產品簡介:
Berberine
Chloride 鹽酸小檗堿(鹽酸黃連素)
產品信息
產品名稱
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產品編號
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規格
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價格(元)
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Berberine Chloride 鹽酸小檗堿(鹽酸黃連素)
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MS2002-20MG
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20mg
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220
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Berberine Chloride 鹽酸小檗堿(鹽酸黃連素)
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MS2002-100MG
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100mg
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600
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產品描述
小檗堿(Berberine)是來源于毛茛科藥用植物黃連的一種異喹啉類生物堿,具有非常多樣的藥理作用,包括1)抗腫瘤效應,包括乳腺癌、白血病、黑素瘤、鱗狀細胞癌、胰腺癌、肝癌等;2)一種有效的口服降血糖劑,對脂質代謝起到積極效果;3)一種中藥抗抑郁劑,一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?。∟AFLD)大鼠的肝脂肪含量,也能防止肝星狀細胞(HSCs)增殖,HSCs在肝損傷中纖維化發展很關鍵;5)體外改善促炎癥細胞因子誘導的腸道上皮緊密連接損傷,可能是一種靶向診治藥物能夠復原腸道疾病狀態中的屏障功能;6)可能是一種廣譜的抗微生物制劑;另外,小檗堿在紫外光照下發熒光,組織學研究中通常用于肥大細胞顆粒內的肝素染色。
本品是鹽酸形式的小檗堿,即鹽酸小檗堿(Berberine
chloride or Berberine hydrochloride),又稱為鹽酸黃連素,CAS NO. 633-65-8,以凍干粉形式提供,純度>98%。
產品特性
1) CAS NO:633-65-8
2) 化學名:9,10-dimethoxy-5,6-dihydro-[1,3]dioxolo[4,5-g]isoquinolino[3,2-a]isoquinolin-7-ium
chloride; 5,6- Dihydro-9,10-dimethoxybenzo[g]-1,3-benzodioxolo[5,6-a]quinolizinium
Chloride; 7,8,13,13a-Tetradehydro- 9,10-dimethoxy-2,3-(methylenedioxy)berbinium
Chloride;
3) 同義名:Berberine
hydrochloride 鹽酸小孽堿,鹽酸小孽堿;鹽酸黃連素;黃連素鹽酸鹽;氯化黃連素;Umbellatine;Natural
Yellow 18 自然黃18;
4) 分子式:C20H18NO4Cl
5)
分子量:371.81
6)
含量:>98%
7)
外觀:淺黃色至黃色結晶性粉末
8)
溶解性:溶于DMSO(40mg/ml,25℃),甲醇、乙醇(<1mg/ml,25℃),H2O(<1mg/ml,25℃)
9)
化學結構:
保存與運輸方法
保存:2-8oC干燥保存,或置于-20℃長期保存,至少2年有效。
運輸:常溫運輸。
產品應用【來自文獻,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
體內研究:
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.
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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.
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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
體內研究:
實驗目的(Purpose):To study the in vivo antitumor effects of berberine
動物模型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
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注意事項
1)
本品并非商業化藥物,不可用作臨床或診斷用途,僅限科研使用。
2)
為了您的安全和健康,請穿實驗服并戴一次性手套操作。
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— —Written/Edited by V. Shallan【版權歸MKBio懋康所有】
上海懋康生物科技有限公司是一家涉足于生命科學和生物技術領域研究的試劑、儀器和實驗室消耗品與實驗服務工作,主要從事細胞生物學、植物學、分子生物學、免疫學、生物化學、蛋白組學。生物制藥與診斷試劑研發生產等領域。 本公司秉承“以人為本,以誠為信、合同守信”的經營理念。堅持"品質保障"的原則為廣大客戶提供優質產品。
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