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Berberine Chloride Hydrate 鹽酸小(xiǎo)檗堿水(shuǐ)合物(wù)(鹽酸黃連素水(shuǐ)合物(wù))
目錄号 MS2003-25G 售價 1380.00元
規格 25g 運輸溫度 室溫運輸
其他名稱 Berberine hydrochloride hydrate 鹽酸小(xiǎo)檗堿水(shuǐ)合物(wù),氯化小(xiǎo)檗堿水(shuǐ)合物(wù),鹽酸黃連素水(shuǐ)合物(wù); 保存溫度 2-8℃保存
CAS号 141433-60-5 有效期 2年(nián)
應用 抗腫瘤化合物(wù) 訂購數量
産品簡介:

Berberine Chloride Hydrate 鹽酸小(xiǎo)檗堿水(shuǐ)合物(wù)(鹽酸黃連素水(shuǐ)合物(wù))


産品信息

産品名稱

産品編号

規格           

價格(元) 

Berberine Chloride Hydrate 鹽酸小(xiǎo)檗堿水(shuǐ)合物(wù)(鹽酸黃連素水(shuǐ)合物(wù)) 

MS2003-5G     

5g

450

Berberine Chloride Hydrate 鹽酸小(xiǎo)檗堿水(shuǐ)合物(wù)(鹽酸黃連素水(shuǐ)合物(wù))

MS2003-25G

25g

1380


産品描述

小(xiǎo)檗堿(Berberine)是來源于毛茛科藥用植物(wù)黃連的一(yī)種異喹啉類生(shēng)物(wù)堿,具有非常多(duō)樣的藥理作用,包括1)抗腫瘤效應,包括乳腺癌、白(bái)血病、黑(hēi)素瘤、鱗狀細胞癌、胰腺癌、肝癌等;2)一(yī)種有效的口服降血糖劑,對脂質代謝起到(dào)積極效果;3)一(yī)種中藥抗抑郁劑,一(yī)種阻止神經退行性紊亂的神經保護劑;4)減少非酒精性脂肪性肝病(NAFLD)大鼠的肝脂肪含量,也能(néng)防止肝星狀細胞(HSCs)增殖,HSCs在肝損傷中纖維化發展很關鍵;5)體外改善促炎症細胞因子誘導的腸道上(shàng)皮緊密連接損傷,可能(néng)是一(yī)種靶向診治藥物(wù)能(néng)夠複原腸道疾病狀态中的屏障功能(néng);6)可能(néng)是一(yī)種廣譜的抗微生(shēng)物(wù)制劑;另外,小(xiǎo)檗堿在紫外光(guāng)照(zhào)下(xià)發熒光(guāng),組織學研究中通(tōng)常用于肥大細胞顆粒内的肝素染色。

本品是鹽酸水(shuǐ)合物(wù)形式的小(xiǎo)檗堿,即鹽酸小(xiǎo)檗堿水(shuǐ)合物(wù)(Berberine chloride hydrate or Berberine hydrochloride hydrate),又(yòu)稱為(wèi)鹽酸黃連素水(shuǐ)合物(wù),CAS NO. 141433-60-5,以凍幹粉形式提供,純度>98%。


産品特性

1)   CAS NO:141433-60-5

2)  化學名:9,10-dimethoxy-5,6-dihydro-[1,3]dioxolo[4,5-g]isoquinolino[3,2-a]isoquinolin-7-ium chloride hydrate; 5,6- Dihydro-9,10-dimethoxybenzo[g]-1,3-benzodioxolo[5,6-a]quinolizinium Chloride hydrate;

3)   同義名:Berberine hydrochloride hydrate 鹽酸小(xiǎo)檗堿水(shuǐ)合物(wù),氯化小(xiǎo)檗堿水(shuǐ)合物(wù),鹽酸黃連素水(shuǐ)合物(wù);黃連素鹽酸鹽水(shuǐ)合物(wù);氯化黃連素水(shuǐ)合物(wù);Natural Yellow 18 hydrate 自(zì)然黃18水(shuǐ)合物(wù);

