecular Weight: 228.2 g/mol
Purity: >=98%
Type of Compound: Xanthones
Physical Desc.: Powder
Source: The roots of Polygala tenuifolia Willd.
Solvent: Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
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Description Euxanthone, a xanthone derivative, attenuates Aβ1-42-induced oxidative stress and apoptosis by triggering Autophagy. Euxanthone exhibits anti-neoplastic and neuroprotective activities[1][2][3].
In Vitro Euxanthone (10-20 μM; 24 h) 损害 OS 细胞以剂量依赖方式迁移的能力,并显着抑制细胞侵袭。Euxanthone 显着降低与纤连蛋白的粘附[1]。 Euxanthone (10-20 μM; 24 h) 通过 miR-21/PDCD4/c-jun 信号通路调节 COX-2 的表达。Euxanthone 对 COX-2 的抑制介导了其抗转移活性[1]。 Cell Migration Assay [1] Cell Line: Osteosarcoma (OS) cells Concentration: 10 μM, 20 μM Incubation Time: 24 h Result: Inhibited cell migration at 24 hr. Western Blot Analysis[1] Cell Line: Osteosarcoma (OS) cells Concentration: 10 μM, 20 μM Incubation Time: 24 h Result: Repressed both the mRNA and protein level of COX-2 in OS cells in a dose-dependent fashion.
In Vivo 在肺转移模型中,Euxanthone (40-80 mg/kg) 可显着减少肺组织中转移结节的数量[1]。 Euxanthone(30-60 mg/kg;口服;每天一次;持续 7 天)治疗使双侧颈总动脉闭塞的小鼠 Bnip3、Beclin1、Pink1、Parkin、p53、Bax、caspase-3 和 LC3 II/I 正常化。Euxanthone 调节由线粒体断裂介导的线粒体应激诱导的线粒体自噬和细胞凋亡[2]。 Animal Model: Forty male ICR mice (20 g) induced cerebral ischemia and reperfusion[2] Dosage: 30 mg/kg, 60 mg/kg Administration: p.o.;once a day; for 7 days Result: Markedly attenuated BCCAO triggered mitochondrial stress and related breakdown.
Density1.5±0.1 g/cm3
Boiling Point472.6±45.0 °C at 760 mmHg
Flash Point191.1±22.2 °C
Exact Mass228.042252
PSA70.67000
LogP1.92
Vapour Pressure0.0±1.2 mmHg at 25°C