Berberine Chloride Hydrate 盐酸小檗碱水合物(盐酸黄连素水合物)


描述

Berberine Chloride Hydrate 盐酸小檗碱水合物(盐酸黄连素水合物)

产品信息

产品名称 产品编号 规格            价格(元) 
Berberine Chloride Hydrate 盐酸小檗碱水合物(盐酸黄连素水合物)  MS2003-5G      5g 450
Berberine Chloride Hydrate 盐酸小檗碱水合物(盐酸黄连素水合物) MS2003-25G 25g 1380

产品描述

小檗碱(Berberine)是来源于毛茛科药用植物黄连的一种异喹啉类生物碱,具有非常多样的药理作用,包括1)抗肿瘤效应,包括乳腺癌、白血病、黑素瘤、鳞状细胞癌、胰腺癌、肝癌等;2)一种有效的口服降血糖剂,对脂质代谢起到积极效果;3)一种中药抗抑郁剂,一种阻止神经退行性紊乱的神经保护剂;4)减少非酒精性脂肪性肝病(NAFLD)大鼠的肝脂肪含量,也能防止肝星状细胞(HSCs)增殖,HSCs在肝损伤中纤维化发展很关键;5)体外改善促炎症细胞因子诱导的肠道上皮紧密连接损伤,可能是一种靶向诊治药物能够复原肠道疾病状态中的屏障功能;6)可能是一种广谱的抗微生物制剂;另外,小檗碱在紫外光照下发荧光,组织学研究中通常用于肥大细胞颗粒内的肝素染色。

本品是盐酸水合物形式的小檗碱,即盐酸小檗碱水合物(Berberine chloride hydrate or Berberine hydrochloride hydrate),又称为盐酸黄连素水合物,CAS NO. 141433-60-5,以冻干粉形式提供,纯度>98%。

产品特性

1)   CAS NO:141433-60-5

2)  化学名: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)   同义名:Berberine hydrochloride hydrate 盐酸小檗碱水合物,氯化小檗碱水合物,盐酸黄连素水合物;黄连素盐酸盐水合物;氯化黄连素水合物;Natural Yellow 18 hydrate 自然黄18水合物;

4)   分子式:C20H18ClNO4·xH2O

5)   分子量:371.81 (as Anhydrous)

6)   纯度:>98.0% (HPLC)

7)   含水量:8-12%

8)   外观:浅黄色至黄色结晶性粉末

9)   溶解性:溶于DMSO(5mg/ml),水(<4mg/ml,微热助溶)

10)化学结构:

保存与运输方法

保存:2-8ºC干燥保存,或置于-20℃长期保存,至少2年有效。

运输:常温运输。

产品应用【来自文献,仅做参考】

文献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

体内研究:

实验目的(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.

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

实验方法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.

动物模型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.

实验方法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.

文献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

体外研究:

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

细胞类型(Cell type):MG-63 human osteosarcoma cell line (wild type)

药物配制(Preparation):Berberine was dissolved in dimethyl sulfoxide (DMSO)

实验方法(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.

文献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

体内研究:

实验目的(Purpose):To study the in vivo antitumor effects of berberine

动物模型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.

实验方法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).

给药途径(Administration):Oral gavage

 

注意事项

1)   本品并非商业化药物,不可用作临床或诊断用途,仅限科研使用。

2)   为了您的安全和健康,请穿实验服并戴一次性手套操作。

相关产品

产品名称 产品编号 规格              价格(元)  
Berberine 小檗碱(黄连素) MS2001-5MG          5mg 120
Berberine 小檗碱(黄连素) MS2001-20MG 20mg 400
Berberine Chloride 盐酸小檗碱(盐酸黄连素) MS2002-20MG 20mg 220
Berberine Chloride 盐酸小檗碱(盐酸黄连素) MS2002-100MG 100mg 600
Berberine Chloride Hydrate 盐酸小檗碱水合物(盐酸黄连素水合物)   MS2003-5G 5g 450
Berberine Chloride Hydrate 盐酸小檗碱水合物(盐酸黄连素水合物) MS2003-25G 25g 1380
Berberine Hydrogen Sulphate 硫酸小檗碱(硫酸氢黄连素) MS2004-20MG 20mg 300
Berberine Hydrogen Sulphate 硫酸小檗碱(硫酸氢黄连素) MS2004-100MG 100mg 760

