标签归档：rest

SCP1-IN-1

发表于由

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。

SCP1-IN-1 

SCP1-IN-1 (compound SH T-62) 是一种针对 SCP1 的强效选择性共价抑制剂。SCP1-IN-1 促进 REST 降解并降低转录活性。高水平的 REST 蛋白驱动一些胶质母细胞瘤细胞的肿瘤生长。SCP1-IN-1 具有研究由 REST 转录活动驱动生长的胶质母细胞瘤的潜力。

SCP1-IN-1

SCP1-IN-1 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

SCP1-IN-1 (compound SH T-62) is a potent and selective covalent inhibitor against SCP1. SCP1-IN-1 promotes REST degradation and reduces transcriptional activity. A high level of REST protein drives the tumor growth in some glioblastoma cells. SCP1-IN-1 has the potential for the research of glioblastoma whose growth is driven by REST transcription activity[1].

分子量

520.50

Formula

C20H19F3N2O7S2
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]. Medellin B, et al. Targeted Covalent Inhibition of Small CTD Phosphatase 1 to Promote the Degradation of the REST Transcription Factor in Human Cells. J Med Chem. 2022;65(1):507-519.

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

SCP1-IN-2

发表于由

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。

SCP1-IN-2 

SCP1-IN-2 (Compound SH T-65) 是一种针对 SCP1 的强效选择性共价抑制剂。SCP1-IN-2 促进 REST 降解并降低转录活性。高水平的 REST 蛋白驱动一些胶质母细胞瘤细胞的肿瘤生长。SCP1-IN-2 具有研究由 REST 转录活动驱动生长的胶质母细胞瘤的潜力。

SCP1-IN-2

SCP1-IN-2 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

SCP1-IN-2 (Compound SH T-65) is a potent and selective covalent inhibitor against SCP1. SCP1-IN-2 promotes REST degradation and reduces transcriptional activity. A high level of REST protein drives the tumor growth in some glioblastoma cells. SCP1-IN-2 has the potential for the research of glioblastoma whose growth is driven by REST transcription activity[1].

分子量

490.47

Formula

C19H17F3N2O6S2
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]. Medellin B, et al. Targeted Covalent Inhibition of Small CTD Phosphatase 1 to Promote the Degradation of the REST Transcription Factor in Human Cells. J Med Chem. 2022;65(1):507-519.

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

SCP1-IN-1

发表于由

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。

SCP1-IN-1 

SCP1-IN-1 (compound SH T-62) 是一种针对 SCP1 的强效选择性共价抑制剂。SCP1-IN-1 促进 REST 降解并降低转录活性。高水平的 REST 蛋白驱动一些胶质母细胞瘤细胞的肿瘤生长。SCP1-IN-1 具有研究由 REST 转录活动驱动生长的胶质母细胞瘤的潜力。

SCP1-IN-1

SCP1-IN-1 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

SCP1-IN-1 (compound SH T-62) is a potent and selective covalent inhibitor against SCP1. SCP1-IN-1 promotes REST degradation and reduces transcriptional activity. A high level of REST protein drives the tumor growth in some glioblastoma cells. SCP1-IN-1 has the potential for the research of glioblastoma whose growth is driven by REST transcription activity[1].

分子量

520.50

Formula

C20H19F3N2O7S2
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]. Medellin B, et al. Targeted Covalent Inhibition of Small CTD Phosphatase 1 to Promote the Degradation of the REST Transcription Factor in Human Cells. J Med Chem. 2022;65(1):507-519.

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

SCP1-IN-2

发表于由

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。

SCP1-IN-2 

SCP1-IN-2 (Compound SH T-65) 是一种针对 SCP1 的强效选择性共价抑制剂。SCP1-IN-2 促进 REST 降解并降低转录活性。高水平的 REST 蛋白驱动一些胶质母细胞瘤细胞的肿瘤生长。SCP1-IN-2 具有研究由 REST 转录活动驱动生长的胶质母细胞瘤的潜力。

SCP1-IN-2

SCP1-IN-2 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

SCP1-IN-2 (Compound SH T-65) is a potent and selective covalent inhibitor against SCP1. SCP1-IN-2 promotes REST degradation and reduces transcriptional activity. A high level of REST protein drives the tumor growth in some glioblastoma cells. SCP1-IN-2 has the potential for the research of glioblastoma whose growth is driven by REST transcription activity[1].

分子量

490.47

Formula

C19H17F3N2O6S2
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]. Medellin B, et al. Targeted Covalent Inhibition of Small CTD Phosphatase 1 to Promote the Degradation of the REST Transcription Factor in Human Cells. J Med Chem. 2022;65(1):507-519.

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

SCP1-IN-1

发表于由

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。

SCP1-IN-1 

SCP1-IN-1 (compound SH T-62) 是一种针对 SCP1 的强效选择性共价抑制剂。SCP1-IN-1 促进 REST 降解并降低转录活性。高水平的 REST 蛋白驱动一些胶质母细胞瘤细胞的肿瘤生长。SCP1-IN-1 具有研究由 REST 转录活动驱动生长的胶质母细胞瘤的潜力。

SCP1-IN-1

SCP1-IN-1 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

SCP1-IN-1 (compound SH T-62) is a potent and selective covalent inhibitor against SCP1. SCP1-IN-1 promotes REST degradation and reduces transcriptional activity. A high level of REST protein drives the tumor growth in some glioblastoma cells. SCP1-IN-1 has the potential for the research of glioblastoma whose growth is driven by REST transcription activity[1].

分子量

520.50

Formula

C20H19F3N2O7S2
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]. Medellin B, et al. Targeted Covalent Inhibition of Small CTD Phosphatase 1 to Promote the Degradation of the REST Transcription Factor in Human Cells. J Med Chem. 2022;65(1):507-519.

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

SCP1-IN-2

发表于由

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。

SCP1-IN-2 

SCP1-IN-2 (Compound SH T-65) 是一种针对 SCP1 的强效选择性共价抑制剂。SCP1-IN-2 促进 REST 降解并降低转录活性。高水平的 REST 蛋白驱动一些胶质母细胞瘤细胞的肿瘤生长。SCP1-IN-2 具有研究由 REST 转录活动驱动生长的胶质母细胞瘤的潜力。

SCP1-IN-2

SCP1-IN-2 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

SCP1-IN-2 (Compound SH T-65) is a potent and selective covalent inhibitor against SCP1. SCP1-IN-2 promotes REST degradation and reduces transcriptional activity. A high level of REST protein drives the tumor growth in some glioblastoma cells. SCP1-IN-2 has the potential for the research of glioblastoma whose growth is driven by REST transcription activity[1].

分子量

490.47

Formula

C19H17F3N2O6S2
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]. Medellin B, et al. Targeted Covalent Inhibition of Small CTD Phosphatase 1 to Promote the Degradation of the REST Transcription Factor in Human Cells. J Med Chem. 2022;65(1):507-519.

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