HL271(Synonyms: IM156 hydrochloride; HL156A hydrochloride)

上海金畔生物科技有限公司为生命科学和医药研发人员提供生物活性分子抑制剂、激动剂、特异性抑制剂、化合物库、重组蛋白,专注于信号通路和疾病研究领域。

HL271 (Synonyms: IM156 hydrochloride; HL156A hydrochloride)

HL271 (IM156 hydrochloride) 是二甲双胍 (HY-B0627) 的化学衍生物,是一种强效的 AMPK 激活剂,能增加 AMPK 的磷酸化水平。HL271 在动物模型中可缓解与年龄相关的认知障碍。HL271 是一种有效的氧化磷酸化 (OXPHOS) 抑制剂,可用于实体肿瘤的研究。

HL271(Synonyms: IM156 hydrochloride; HL156A hydrochloride)

HL271 Chemical Structure

CAS No. : 1422365-52-3

规格 是否有货
100 mg   询价  
250 mg   询价  
500 mg   询价  

* Please select Quantity before adding items.

HL271 的其他形式现货产品:

IM156

生物活性

HL271 (IM156 hydrochloride; HL156A hydrochloride), a chemical derivative of Metformin (HY-B0627), is a potent AMPK activator that increases AMPK phosphorylation. HL271 attenuates aging-associated cognitive impairment in animal model[1][2]. HL271 is a potent oxidative phosphorylation (OXPHOS) inhibitor which can be used for the research of solid tumors[3].

IC50 & Target

AMPK[1][2], OXPHOS[3]

体外研究
(In Vitro)

HL271 (0.31-10 μM) phosphorylates AMPKα1 Thr172 in a dose- and time-dependent manner in NIH3T3 mouse fibroblast cells[1].
HL271 does not affect the expression of key factors involved in glucose homeostasis such as glucose-6-phosphatase (G6pase) or phosphoenolpyruvate carboxykinase 1 (Pck1)[1].

Shanghai Jinpan Biotech Co Ltd has not independently confirmed the accuracy of these methods. They are for reference only.

Western Blot Analysis[1]

Cell Line: NIH3T3 cells
Concentration: 0.31 μM, 0.62 μM, 1.25 μM, 2.5 μM, 5 μM, 10 μM
Incubation Time: 4 hours
Result: Significantly increased the AMPK phosphorylation rate.

体内研究
(In Vivo)

HL271 does not affect metabolic regulation assessed by body weight, blood glucose, insulin levels and lipid metabolite content in mice with diet-induced obesity[1].
HL271 (50 mg/kg; for 2 months) does not affect body weight, general locomotion, or anxiety[2].
HL271 significantly attenuates the aging-induced decline in novel object recognition memory and spatial working memory[2].
HL271 significantly increases AMPK activation in the hippocampus of aged mice[2].

Shanghai Jinpan Biotech Co Ltd has not independently confirmed the accuracy of these methods. They are for reference only.

Animal Model: C57BL/6J mice (young group/12-16 weeks, old groups/20-22 months)[2]
Dosage: 50 mg/kg
Administration: Oral administration (in drinking water), for 2 months
Result: Attenuated age-related cognitive decline.

Clinical Trial

分子量

351.76

Formula

C13H17ClF3N5O

CAS 号

1422365-52-3

运输条件

Room temperature in continental US; may vary elsewhere.

储存方式

Please store the product under the recommended conditions in the Certificate of Analysis.

参考文献
  • [1]. Row H, et al. HL271, a novel chemical compound derived from metformin, differs from metformin in its effects on the circadian clock and metabolism. Biochem Biophys Res Commun. 2016 Jan 15;469(3):783-9.

    [2]. Bang E, et al. The Improving Effect of HL271, a Chemical Derivative of Metformin, a Popular Drug for Type II Diabetes Mellitus, on Aging-induced Cognitive Decline. Exp Neurobiol. 2018 Feb;27(1):45-56.

    [3]. Sun Young Rha, et al. Phase I study of IM156, a novel potent biguanide oxidative phosphorylation (OXPHOS) inhibitor, in patients with advanced solid tumors. Journal of Clinical Oncology 38(15_suppl):3590-3590.

