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

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

货号: JP2003-25G 品牌: Jinpan 标签: 生化试剂

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)  JP2003-5G      5g 450
Berberine Chloride Hydrate 盐酸小檗碱水合物(盐酸黄连素水合物) JP2003-25G 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DJPO(5mg/ml),水(<4mg/ml,微热助溶)

10)化学结构:Berberine Chloride Hydrate 盐酸小檗碱水合物(盐酸黄连素水合物)

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 (DJPO)

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) JP2001-5MG          5mg 120
Berberine 小檗碱(黄连素) JP2001-20MG 20mg 400
Berberine Chloride 盐酸小檗碱(盐酸黄连素) JP2002-20MG 20mg 220
Berberine Chloride 盐酸小檗碱(盐酸黄连素) JP2002-100MG 100mg 600
Berberine Chloride Hydrate 盐酸小檗碱水合物(盐酸黄连素水合物)   JP2003-5G 5g 450
Berberine Chloride Hydrate 盐酸小檗碱水合物(盐酸黄连素水合物) JP2003-25G 25g 1380
Berberine Hydrogen Sulphate 硫酸小檗碱(硫酸氢黄连素) JP2004-20MG 20mg 300
Berberine Hydrogen Sulphate 硫酸小檗碱(硫酸氢黄连素) JP2004-100MG 100mg 760

 

 

 

 

 

规格信息

品牌:

Jinpan

CAS:

141433-60-5

规格:

25g

货期:

咨询客服

Berberine Chloride 盐酸小檗碱(盐酸黄连素)

Berberine Chloride 盐酸小檗碱(盐酸黄连素)

货号: JP2002-100MG 品牌: Jinpan 标签: 生化试剂

描述

Berberine Chloride 盐酸小檗碱(盐酸黄连素)

产品信息

产品名称 产品编号 规格               价格(元)   
Berberine Chloride 盐酸小檗碱(盐酸黄连素)    JP2002-20MG       20mg 220
Berberine Chloride 盐酸小檗碱(盐酸黄连素) JP2002-100MG 100mg 600

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。

本品是盐酸形式的小檗碱,即盐酸小檗碱(Berberine chloride or Berberine hydrochloride),又称为盐酸黄连素,CAS NO. 633-65-8,以冻干粉形式提供,纯度>98%。

产品特性

1)   CAS NO:633-65-8

2)  化学名: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)   同义名:Berberine hydrochloride 盐酸小孽碱,盐酸小孽碱;盐酸黄连素;黄连素盐酸盐;氯化黄连素;Umbellatine;Natural Yellow 18 自然黄18;

4)   分子式:C20H18NO4Cl

5)   分子量:371.81

6)   含量:>98%

7)   外观:浅黄色至黄色结晶性粉末

8)   溶解性:溶于DJPO(40mg/ml,25℃),甲醇、乙醇(<1mg/ml,25℃),H2O(<1mg/ml,25℃)

9)   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 (DJPO)

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) JP2001-5MG          5mg 120
Berberine 小檗碱(黄连素) JP2001-20MG 20mg 400
Berberine Chloride 盐酸小檗碱(盐酸黄连素) JP2002-20MG 20mg 220
Berberine Chloride 盐酸小檗碱(盐酸黄连素) JP2002-100MG 100mg 600
Berberine Chloride Hydrate 盐酸小檗碱水合物(盐酸黄连素水合物)   JP2003-5G 5g 450
Berberine Chloride Hydrate 盐酸小檗碱水合物(盐酸黄连素水合物) JP2003-25G 25g 1380
Berberine Hydrogen Sulphate 硫酸小檗碱(硫酸氢黄连素) JP2004-20MG 20mg 300
Berberine Hydrogen Sulphate 硫酸小檗碱(硫酸氢黄连素) JP2004-100MG 100mg 760

 

 

 

 

 

规格信息

品牌:

Jinpan

CAS:

633-65-8

规格:

100mg

货期:

