MNK/PIM-IN-1

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。

MNK/PIM-IN-1 

MNK/PIM-IN-1 是一种新型的 MNK/PIM 双抑制剂,具有良好的药代动力学特征。

MNK/PIM-IN-1

MNK/PIM-IN-1 Chemical Structure

CAS No. : 2430792-91-7

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

MNK/PIM-IN-1 represents an innovative dual MNK/PIM inhibitor with a good pharmacokinetic profile.

分子量

486.54

Formula

C27H27FN6O2

CAS 号

2430792-91-7

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]. Han Y, et al. Optimization of 4,6-Disubstituted Pyrido[3,2-d]pyrimidines as Dual MNK/PIM Inhibitors to Inhibit Leukemia Cell Growth. J Med Chem. 2021 Sep 23;64(18):13719-13735.

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

MNK/PIM-IN-1

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。

MNK/PIM-IN-1 

MNK/PIM-IN-1 是一种新型的 MNK/PIM 双抑制剂,具有良好的药代动力学特征。

MNK/PIM-IN-1

MNK/PIM-IN-1 Chemical Structure

CAS No. : 2430792-91-7

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

MNK/PIM-IN-1 represents an innovative dual MNK/PIM inhibitor with a good pharmacokinetic profile.

分子量

486.54

Formula

C27H27FN6O2

CAS 号

2430792-91-7

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]. Han Y, et al. Optimization of 4,6-Disubstituted Pyrido[3,2-d]pyrimidines as Dual MNK/PIM Inhibitors to Inhibit Leukemia Cell Growth. J Med Chem. 2021 Sep 23;64(18):13719-13735.

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

MNK/PIM-IN-1

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。

MNK/PIM-IN-1 

MNK/PIM-IN-1 是一种新型的 MNK/PIM 双抑制剂,具有良好的药代动力学特征。

MNK/PIM-IN-1

MNK/PIM-IN-1 Chemical Structure

CAS No. : 2430792-91-7

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

MNK/PIM-IN-1 represents an innovative dual MNK/PIM inhibitor with a good pharmacokinetic profile.

分子量

486.54

Formula

C27H27FN6O2

CAS 号

2430792-91-7

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]. Han Y, et al. Optimization of 4,6-Disubstituted Pyrido[3,2-d]pyrimidines as Dual MNK/PIM Inhibitors to Inhibit Leukemia Cell Growth. J Med Chem. 2021 Sep 23;64(18):13719-13735.

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

MNK1/2-IN-5

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。

MNK1/2-IN-5 

MNK1/2-IN-5 是一种有效且选择性的 MNK1/2 抑制剂,可作为治疗剂。

MNK1/2-IN-5

MNK1/2-IN-5 Chemical Structure

CAS No. : 1426928-20-2

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

MNK1/2-IN-5 is a potent and selective MNK1/2 inhibitor as a therapeutic agent.

分子量

308.33

Formula

C17H16N4O2

CAS 号

1426928-20-2

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]. Xu W, et al. Update on the Development of MNK Inhibitors as Therapeutic Agents. J Med Chem. 2021 Sep 17.

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

MNK1/2-IN-5

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。

MNK1/2-IN-5 

MNK1/2-IN-5 是一种有效且选择性的 MNK1/2 抑制剂,可作为治疗剂。

MNK1/2-IN-5

MNK1/2-IN-5 Chemical Structure

CAS No. : 1426928-20-2

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

MNK1/2-IN-5 is a potent and selective MNK1/2 inhibitor as a therapeutic agent.

分子量

308.33

Formula

C17H16N4O2

CAS 号

1426928-20-2

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]. Xu W, et al. Update on the Development of MNK Inhibitors as Therapeutic Agents. J Med Chem. 2021 Sep 17.

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

MNK1/2-IN-5

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。

MNK1/2-IN-5 

MNK1/2-IN-5 是一种有效且选择性的 MNK1/2 抑制剂,可作为治疗剂。

MNK1/2-IN-5

MNK1/2-IN-5 Chemical Structure

CAS No. : 1426928-20-2

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

MNK1/2-IN-5 is a potent and selective MNK1/2 inhibitor as a therapeutic agent.

分子量

308.33

Formula

C17H16N4O2

CAS 号

1426928-20-2

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]. Xu W, et al. Update on the Development of MNK Inhibitors as Therapeutic Agents. J Med Chem. 2021 Sep 17.

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

MNK1/2-IN-6

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。

MNK1/2-IN-6 

MNK1/2-IN-6 是一种有效的选择性的 MNK1/2 抑制剂,IC50s 分别为 2.3 nM 和 3.4 nM。 MNK1/2-IN-6 以浓度依赖性方式诱导细胞凋亡 apoptosis

MNK1/2-IN-6

MNK1/2-IN-6 Chemical Structure

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

MNK1/2-IN-6 is a potent and selective MNK1/2 inhibitor with IC50s of 2.3 nM and 3.4 nM for MNK1 and MNK2, respectively. MNK1/2-IN-6 induces apoptosis in a concentration-dependent manner[1].