所有产品仅用作科学研究或药证申报,我们不为任何个人用途提供产品和服务

HL271(Synonyms: IM156 hydrochloride; HL156A hydrochloride)

上海金畔生物科技有限公司为生命科学和医药研发人员提供生物活性分子抑制剂、激动剂、特异性抑制剂、化合物库、重组蛋白,专注于信号通路和疾病研究领域。

HL271 (Synonyms: IM156 hydrochloride; HL156A hydrochloride)

HL271 (IM156 hydrochloride) 是二甲双胍 (HY-B0627) 的化学衍生物,是一种强效的 AMPK 激活剂,能增加 AMPK 的磷酸化水平。HL271 在动物模型中可缓解与年龄相关的认知障碍。HL271 是一种有效的氧化磷酸化 (OXPHOS) 抑制剂,可用于实体肿瘤的研究。

HL271(Synonyms: IM156 hydrochloride; HL156A hydrochloride)

HL271 Chemical Structure

CAS No. : 1422365-52-3

规格 是否有货
100 mg   询价  
250 mg   询价  
500 mg   询价  

* Please select Quantity before adding items.

HL271 的其他形式现货产品:

IM156

生物活性

HL271 (IM156 hydrochloride; HL156A hydrochloride), a chemical derivative of Metformin (HY-B0627), is a potent AMPK activator that increases AMPK phosphorylation. HL271 attenuates aging-associated cognitive impairment in animal model[1][2]. HL271 is a potent oxidative phosphorylation (OXPHOS) inhibitor which can be used for the research of solid tumors[3].

IC50 & Target

AMPK[1][2], OXPHOS[3]

体外研究
(In Vitro)

HL271 (0.31-10 μM) phosphorylates AMPKα1 Thr172 in a dose- and time-dependent manner in NIH3T3 mouse fibroblast cells[1].
HL271 does not affect the expression of key factors involved in glucose homeostasis such as glucose-6-phosphatase (G6pase) or phosphoenolpyruvate carboxykinase 1 (Pck1)[1].

上海金畔生物科技有限公司 has not independently confirmed the accuracy of these methods. They are for reference only.

Western Blot Analysis[1]

Cell Line: NIH3T3 cells
Concentration: 0.31 μM, 0.62 μM, 1.25 μM, 2.5 μM, 5 μM, 10 μM
Incubation Time: 4 hours
Result: Significantly increased the AMPK phosphorylation rate.

体内研究
(In Vivo)

HL271 does not affect metabolic regulation assessed by body weight, blood glucose, insulin levels and lipid metabolite content in mice with diet-induced obesity[1].
HL271 (50 mg/kg; for 2 months) does not affect body weight, general locomotion, or anxiety[2].
HL271 significantly attenuates the aging-induced decline in novel object recognition memory and spatial working memory[2].
HL271 significantly increases AMPK activation in the hippocampus of aged mice[2].

上海金畔生物科技有限公司 has not independently confirmed the accuracy of these methods. They are for reference only.

Animal Model: C57BL/6J mice (young group/12-16 weeks, old groups/20-22 months)[2]
Dosage: 50 mg/kg
Administration: Oral administration (in drinking water), for 2 months
Result: Attenuated age-related cognitive decline.

Clinical Trial

分子量

351.76

Formula

C13H17ClF3N5O

CAS 号

1422365-52-3

运输条件

Room temperature in continental US; may vary elsewhere.

储存方式

Please store the product under the recommended conditions in the Certificate of Analysis.

参考文献
  • [1]. Row H, et al. HL271, a novel chemical compound derived from metformin, differs from metformin in its effects on the circadian clock and metabolism. Biochem Biophys Res Commun. 2016 Jan 15;469(3):783-9.

    [2]. Bang E, et al. The Improving Effect of HL271, a Chemical Derivative of Metformin, a Popular Drug for Type II Diabetes Mellitus, on Aging-induced Cognitive Decline. Exp Neurobiol. 2018 Feb;27(1):45-56.