咨询客服

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

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

货号: JP2003-5G 品牌: Jinpan 标签: 生化试剂

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)  JP2003-5G      5g 450
Berberine Chloride Hydrate 盐酸小檗碱水合物(盐酸黄连素水合物) JP2003-25G 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DJPO(5mg/ml),水(<4mg/ml,微热助溶)

10)化学结构:Berberine Chloride Hydrate 盐酸小檗碱水合物(盐酸黄连素水合物)

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 (DJPO)

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) JP2001-5MG          5mg 120
Berberine 小檗碱(黄连素) JP2001-20MG 20mg 400
Berberine Chloride 盐酸小檗碱(盐酸黄连素) JP2002-20MG 20mg 220
Berberine Chloride 盐酸小檗碱(盐酸黄连素) JP2002-100MG 100mg 600
Berberine Chloride Hydrate 盐酸小檗碱水合物(盐酸黄连素水合物)   JP2003-5G 5g 450
Berberine Chloride Hydrate 盐酸小檗碱水合物(盐酸黄连素水合物) JP2003-25G 25g 1380
Berberine Hydrogen Sulphate 硫酸小檗碱(硫酸氢黄连素) JP2004-20MG 20mg 300
Berberine Hydrogen Sulphate 硫酸小檗碱(硫酸氢黄连素) JP2004-100MG 100mg 760

 

 

 

 

 

规格信息

品牌:

Jinpan

CAS:

141433-60-5

规格:

5g

货期:

咨询客服

Berberine Chloride 盐酸小檗碱(盐酸黄连素)

Berberine Chloride 盐酸小檗碱(盐酸黄连素)

货号: JP2002-20MG 品牌: Jinpan 标签: 生化试剂

描述

Berberine Chloride 盐酸小檗碱(盐酸黄连素)

产品信息

产品名称 产品编号 规格               价格(元)   
Berberine Chloride 盐酸小檗碱(盐酸黄连素)    JP2002-20MG       20mg 220
Berberine Chloride 盐酸小檗碱(盐酸黄连素) JP2002-100MG 100mg 600

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。

本品是盐酸形式的小檗碱,即盐酸小檗碱(Berberine chloride or Berberine hydrochloride),又称为盐酸黄连素,CAS NO. 633-65-8,以冻干粉形式提供,纯度>98%。

产品特性

1)   CAS NO:633-65-8

2)  化学名: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)   同义名:Berberine hydrochloride 盐酸小孽碱,盐酸小孽碱;盐酸黄连素;黄连素盐酸盐;氯化黄连素;Umbellatine;Natural Yellow 18 自然黄18;

4)   分子式:C20H18NO4Cl

5)   分子量:371.81

6)   含量:>98%

7)   外观:浅黄色至黄色结晶性粉末

8)   溶解性:溶于DJPO(40mg/ml,25℃),甲醇、乙醇(<1mg/ml,25℃),H2O(<1mg/ml,25℃)

9)   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 (DJPO)

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) JP2001-5MG          5mg 120
Berberine 小檗碱(黄连素) JP2001-20MG 20mg 400
Berberine Chloride 盐酸小檗碱(盐酸黄连素) JP2002-20MG 20mg 220
Berberine Chloride 盐酸小檗碱(盐酸黄连素) JP2002-100MG 100mg 600
Berberine Chloride Hydrate 盐酸小檗碱水合物(盐酸黄连素水合物)   JP2003-5G 5g 450
Berberine Chloride Hydrate 盐酸小檗碱水合物(盐酸黄连素水合物) JP2003-25G 25g 1380
Berberine Hydrogen Sulphate 硫酸小檗碱(硫酸氢黄连素) JP2004-20MG 20mg 300
Berberine Hydrogen Sulphate 硫酸小檗碱(硫酸氢黄连素) JP2004-100MG 100mg 760

 

 

 

 

 

规格信息

品牌:

Jinpan

CAS:

633-65-8

规格:

20mg

货期:

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Doxycycline Hyclate 盐酸强力霉素(盐酸多西环素)