 

 

 

 

141433-60-5 Berberine Chloride Hydrate 盐酸小檗碱水合物(盐酸黄连素水合物)

产品名称 规格             
Berberine Chloride Hydrate 盐酸小檗碱水合物(盐酸黄连素水合物)        5g
Berberine Chloride Hydrate 盐酸小檗碱水合物(盐酸黄连素水合物) 25g

产品描述

小檗碱(Berberine)是来源于毛茛科药用植物黄连的一种异喹啉类生物碱,具有非常多样的药理作用,包括1)抗肿瘤效应,包括乳腺癌、白血病、黑素瘤、鳞状细胞癌、胰腺癌、肝癌等;2)一种有效的口服降血糖剂,对脂质代谢起到积极效果;3)一种中药抗抑郁剂,一种阻止神经退行性紊乱的神经保护剂;4)减少非酒精性脂肪性肝病(NAFLD)大鼠的肝脂肪含量,也能防止肝星状细胞(HSCs)增殖,HSCs在肝损伤中纤维化发展很关键;5)体外改善促炎症细胞因子诱导的肠道上皮紧密连接损伤,可能是一种靶向诊治药物能够复原肠道疾病状态中的屏障功能;6)可能是一种广谱的抗微生物制剂;另外,小檗碱在紫外光照下发荧光,组织学研究中通常用于肥大细胞颗粒内的肝素染色。

本品是盐酸水合物形式的小檗碱,即盐酸小檗碱水合物(Berberine chloride hydrate or Berberine hydrochloride hydrate),又称为盐酸黄连素水合物,CAS NO. 141433-60-5,以冻干粉形式提供,纯度>98%。

产品特性

1)   CAS NO:141433-60-5

2)  化学名: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)   同义名:Berberine hydrochloride hydrate 盐酸小檗碱水合物,氯化小檗碱水合物,盐酸黄连素水合物;黄连素盐酸盐水合物;氯化黄连素水合物;Natural Yellow 18 hydrate 自然黄18水合物;

4)   分子式:C20H18ClNO4·xH2O

5)   分子量:371.81 (as Anhydrous)

6)   纯度:>98.0% (HPLC)

7)   含水量:8-12%

8)   外观:浅黄色至黄色结晶性粉末

9)   溶解性:溶于DMSO(5mg/ml),水(<4mg/ml,微热助溶)

10)化学结构:

保存与运输方法

保存:2-8ºC干燥保存,或置于-20℃长期保存,至少2年有效。

运输:常温运输。

产品应用【来自文献,仅做参考】

文献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

体内研究:

实验目的(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.

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

实验方法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.

动物模型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.

实验方法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.

文献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

体外研究:

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

细胞类型(Cell type):MG-63 human osteosarcoma cell line (wild type)

药物配制(Preparation):Berberine was dissolved in dimethyl sulfoxide (DMSO)

实验方法(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.

文献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

体内研究:

实验目的(Purpose):To study the in vivo antitumor effects of berberine

动物模型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.

实验方法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).

给药途径(Administration):Oral gavage

注意事项

1)   本品并非商业化药物,不可用作临床或诊断用途,仅限科研使用。

2)   为了您的安全和健康,请穿实验服并戴一次性手套操作。

相关产品

规格                
Berberine 小檗碱(黄连素)           5mg
Berberine 小檗碱(黄连素) 20mg
Berberine Chloride 盐酸小檗碱(盐酸黄连素) 20mg
Berberine Chloride 盐酸小檗碱(盐酸黄连素) 100mg
Berberine Chloride Hydrate 盐酸小檗碱水合物(盐酸黄连素水合物)   5g
Berberine Chloride Hydrate 盐酸小檗碱水合物(盐酸黄连素水合物) 25g
Berberine Hydrogen Sulphate 硫酸小檗碱(硫酸氢黄连素) 20mg
Berberine Hydrogen Sulphate 硫酸小檗碱(硫酸氢黄连素) 100mg

 

