标签归档：eda

Biotin-EDA

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。

Biotin-EDA 

Biotin-EDA 是一种 PROTAC linker，属于 alkyl chain 类。可用于合成 PROTAC 分子。

Biotin-EDA

Biotin-EDA Chemical Structure

CAS No. : 111790-37-5

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

Biotin-EDA is an alkyl chain-based PROTAC linker that can be used in the synthesis of PROTACs[1].

IC50 & Target

Alkyl-Chain

 

体外研究
(In Vitro)

PROTACs contain two different ligands connected by a linker; one is a ligand for an E3 ubiquitin ligase and the other is for the target protein. PROTACs exploit the intracellular ubiquitin-proteasome system to selectively degrade target proteins[1].

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

286.39

Formula

C12H22N4O2S
CAS 号

111790-37-5
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]. An S, et al. Small-molecule PROTACs: An emerging and promising approach for the development of targeted therapy drugs. EBioMedicine. 2018 Oct;36:553-562

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

Biotin-EDA

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。

Biotin-EDA 

Biotin-EDA 是一种 PROTAC linker，属于 alkyl chain 类。可用于合成 PROTAC 分子。

Biotin-EDA

Biotin-EDA Chemical Structure

CAS No. : 111790-37-5

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

Biotin-EDA is an alkyl chain-based PROTAC linker that can be used in the synthesis of PROTACs[1].

IC50 & Target

Alkyl-Chain

 

体外研究
(In Vitro)

PROTACs contain two different ligands connected by a linker; one is a ligand for an E3 ubiquitin ligase and the other is for the target protein. PROTACs exploit the intracellular ubiquitin-proteasome system to selectively degrade target proteins[1].

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

286.39

Formula

C12H22N4O2S
CAS 号

111790-37-5
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]. An S, et al. Small-molecule PROTACs: An emerging and promising approach for the development of targeted therapy drugs. EBioMedicine. 2018 Oct;36:553-562

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

PNU-EDA-Gly5

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。

PNU-EDA-Gly5 

PNU-EDA-Gly5 是用于ADC 合成的低聚甘氨酸毒素分子偶联物，由 DNA 拓扑异构酶 I 抑制剂 PNU-159682 和 EDA-Gly5 里连接子组成。

PNU-EDA-Gly5

PNU-EDA-Gly5 Chemical Structure

CAS No. : 1957223-28-7

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

PNU-EDA-Gly5 is an oligo-glycine linker-payload for ADC synthesis, composed of a DNA topoisomerase I inhibitor PNU-159682 and a linker EDA-Gly5[1].

分子量

954.93

Formula

C43H54N8O17
CAS 号

1957223-28-7
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]. Quintieri L, et al. Formation and antitumor activity of PNU-159682, a major metabolite of nemorubicin in human liver microsomes. Clin Cancer Res. 2005 Feb 15;11(4):1608-17.

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

PNU-EDA-Gly5

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。

PNU-EDA-Gly5 

PNU-EDA-Gly5 是用于ADC 合成的低聚甘氨酸毒素分子偶联物，由 DNA 拓扑异构酶 I 抑制剂 PNU-159682 和 EDA-Gly5 里连接子组成。

PNU-EDA-Gly5

PNU-EDA-Gly5 Chemical Structure

CAS No. : 1957223-28-7

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

PNU-EDA-Gly5 is an oligo-glycine linker-payload for ADC synthesis, composed of a DNA topoisomerase I inhibitor PNU-159682 and a linker EDA-Gly5[1].

分子量

954.93

Formula

C43H54N8O17
CAS 号

1957223-28-7
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]. Quintieri L, et al. Formation and antitumor activity of PNU-159682, a major metabolite of nemorubicin in human liver microsomes. Clin Cancer Res. 2005 Feb 15;11(4):1608-17.

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

PNU-EDA-Gly5

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。

PNU-EDA-Gly5 

PNU-EDA-Gly5 是用于ADC 合成的低聚甘氨酸毒素分子偶联物，由 DNA 拓扑异构酶 I 抑制剂 PNU-159682 和 EDA-Gly5 里连接子组成。

PNU-EDA-Gly5

PNU-EDA-Gly5 Chemical Structure

CAS No. : 1957223-28-7

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

PNU-EDA-Gly5 is an oligo-glycine linker-payload for ADC synthesis, composed of a DNA topoisomerase I inhibitor PNU-159682 and a linker EDA-Gly5[1].

分子量

954.93

Formula

C43H54N8O17
CAS 号

1957223-28-7
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]. Quintieri L, et al. Formation and antitumor activity of PNU-159682, a major metabolite of nemorubicin in human liver microsomes. Clin Cancer Res. 2005 Feb 15;11(4):1608-17.

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