Doxycycline Hyclate 盐酸强力霉素(盐酸多西环素)

货号: JP0060-25G 品牌: Jinpan 标签: 生化试剂

描述

Doxycycline Hyclate 盐酸强力霉素

产品标签

Doxycycline Hyclate 盐酸强力霉素;Tetracycline Hydrochloride 盐酸四环素;广谱抑菌抗生素 bacteriostatic antibiotics;MMPs Inhibitor广谱金属基质蛋白酶抑制剂;Tet-on/Tet-off调控系统;CAS:24390-14-5;

产品信息

产品名称

产品编号  CAS NO.   规格 价格(元)

Doxycycline Hyclate 盐酸强力霉素          

JP0060-5G 24390-14-5 5g

150

Doxycycline Hyclate 盐酸强力霉素

JP0060-25G 24390-14-5 25g

450

Doxycycline Hyclate 盐酸强力霉素

JP0060-100G 24390-14-5 100g

880

Doxycycline Hyclate 盐酸强力霉素 JP0060-500G 24390-14-5 500g

2280

 

产品描述

盐酸强力霉素(Doxycycline Hyclate,CAS NO:24390-14-5),一种半合成的四环素类抗生素,主要作用于引起呼吸道感染的细菌包括肺炎支原体(Mycoplasma pneumoniae)和流感嗜血杆菌(Haemophilus influenzae),以及某些对β-内酰胺敏感的耐万古霉素肠球菌(VRE)和耐糖肽抗生素的“超级细菌”的生长。作用机制在其能穿透细胞膜与30S核糖体亚基结合,干扰tRNA/mRNA相互作用,最终抑制蛋白合成。强力霉素还具有抗原虫性和驱虫功能。

盐酸强力霉素是一种广谱的基质金属蛋白酶(MMPs)抑制剂,比如I型胶原酶,用来研究伤口治愈和组织重塑。有文献报道,强力霉素能够抑制胶原合成,抑制增殖和迁移,抑制莱姆病诱发的炎症反应,以及增强和促进平滑肌细胞粘附作用。还可通过阻止纤溶酶原系统起到微血管保护作用。常用来筛选含pcDNA3.1抗性质粒的293细胞系,有效工作浓度为2μg/ml。强力霉素也是Tet-on和Tet-off系统中最好的效应物,分别通过调控rtTA(反义Tet转录活化因子)和rTA(Tet转录活化因子)与TRE(Tet应答元件)的结合,来打开和关闭基因表达。适用于体内外研究。

本品以粉末形式提供,可用于分子生物学,以及细胞培养中以去除微生物污染或抗性筛选。细胞培养中常用的工作浓度范围是0.1-12μg/ml。

产品特性

  1. CAS NO:24390-14-5
  2. 英文同义名:Doxycycline hydrochloride hemiethanolate hemihydrate
  3. 中文同义名:多西环素单盐酸半乙醇半水合物,多西环素盐酸盐半乙醇化物半水合物;盐酸多西环素;盐酸脱氧土霉素;
  4. 分子式:C22H24N2O8∙ HCl ∙ ½(H2O) ∙ ½(C2H6O)
  5. 分子量:512.94
  6. 纯度:>97%
  7. 外观:浅黄色至黄色结晶粉末
  8. 含量:800-920 μg/mg(基于干重)
  9. 溶解性:溶于水(50mg/ml,可能需要微热以保证充分溶解)和甲醇,微溶于乙醇,不溶于氯仿。
  10. 化学结构式:Doxycycline Hyclate 盐酸强力霉素(盐酸多西环素)

保存与运输方法

保存:2-8ºC避光干燥保存,4年有效。

运输:室温运输。

注意事项

1)盐酸强力霉素的溶液建议现配现用,但2-8ºC避光,可稳定保存几天。

2)为了您的安全和健康,请穿实验服并戴一次性手套操作。

 

 

 

 

规格信息

品牌:

Jinpan

CAS:

24390-14-5

规格:

25g

货期:

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