    [3]. Sun Young Rha, et al. Phase I study of IM156, a novel potent biguanide oxidative phosphorylation (OXPHOS) inhibitor, in patients with advanced solid tumors. Journal of Clinical Oncology 38(15_suppl):3590-3590.

所有产品仅用作科学研究或药证申报,我们不为任何个人用途提供产品和服务

HL271(Synonyms: IM156 hydrochloride; HL156A hydrochloride)

上海金畔生物科技有限公司为生命科学和医药研发人员提供生物活性分子抑制剂、激动剂、特异性抑制剂、化合物库、重组蛋白,专注于信号通路和疾病研究领域。

HL271 (Synonyms: IM156 hydrochloride; HL156A hydrochloride)

HL271 (IM156 hydrochloride) 是二甲双胍 (HY-B0627) 的化学衍生物,是一种强效的 AMPK 激活剂,能增加 AMPK 的磷酸化水平。HL271 在动物模型中可缓解与年龄相关的认知障碍。HL271 是一种有效的氧化磷酸化 (OXPHOS) 抑制剂,可用于实体肿瘤的研究。

HL271(Synonyms: IM156 hydrochloride; HL156A hydrochloride)

HL271 Chemical Structure

CAS No. : 1422365-52-3

规格 是否有货
100 mg   询价  
250 mg   询价  
500 mg   询价  

* Please select Quantity before adding items.

HL271 的其他形式现货产品:

IM156

生物活性

HL271 (IM156 hydrochloride; HL156A hydrochloride), a chemical derivative of Metformin (HY-B0627), is a potent AMPK activator that increases AMPK phosphorylation. HL271 attenuates aging-associated cognitive impairment in animal model[1][2]. HL271 is a potent oxidative phosphorylation (OXPHOS) inhibitor which can be used for the research of solid tumors[3].

IC50 & Target

AMPK[1][2], OXPHOS[3]

体外研究
(In Vitro)

HL271 (0.31-10 μM) phosphorylates AMPKα1 Thr172 in a dose- and time-dependent manner in NIH3T3 mouse fibroblast cells[1].
HL271 does not affect the expression of key factors involved in glucose homeostasis such as glucose-6-phosphatase (G6pase) or phosphoenolpyruvate carboxykinase 1 (Pck1)[1].

Shanghai Jinpan Biotech Co Ltd has not independently confirmed the accuracy of these methods. They are for reference only.

Western Blot Analysis[1]

Cell Line: NIH3T3 cells
Concentration: 0.31 μM, 0.62 μM, 1.25 μM, 2.5 μM, 5 μM, 10 μM
Incubation Time: 4 hours
Result: Significantly increased the AMPK phosphorylation rate.

体内研究
(In Vivo)

HL271 does not affect metabolic regulation assessed by body weight, blood glucose, insulin levels and lipid metabolite content in mice with diet-induced obesity[1].
HL271 (50 mg/kg; for 2 months) does not affect body weight, general locomotion, or anxiety[2].
HL271 significantly attenuates the aging-induced decline in novel object recognition memory and spatial working memory[2].
HL271 significantly increases AMPK activation in the hippocampus of aged mice[2].

Shanghai Jinpan Biotech Co Ltd has not independently confirmed the accuracy of these methods. They are for reference only.

Animal Model: C57BL/6J mice (young group/12-16 weeks, old groups/20-22 months)[2]
Dosage: 50 mg/kg
Administration: Oral administration (in drinking water), for 2 months
Result: Attenuated age-related cognitive decline.

Clinical Trial

分子量

351.76

Formula

C13H17ClF3N5O

CAS 号

1422365-52-3

运输条件

Room temperature in continental US; may vary elsewhere.

储存方式

Please store the product under the recommended conditions in the Certificate of Analysis.

参考文献
  • [1]. Row H, et al. HL271, a novel chemical compound derived from metformin, differs from metformin in its effects on the circadian clock and metabolism. Biochem Biophys Res Commun. 2016 Jan 15;469(3):783-9.

    [2]. Bang E, et al. The Improving Effect of HL271, a Chemical Derivative of Metformin, a Popular Drug for Type II Diabetes Mellitus, on Aging-induced Cognitive Decline. Exp Neurobiol. 2018 Feb;27(1):45-56.