4)   分子式:C20H18ClNO4·xH2O

5)   分子量:371.81 (as Anhydrous)

6)   純度:>98.0% (HPLC)

7)   含水(shuǐ)量:8-12%

8)   外觀:淺黃色至黃色結晶性粉末

9)   溶解性:溶于DMSO(5mg/ml),水(shuǐ)(<4mg/ml,微熱助溶)

10)化學結構:


保存與運輸方法

保存:2-8ºC幹燥保存,或置于-20℃長(cháng)期保存,至少2年(nián)有效。

運輸:常溫運輸。



産品應用【來自(zì)文獻,僅做參考】

文獻1,Lee YS et al.Berberine, a natural plant product, activates AMP-activated protein kinase with beneficial metabolic effects in diabetic and insulin-resistant states.Diabetes. 2006 Aug;55(8):2256-64. PMID: 16873688

體内研究:

實驗目的(Purpose): Berberine has antidiabetic properties, although its mode of action is unknown. Here, we have investigated the metabolic effects of Berberine in two animal models of insulin resistance and in insulin- responsive cell lines.

動物(wù)模型I(Animal Model I):Obese and diabetic C57BLKS/J-Leprdb/Leprdbmale mice

實驗方法I(Assay I):From 12 weeks of age, berberine was injected intraperitoneally (5 mg · kg body wt−1·

day−1) into the mice for 26 days.

動物(wù)模型II(Animal Model II):Wistar rats (250 g)were acclimatized in communal cages at 22°C, with a 12-h light 12-h dark cycle (lights on at 0600) for 1 week and had access to a standard chow diet and water ad libitum. Rats were then randomly assigned to receive either the standard chow diet as the control group (CH group) or a high-fat (60% calories as saturated fat) diet for 4 weeks.

實驗方法II(Assay II):After 2 weeks of feeding, rats were randomly assigned to receive oral administration of either vehicle (0.5% methylcellulose) or berberine (380 mg · kg−1· day−1) by gavage for the last 2 weeks.

文獻2,Zhu Y et al. Berberine induces apoptosis and DNA damage in MG-63 human osteosarcoma cells.Mol Med Rep. 2014 Oct;10(4):1734-8. PMID: 25050485

體外研究:

實驗目的(Purpose):To investigate the cytotoxic effect of berberine on MG-63 cells

細胞類型(Cell type):MG-63 human osteosarcoma cell line (wild type)

藥物(wù)配制(Preparation):Berberine was dissolved in dimethyl sulfoxide (DMSO)

實驗方法(Assay):MG-63 cells were seeded at a density of 1×104cells/well in 100 μl of cell culture medium and then placed in a 96-well plate. Following 12 h of incubation, the cells were treated with 0, 20, 40, 80 μM berberine for 12 and 24 h. MTT was used to detect cell cytotoxicity.

文獻3,Chu SC et al.Berberine reverses epithelial-to-mesenchymal transition and inhibits metastasis and tumor-induced angiogenesis in human cervical cancer cells. Mol Pharmacol. 2014 Dec;86(6):609-23. PMID: 25217495

體内研究:

實驗目的(Purpose):To study the in vivo antitumor effects of berberine

動物(wù)模型I(Animal Model I):After subcutaneous implantation of SiHa cells, BALB/c nude mice (n = 5 for each group) were treated with placebo or berberine and then analyzed for tumor growth.

實驗方法I(Assay I):The mice were randomly divided into three groups (n = 5 for each group) and fed by oral gavage with placebo (control) and berberine (10 and 20 mg/kg per day).

給藥途徑(Administration):Oral gavage

 

注意事(shì)項

1)   本品并非商業(yè)化藥物(wù),不可用作臨床或診斷用途,僅限科研使用。

2)   為(wèi)了您的安全和健康,請穿實驗服并戴一(yī)次性手套操作。


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 — —Written/Edited by V. Shallan【版權歸MKBio懋康所有】

 

 

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