IC50 & Target[1]

MNK1

2.3 nM (IC50)

MNK2

3.4 nM (IC50)

体外研究
(In Vitro)

MNK1/2-IN-6 (compound II-5) (72 h) shows antiproliferative activity with IC50s of 0.3896µM, 0.4092 µM for TMD-8, DOHH-2 cells, respectively[1].
MNK1/2-IN-6 (0.25, 0.5, 1 µM; 24 h) induces TMD-8 cells apoptosis in a concentration-dependent manner[1].

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

Cell Proliferation Assay[1]

Cell Line: TMD-8, DOHH-2 cells
Concentration:
Incubation Time: 72 h
Result: Showed antiproliferative activity with IC50s of 0.39µM, 0.41 µM for TMD-8, DOHH-2 cells, respectively.

Apoptosis Analysis[1]

Cell Line: TMD-8 cells
Concentration: 0.25, 0.5, 1 µM
Incubation Time: 24 h
Result: Induced TMD-8 cells apoptosis in a concentration-dependent manner.

分子量

448.52

Formula

C27H24N6O

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]. Bu H, et al. Design, synthesis and biological evaluation of imidazopyridazine derivatives containing isoquinoline group as potent MNK1/2 inhibitors. Bioorg Med Chem. 2021; 40:116186.

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

MNK1/2-IN-6

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。

MNK1/2-IN-6 

MNK1/2-IN-6 是一种有效的选择性的 MNK1/2 抑制剂,IC50s 分别为 2.3 nM 和 3.4 nM。 MNK1/2-IN-6 以浓度依赖性方式诱导细胞凋亡 apoptosis

MNK1/2-IN-6

MNK1/2-IN-6 Chemical Structure

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

MNK1/2-IN-6 is a potent and selective MNK1/2 inhibitor with IC50s of 2.3 nM and 3.4 nM for MNK1 and MNK2, respectively. MNK1/2-IN-6 induces apoptosis in a concentration-dependent manner[1].

IC50 & Target[1]

MNK1

2.3 nM (IC50)

MNK2

3.4 nM (IC50)

体外研究
(In Vitro)

MNK1/2-IN-6 (compound II-5) (72 h) shows antiproliferative activity with IC50s of 0.3896µM, 0.4092 µM for TMD-8, DOHH-2 cells, respectively[1].
MNK1/2-IN-6 (0.25, 0.5, 1 µM; 24 h) induces TMD-8 cells apoptosis in a concentration-dependent manner[1].

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

Cell Proliferation Assay[1]

Cell Line: TMD-8, DOHH-2 cells
Concentration:
Incubation Time: 72 h
Result: Showed antiproliferative activity with IC50s of 0.39µM, 0.41 µM for TMD-8, DOHH-2 cells, respectively.

Apoptosis Analysis[1]

Cell Line: TMD-8 cells
Concentration: 0.25, 0.5, 1 µM
Incubation Time: 24 h
Result: Induced TMD-8 cells apoptosis in a concentration-dependent manner.

分子量

448.52

Formula

C27H24N6O

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]. Bu H, et al. Design, synthesis and biological evaluation of imidazopyridazine derivatives containing isoquinoline group as potent MNK1/2 inhibitors. Bioorg Med Chem. 2021; 40:116186.

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

MNK1/2-IN-6

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。

MNK1/2-IN-6 

MNK1/2-IN-6 是一种有效的选择性的 MNK1/2 抑制剂,IC50s 分别为 2.3 nM 和 3.4 nM。 MNK1/2-IN-6 以浓度依赖性方式诱导细胞凋亡 apoptosis

MNK1/2-IN-6

MNK1/2-IN-6 Chemical Structure

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

MNK1/2-IN-6 is a potent and selective MNK1/2 inhibitor with IC50s of 2.3 nM and 3.4 nM for MNK1 and MNK2, respectively. MNK1/2-IN-6 induces apoptosis in a concentration-dependent manner[1].

IC50 & Target[1]

MNK1

2.3 nM (IC50)

MNK2

3.4 nM (IC50)

体外研究
(In Vitro)

MNK1/2-IN-6 (compound II-5) (72 h) shows antiproliferative activity with IC50s of 0.3896µM, 0.4092 µM for TMD-8, DOHH-2 cells, respectively[1].
MNK1/2-IN-6 (0.25, 0.5, 1 µM; 24 h) induces TMD-8 cells apoptosis in a concentration-dependent manner[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.

Cell Proliferation Assay[1]

Cell Line: TMD-8, DOHH-2 cells
Concentration:
Incubation Time: 72 h
Result: Showed antiproliferative activity with IC50s of 0.39µM, 0.41 µM for TMD-8, DOHH-2 cells, respectively.

Apoptosis Analysis[1]

Cell Line: TMD-8 cells
Concentration: 0.25, 0.5, 1 µM
Incubation Time: 24 h
Result: Induced TMD-8 cells apoptosis in a concentration-dependent manner.

分子量

448.52

Formula

C27H24N6O

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]. Bu H, et al. Design, synthesis and biological evaluation of imidazopyridazine derivatives containing isoquinoline group as potent MNK1/2 inhibitors. Bioorg Med Chem. 2021; 40:116186.

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