    [3]. Sun Young Rha, et al. Phase I study of IM156, a novel potent biguanide oxidative phosphorylation (OXPHOS) inhibitor, in patients with advanced solid tumors. Journal of Clinical Oncology 38(15_suppl):3590-3590.

所有产品仅用作科学研究或药证申报,我们不为任何个人用途提供产品和服务

Tubulysin IM-3

上海金畔生物科技有限公司为生命科学和医药研发人员提供生物活性分子抑制剂、激动剂、特异性抑制剂、化合物库、重组蛋白,专注于信号通路和疾病研究领域。

Tubulysin IM-3 

Tubulysin IM-3 是ADC 细胞毒素 (ADC Cytotoxin), 也是一种微管蛋白结合剂,用作抗微管毒素 (anti-microtubule toxins)。

Tubulysin IM-3

Tubulysin IM-3 Chemical Structure

CAS No. : 1639986-05-2

规格 是否有货
100 mg   询价  
250 mg   询价  
500 mg   询价  

* Please select Quantity before adding items.

生物活性

Tubulysin IM-3 is an ADC Cytotoxin and tubulin binder used as anti-microtubule toxins.

IC50 & Target

Traditional Cytotoxic Agents

 

分子量

235.32

Formula

C14H21NO2

CAS 号

1639986-05-2

运输条件

Room temperature in continental US; may vary elsewhere.

储存方式

Please store the product under the recommended conditions in the Certificate of Analysis.

参考文献
  • [1]. EGFR ANTIBODY-BASED COMBINATION THERAPY. Oct 30, 2015

所有产品仅用作科学研究或药证申报,我们不为任何个人用途提供产品和服务

Tubulysin IM-3

上海金畔生物科技有限公司为生命科学和医药研发人员提供生物活性分子抑制剂、激动剂、特异性抑制剂、化合物库、重组蛋白,专注于信号通路和疾病研究领域。

Tubulysin IM-3 

Tubulysin IM-3 是ADC 细胞毒素 (ADC Cytotoxin), 也是一种微管蛋白结合剂,用作抗微管毒素 (anti-microtubule toxins)。

Tubulysin IM-3

Tubulysin IM-3 Chemical Structure

CAS No. : 1639986-05-2

规格 是否有货
100 mg   询价  
250 mg   询价  
500 mg   询价  

* Please select Quantity before adding items.

生物活性

Tubulysin IM-3 is an ADC Cytotoxin and tubulin binder used as anti-microtubule toxins.

IC50 & Target

Traditional Cytotoxic Agents

 

分子量

235.32

Formula

C14H21NO2

CAS 号

1639986-05-2

运输条件

Room temperature in continental US; may vary elsewhere.

储存方式

Please store the product under the recommended conditions in the Certificate of Analysis.

参考文献
  • [1]. EGFR ANTIBODY-BASED COMBINATION THERAPY. Oct 30, 2015

所有产品仅用作科学研究或药证申报,我们不为任何个人用途提供产品和服务

Tubulysin IM-3

上海金畔生物科技有限公司为生命科学和医药研发人员提供生物活性分子抑制剂、激动剂、特异性抑制剂、化合物库、重组蛋白,专注于信号通路和疾病研究领域。

Tubulysin IM-3 

Tubulysin IM-3 是ADC 细胞毒素 (ADC Cytotoxin), 也是一种微管蛋白结合剂,用作抗微管毒素 (anti-microtubule toxins)。

Tubulysin IM-3

Tubulysin IM-3 Chemical Structure

CAS No. : 1639986-05-2

规格 是否有货
100 mg   询价  
250 mg   询价  
500 mg   询价  

* Please select Quantity before adding items.

生物活性

Tubulysin IM-3 is an ADC Cytotoxin and tubulin binder used as anti-microtubule toxins.

IC50 & Target

Traditional Cytotoxic Agents

 

分子量

235.32

Formula

C14H21NO2

CAS 号

1639986-05-2

运输条件

Room temperature in continental US; may vary elsewhere.

储存方式

Please store the product under the recommended conditions in the Certificate of Analysis.

