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Berberine chloride (鹽酸小檗jian)

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  • 型號

    HY-18258

  • 品牌

    MCE

  • 廠商性質(zhì)

    代理商

  • 所在地

    杭州市

規(guī)格

100mg 660元 10000支可售

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CAS號 633-65-8 產(chǎn)地 國產(chǎn)
規(guī)格 100mg 級別 化工級
證書 ISO系列證書
Berberine chloride 是一種生物堿,常用作抗生su。Berberine chloride 誘導(dǎo)活性氧 (ROS) 生成并抑制 DNA 拓?fù)洚悩?gòu)酶 (topoisomerase)。

Berberine chloride  (Synonyms: 鹽酸小檗jian; Natural Yellow 18 chloride)

Berberine chloride 是一種生物堿,常用作抗生su。Berberine chloride 誘導(dǎo)活性氧 (ROS) 生成并抑制 DNA 拓?fù)洚悩?gòu)酶 (topoisomerase)。

生物活性

Berberine chloride is an alkaloid that acts as an antibiotic. Berberine chloride induces reactive oxygen species (ROS) generation and inhibits DNA topoisomerase. Antineoplastic properties[1].


IC50 & Target

ROS[1]
DNA topoisomerase[1]


體外研究(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].

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).


體內(nèi)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

NCT NumberSponsorConditionStart DatePhase
NCT03609892Xijing Hospital of Digestive Diseases
Gastric Ulcer|Chronic Gastritis|Gastric Cancer|Helicobacter Pylori Infection|Gastritis
August 1, 2018Phase 4
NCT02226185Shanghai Jiao Tong University School of Medicine
Colorectal Adenoma
November 2014Phase 2|Phase 3
NCT03378934Peking Union Medical College Hospital
Coronary Artery Disease|Percutaneous Coronary Intervention
September 26, 2018Phase 4


分子量:371.81


性狀:Solid


Formula:C20H18ClNO4


CAS 號:633-65-8


中文名稱:鹽酸小檗jian;鹽酸黃連su;鹽酸黃蓮素


運(yùn)輸條件:Room temperature in continental US; may vary elsewhere.


儲存方式:

4°C, sealed storage, away from moisture

*In solvent : -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture)


溶解性數(shù)據(jù)


In Vitro: 

DMSO : 12.5 mg/mL (33.62 mM; Need ultrasonic)

H2O : < 0.1 mg/mL (ultrasonic) (insoluble)

配制儲備液
濃度溶劑體積質(zhì)量1 mg5 mg10 mg
1 mM2.6895 mL13.4477 mL26.8955 mL
5 mM0.5379 mL2.6895 mL5.3791 mL
10 mM0.2690 mL1.3448 mL2.6895 mL
*

請根據(jù)產(chǎn)品在不同溶劑中的溶解度選擇合適的溶劑配制儲備液;一旦配成溶液,請分裝保存,避免反復(fù)凍融造成的產(chǎn)品失效。
儲備液的保存方式和期限:-80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture)。-80°C 儲存時,請在 6 個月內(nèi)使用,-20°C 儲存時,請在 1 個月內(nèi)使用。

In Vivo:

以下溶解方案都請先按照 In Vitro 方式配制澄清的儲備液,再依次添加助溶劑:

——為保證實驗結(jié)果的可靠性,澄清的儲備液可以根據(jù)儲存條件,適當(dāng)保存;體內(nèi)實驗的工作液,建議您現(xiàn)用現(xiàn)配,當(dāng)天使用; 以下溶劑前顯示的百
分比是指該溶劑在您配制終溶液中的體積占比;如在配制過程中出現(xiàn)沉淀、析出現(xiàn)象,可以通過加熱和/或超聲的方式助溶

  • 1.


    請依序添加每種溶劑: 0.5% CMC-Na/saline water

    Solubility: 11 mg/mL (29.59 mM); Suspended solution; Need ultrasonic


  • 2.


    請依序添加每種溶劑: PBS

    Solubility: 10 mg/mL (26.90 mM); Suspended solution; Need ultrasonic


  • 3.


    請依序添加每種溶劑: 10% DMSO    40% PEG300    5% Tween-80    45% saline

    Solubility: ≥ 1.25 mg/mL (3.36 mM); Clear solution


  • 4.


    請依序添加每種溶劑: 10% DMSO    90% (20% SBE-β-CD in saline)

    Solubility: ≥ 1.25 mg/mL (3.36 mM); Clear solution


參考文獻(xiàn)

[1]. Cai Y, et al. Berberine inhibits the growth of human colorectal adenocarcinoma in vitro and in vivo. J Nat Med. 2014 Jan;68(1):53-62.  [Content Brief]


注:產(chǎn)品僅用于科研

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