Arabinofuranosyl-guanine (Ara-G) Hydrate 阿糖鸟苷水合物


描述

Arabinofuranosyl-guanine (Ara-G) Hydrate 阿糖鸟苷水合物

产品信息

产品名称 产品编号 规格 价格(元)
Arabinofuranosyl-guanine (Ara-G) Hydrate 阿糖鸟苷水合物   MS0240-10MG   10mg         980
Arabinofuranosyl-guanine (Ara-G) Hydrate 阿糖鸟苷水合物 MS0240-50MG 50mg 3200

产品描述

阿糖鸟苷水合物(Arabinofuranosyl-guanine Hydrate, Ara-G Hydrate),也称为9-β-D-阿拉伯呋喃糖基鸟嘌呤水合物(9-β-D-Arabinofuranosyl guanine hydrate),能够被细胞激酶转化为有活性的5’-三磷酸形式,Ara-GTP。随后,Ara-GTP插入DNA,抑制DNA合成并诱导凋亡。Ara-G也是一种抗肿瘤和抗代谢药物。

产品特性

1)   CAS NO:38819-10-2 (anhydrous) 

2)   英文同义名:Ara-G Hydrate; 9-β-D-Arabinofuranosyl guanine hydrate; Guanine 9-β-D-Arabinofuranoside Hydrate; Guanine arabinoside;

3)   中文同义名:9-β-D-阿拉伯呋喃糖基鸟嘌呤水合物;鸟嘌呤9-β-D-阿拉伯呋喃糖苷水合物;阿糖鸟苷水合物;

4)   分子式:C10H13N5O5·xH2O

5)   分子量:283.24 (anhydrous basis)

6)   纯度:≥98%

7)   外观:白色至类白色结晶性粉末

8)   溶解性:溶于DMSO(>10 mg/ml),不溶于水

9)   化学结构式:

保存与运输方法

保存:2-8°C保存,2年稳定。

运输:室温运输。

注意事项

1)   本品不是临床药物,只能用于科研用途,不能用于诊断或临床用途。

2)  为了您的安全和健康,请穿实验服并戴一次性手套操作。

Arabinofuranosyl-guanine (Ara-G) Hydrate 阿糖鸟苷水合物


描述

Arabinofuranosyl-guanine (Ara-G) Hydrate 阿糖鸟苷水合物

产品信息

产品名称 产品编号 规格 价格(元)
Arabinofuranosyl-guanine (Ara-G) Hydrate 阿糖鸟苷水合物   MS0240-10MG   10mg         980
Arabinofuranosyl-guanine (Ara-G) Hydrate 阿糖鸟苷水合物 MS0240-50MG 50mg 3200

产品描述

阿糖鸟苷水合物(Arabinofuranosyl-guanine Hydrate, Ara-G Hydrate),也称为9-β-D-阿拉伯呋喃糖基鸟嘌呤水合物(9-β-D-Arabinofuranosyl guanine hydrate),能够被细胞激酶转化为有活性的5’-三磷酸形式,Ara-GTP。随后,Ara-GTP插入DNA,抑制DNA合成并诱导凋亡。Ara-G也是一种抗肿瘤和抗代谢药物。

产品特性

1)   CAS NO:38819-10-2 (anhydrous) 

2)   英文同义名:Ara-G Hydrate; 9-β-D-Arabinofuranosyl guanine hydrate; Guanine 9-β-D-Arabinofuranoside Hydrate; Guanine arabinoside;

3)   中文同义名:9-β-D-阿拉伯呋喃糖基鸟嘌呤水合物;鸟嘌呤9-β-D-阿拉伯呋喃糖苷水合物;阿糖鸟苷水合物;

4)   分子式:C10H13N5O5·xH2O

5)   分子量:283.24 (anhydrous basis)

6)   纯度:≥98%

7)   外观:白色至类白色结晶性粉末

8)   溶解性:溶于DMSO(>10 mg/ml),不溶于水

9)   化学结构式:

保存与运输方法

保存:2-8°C保存,2年稳定。

运输:室温运输。

注意事项

1)   本品不是临床药物,只能用于科研用途,不能用于诊断或临床用途。

2)  为了您的安全和健康,请穿实验服并戴一次性手套操作。