1. Cell Cycle/DNA Damage Autophagy Anti-infection NF-κB Metabolic Enzyme/Protease Immunology/Inflammation Apoptosis PI3K/Akt/mTOR MAPK/ERK Pathway
  2. Antibiotic Topoisomerase Autophagy Bacterial Reactive Oxygen Species Parasite Apoptosis PI3K Akt Caspase JNK AP-1 NF-κB
  3. Berberine

Berberine  (Synonyms: 黄连素; Natural Yellow 18)

目录号: HY-N0716
产品使用指南 技术支持

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。硫酸盐形式 (HY-N0716B) 可提高生物利用度。

在相同的摩尔浓度下,化合物盐形式与游离形式有相同的生物活性,但盐形式 Berberine sulfate 通常具有更好的水溶性和稳定性。

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Berberine Chemical Structure

Berberine Chemical Structure

CAS No. : 2086-83-1

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Customer Review

Other Forms of Berberine:

MCE 顾客使用本产品发表的 45 篇科研文献

WB
Proliferation Assay
Cell Viability Assay

    Berberine purchased from MCE. Usage Cited in: BMC Pharmacol Toxicol. 2023 May 11;24(1):29.  [Abstract]

    Berberine (BBR; 0.625, 1.25, 2.5, 5, 10 µM; 48 h) inhibits the viability of A431cells in a dose-dependent matter.

    Berberine purchased from MCE. Usage Cited in: BMC Pharmacol Toxicol. 2023 May 11;24(1):29.  [Abstract]

    Berberine (BBR; 2.5, 5, 10 µM; 48 h) inhibits EGFR phosphorylation in a dose-dependent matter in A431cells.

    Berberine purchased from MCE. Usage Cited in: BMC Pharmacol Toxicol. 2023 May 11;24(1):29.  [Abstract]

    Berberine (BBR; 2.5 µM; 10 days) significantly inhibits NCI-H441 colony formation.
    • 生物活性

    • 纯度 & 产品资料

    • 参考文献

    生物活性

    Berberine (Natural Yellow 18) is an alkaloid isolated from the Chinese herbal medicine Huanglian, as an antibiotic. Berberine (Natural Yellow 18) induces reactive oxygen species (ROS) generation and inhibits DNA topoisomerase. Berberine (Natural Yellow 18) has antineoplastic properties. The sulfate form (HY-N0716B) improves bioavailability[1].

    IC50 & Target

    ROS[1]
    DNA topoisomerase[1]

    体外研究
    (In Vitro)

    Berberine suLfate (1.25-160 μM;72 hours) 对四种结直肠癌细胞系 LoVo、HCT116、SW480 和 HT-29 的增殖具有潜在的抑制作用[1]
    Berberine suLfate (1.25-160 μM;24-72 小时) 诱导 LoVo 细胞生长的时间和剂量依赖性抑制[1]
    LoVo 细胞暴露于硫酸 Berberine sulfate (10 -80 μM) 24 小时。通过流式细胞仪对 40 μM 小檗碱处理的 LoVo 细胞进行细胞周期分析显示细胞在 G2/M 期积累[1]
    硫酸 Berberine sulfate (10 -80 μM) 抑制细胞周期蛋白 B1、cdc2和cdc25c蛋白在24 h后的表达,尤其是在80.0 μM剂量下[1]
    Berberine hemisulfate 通过抑制细胞分裂蛋白 (FtsZ) 或通过结合 DNA/RNA 并造成 DNA/RNA 损伤,发挥抗菌活性[3]
    Berberine hemisulfate 通过抑制 TNF-α 及其下游通路 AP-1NF-kB 的激活,发挥抗炎活性[4]
    Berberine hemisulfate 通过抑制活性氧 (ROS) 的产生和 caspase 激活,激活 PI3K/Akt 信号通路和上调血红素加氧酶-1 (HO-1) 表达,发挥神经保护活性[5]
    Berberine hemisulfate 通过调节脂质和抑制胰岛素抵抗来改善代谢疾病[6]

    MCE has not independently confirmed the accuracy of these methods. They are for reference only.

    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 IC50 ranged 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].

    MCE has not independently confirmed the accuracy of these methods. They are for reference only.

    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
    中文名称

    黄连素;小檗碱

    结构分类
    初始来源
    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.

    纯度 & 产品资料
    参考文献
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    • 稀释计算器

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    Help & FAQs
    • Do most proteins show cross-species activity?

      Species cross-reactivity must be investigated individually for each product. Many human cytokines will produce a nice response in mouse cell lines, and many mouse proteins will show activity on human cells. Other proteins may have a lower specific activity when used in the opposite species.

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