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Berberine
本产品不向个人销售,仅用作科学研究,不用于任何人体实验及非科研性质的动物实验。
Berberine图片
CAS NO:2086-83-1

黄连素
Natural Yellow 18
Berberine (Natural Yellow 18) 是从中草药黄连中分离出来的一种生物碱,常用作抗生素。Berberine (Natural Yellow 18) 诱导活性氧 (ROS) 生成并抑制 DNA 拓扑异构酶 (topoisomerase)。Berberine (Natural Yellow 18) 具有抗肿瘤特性。
生物活性

Berberine (Natural Yellow 18) is an alkaloid isolated from the Chinese herbal medicine Huanglian, as anantibiotic. Berberine (Natural Yellow 18) inducesreactive oxygen species(ROS) generation and inhibitsDNAtopoisomerase. Berberine (Natural Yellow 18) has antineoplastic properties[1].

IC50& Target

ROS[1]
DNA topoisomerase[1]

体外研究
(In Vitro)

Berberine (1.25-160 μM; 72 hours) has potential inhibitory effects on the proliferation of four colorectal carcinoma cell lines LoVo, HCT116, SW480, and HT-29[1].
Berberine (1.25-160 μM; 24-72 hours) induces a time- and dose-dependent inhibition of LoVo cell growth[1].
LoVo cells are exposure to Berberine (10-80 μM) for 24 h. Cell cycle analysis of 40 μM Berberine-treated LoVo cells by flow cytometry shows accumulation of cells in the G2/M phase[1].
Berberine (10-80 μM) suppresses cyclin B1, cdc2 and cdc25c protein expression after 24 h, especially at the dose of 80.0 μM[1].

Cell Proliferation Assay[1]

Cell Line:Four colorectal carcinoma cell lines LoVo, HCT116, SW480, and HT-29
Concentration:1.25, 2.5, 5, 10, 20, 40, 80, and 160 μM
Incubation Time:72 hours
Result:Inhibited the proliferation of four cell lines. The IC50ranged from 40.8±4.1 μM (LoVo) to 98.6±2.9 μM (HCT116).

Cell Proliferation Assay[1]

Cell Line:Colorectal carcinoma cell lines LoVo
Concentration:1.25, 2.5, 5, 10, 20, 40, 80, and 160 μM
Incubation Time:24, 48, 72 hours
Result:Induced a time- and dose-dependent inhibition of cell growth. By 72 h, 160.0 μM induced 71.1±1.9 % growth inhibitions in LoVo cells.

Cell Cycle Analysis[1]

Cell Line:LoVo cells
Concentration:0, 10, 20, 40, or 80 μM
Incubation Time:24 hours
Result:Exposure to 40.0 μM induced G2/M-phase cell cycle arrest, an increase in the G2/M-phase population and a progressive decline in the G1 population.

Western Blot Analysis[1]

Cell Line:LoVo cells
Concentration:10, 20, 40, or 80 μM
Incubation Time:24 hours
Result:Suppressed cyclin B1, cdc2 and cdc25c protein expression.
体内研究
(In Vivo)

Berberine (10, 30, or 50 mg/kg/day; gastrointestinal gavage; for 10 consecutive days) inhibits the growth of human colorectal adenocarcinoma in vivo. Berberine at doses of 30 and 50 mg/kg/day taken by gastrointestinal gavage shows inhibitory rates of 33.1% and 45.3% on the human colorectal adenocarcinoma xenograft growth in nude mice[1].

Animal Model:5-week-old BALB/c nu/nu mice with human colorectal adenocarcinoma LoVo xenografts[1]
Dosage:10, 30, or 50 mg/kg/day
Administration:Gastrointestinal gavage; for 10 consecutive days
Result:Showed inhibitory rates of 33.1 % and 45.3 % at doses of 30 and 50 mg/kg/day.
Clinical Trial
分子量

336.36

Formula

C20H18NO4+

CAS 号

2086-83-1

中文名称

黄连素;小檗碱

结构分类
  • Alkaloids
  • Isoquinoline Alkaloids
来源
  • Plants
  • Ranunculaceae
  • Coptis chinensisFranch.
运输条件

Room temperature in continental US; may vary elsewhere.

储存方式

Please store the product under the recommended conditions in the Certificate of Analysis.

 
 
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