参考文献
  • [1]. EGFR ANTIBODY-BASED COMBINATION THERAPY. Oct 30, 2015

所有产品仅用作科学研究或药证申报,我们不为任何个人用途提供产品和服务

颗粒制冰机IM-25/IM-50/IM-80/IM-100/IM-120

【简单介绍】

颗粒制冰机IM-25/IM-50/IM-80/IM-100/IM-120,全电脑程序控制,制冰速度快、效率高,操作简便。不锈钢外壳,防腐耐用,外观简洁大方,自来水自动进水。

【详细说明】

颗粒制冰机IM-25/IM-50/IM-80/IM-100/IM-120

主要特点:

1) 不锈钢外壳,防腐耐用,外观简洁大方,自来水自动进水。
2) 全电脑程序控制,制冰速度快、效率高,操作简便。
3) 圆柱颗粒形冰,冰粒规整美观,透明程度好。
4) 有冰满和缺水自动停机功能,通过欧洲CE认证。 
5) 高效无氟压缩机,经济节能。

颗粒制冰机IM-25/IM-50/IM-80/IM-100/IM-120

型号参数:

型 号 IM-25
制冰量 (kg/24h) 25
储冰量 (kg) 6
压缩机/制冷剂 进口无氟/R134a
箱体外壳 不锈钢
输入功率(w) 240
箱体外形尺寸 (长X宽X高)(mm) 380X543X672
包装外净尺寸 (长X宽X高)(mm) 457×621×720
净 重(Kg) 30
20’HQ (Pcs) 135
40’HQ (Pcs) 285
冰  型 圆柱颗粒形冰
(直径2.5cm,长度3.5cm)
适用场合 宾馆、饭店、酒吧、KTV

型 号 IM-50
制冰量 (kg/24h) 50
储冰量 (kg) 13
压缩机/制冷剂 进口无氟/R134a
箱体外壳 不锈钢
输入功率(w) 380
箱体外形尺寸 (长X宽X高)(mm) 548X611X833
包装外净尺寸 (长X宽X高)(mm) 625×690×882
净 重(Kg) 47
20’HQ (Pcs) 54
40’HQ (Pcs) 171
冰  型 圆柱颗粒形冰
(直径2.5cm,长度3.5cm)
适用场合 宾馆、饭店、酒吧、KTV

 

型 号 IM-80
制冰量 (kg/24h) 80
储冰量 (kg) 16
压缩机/制冷剂 进口无氟/R134a
箱体外壳 不锈钢
输入功率(w) 650
箱体外形尺寸 (长X宽X高)(mm) 635X611X895
包装外净尺寸 (长X宽X高)(mm) 712×690×944
净 重(Kg) 58
20’HQ (Pcs) 62
40’HQ (Pcs) 171
冰  型 圆柱颗粒形冰
(直径2.5cm,长度3.5cm)
适用场合 宾馆、饭店、酒吧、KTV

型 号 IM-100
制冰量 (kg/24h) 100
储冰量 (kg) 55
压缩机/制冷剂 进口无氟/R134a
箱体外壳 不锈钢
输入功率(w) 680
箱体外形尺寸 (长X宽X高)(mm) 680X611X1050
包装外净尺寸 (长X宽X高)(mm) 755×690×1100
净 重(Kg) 70
20’HQ (Pcs) 62
40’HQ (Pcs) 171
冰  型 圆柱颗粒形冰
(直径2.5cm,长度3.5cm)
适用场合 宾馆、饭店、酒吧、KTV

 

型 号 IM-120
制冰量 (kg/24h) 120
储冰量 (kg) 55
压缩机/制冷剂 进口无氟/R134a
箱体外壳 不锈钢
输入功率(w) 750
箱体外形尺寸 (长X宽X高)(mm) 680X611X1050
包装外净尺寸 (长X宽X高)(mm) 755×690×110
净 重(Kg) 72
20’HQ (Pcs) 62
40’HQ (Pcs) 171
冰  型 圆柱颗粒形冰
(直径2.5cm,长度3.5cm)
适用场合 宾馆、饭店、酒吧、KTV