标签归档：conh

DBCO-CONH-S-S-NHS ester

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。

DBCO-CONH-S-S-NHS ester  纯度: 95.04%

DBCO-CONH-S-S-NHS ester 是一种可降解 (cleavable) 的 ADC linker，可用于合成抗体偶联药物 (ADC)。

DBCO-CONH-S-S-NHS ester

DBCO-CONH-S-S-NHS ester Chemical Structure

CAS No. : 1435934-53-4

规格 价格 是否有货 数量
25 mg ￥6500 In-stock
50 mg ￥9500 询价
100 mg ￥13500 询价
200 mg   询价  
500 mg   询价  

* Please select Quantity before adding items.

生物活性

DBCO-CONH-S-S-NHS ester is a cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs)[1].

IC50 & Target

Cleavable

 

体外研究
(In Vitro)

ADCs are comprised of an antibody to which is attached an ADC cytotoxin through an ADC linker[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.
分子量

565.66

Formula

C28H27N3O6S2
CAS 号

1435934-53-4
运输条件

Room temperature in continental US; may vary elsewhere.
储存方式

4°C, protect from light, stored under nitrogen

*In solvent : -80°C, 6 months; -20°C, 1 month (protect from light, stored under nitrogen)
参考文献

  • [1]. Beck A, et al. Strategies and challenges for the next generation of antibody-drug conjugates. Nat Rev Drug Discov. 2017 May;16(5):315-337.

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

Amino-PEG36-CONH-PEG36-acid

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。

Amino-PEG36-CONH-PEG36-acid 

Amino-PEG36-CONH-PEG36-acid 是一种 PROTAC linker，属于 PEG 类。可用于合成 PROTAC 分子。

Amino-PEG36-CONH-PEG36-acid

Amino-PEG36-CONH-PEG36-acid 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

Amino-PEG36-CONH-PEG36-acid is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs[1].

IC50 & Target

PEGs

 

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

3331.99

Formula

C10H20N2O5
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

Amino-PEG36-CONH-PEG36-acid

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。

Amino-PEG36-CONH-PEG36-acid 

Amino-PEG36-CONH-PEG36-acid 是一种 PROTAC linker，属于 PEG 类。可用于合成 PROTAC 分子。

Amino-PEG36-CONH-PEG36-acid

Amino-PEG36-CONH-PEG36-acid 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

Amino-PEG36-CONH-PEG36-acid is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs[1].

IC50 & Target

PEGs

 

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

3331.99

Formula

C10H20N2O5
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

Mal-Ph-CONH-PEG4-​NHS ester

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。

Mal-Ph-CONH-PEG4-​NHS ester 

Mal-Ph-CONH-PEG4-​NHS ester 是一种不可降解 (non-cleavable) 的含 4 个单元 PEG 的 ADC linker，可用于合成抗体偶联药物 (ADC)。

Mal-Ph-CONH-PEG4-​NHS ester

Mal-Ph-CONH-PEG4-​NHS ester Chemical Structure

CAS No. : 1263044-88-7

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

Mal-Ph-CONH-PEG4-​NHS ester is a non-cleavable 4 unit PEG ADC linker used in the synthesis of antibody-drug conjugates (ADCs)[1].

IC50 & Target

Non-cleavable

 

体外研究
(In Vitro)

ADCs are comprised of an antibody to which is attached an ADC cytotoxin through an ADC linker[1].

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

561.54

Formula

C26H31N3O11
CAS 号

1263044-88-7
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]. Beck A, et al. Strategies and challenges for the next generation of antibody-drug conjugates. Nat Rev Drug Discov. 2017 May;16(5):315-337.

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

Mal-Ph-CONH-PEG4-​NHS ester

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。

Mal-Ph-CONH-PEG4-​NHS ester 

Mal-Ph-CONH-PEG4-​NHS ester 是一种不可降解 (non-cleavable) 的含 4 个单元 PEG 的 ADC linker，可用于合成抗体偶联药物 (ADC)。

Mal-Ph-CONH-PEG4-​NHS ester

Mal-Ph-CONH-PEG4-​NHS ester Chemical Structure

CAS No. : 1263044-88-7

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

Mal-Ph-CONH-PEG4-​NHS ester is a non-cleavable 4 unit PEG ADC linker used in the synthesis of antibody-drug conjugates (ADCs)[1].

IC50 & Target

Non-cleavable

 

体外研究
(In Vitro)

ADCs are comprised of an antibody to which is attached an ADC cytotoxin through an ADC linker[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.
分子量

561.54

Formula

C26H31N3O11
CAS 号

1263044-88-7
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]. Beck A, et al. Strategies and challenges for the next generation of antibody-drug conjugates. Nat Rev Drug Discov. 2017 May;16(5):315-337.

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

Mal-Ph-CONH-PEG4-​NHS ester

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。

Mal-Ph-CONH-PEG4-​NHS ester 

Mal-Ph-CONH-PEG4-​NHS ester 是一种不可降解 (non-cleavable) 的含 4 个单元 PEG 的 ADC linker，可用于合成抗体偶联药物 (ADC)。

Mal-Ph-CONH-PEG4-​NHS ester

Mal-Ph-CONH-PEG4-​NHS ester Chemical Structure

CAS No. : 1263044-88-7

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

Mal-Ph-CONH-PEG4-​NHS ester is a non-cleavable 4 unit PEG ADC linker used in the synthesis of antibody-drug conjugates (ADCs)[1].

IC50 & Target

Non-cleavable

 

体外研究
(In Vitro)

ADCs are comprised of an antibody to which is attached an ADC cytotoxin through an ADC linker[1].

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

561.54

Formula

C26H31N3O11
CAS 号

1263044-88-7
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]. Beck A, et al. Strategies and challenges for the next generation of antibody-drug conjugates. Nat Rev Drug Discov. 2017 May;16(5):315-337.

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

HOE 33187-O-CONH-PEG4-phenol-thiophenone-NHPh-COOEt

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。

HOE 33187-O-CONH-PEG4-phenol-thiophenone-NHPh-COOEt 

HOE 33187-O-CONH-PEG4-phenol-thiophenone-NHPh-COOEt 对pre-miR-21 RNA 具有抑制活性。HOE 33187-O-CONH-PEG4-phenol-thiophenone-NHPh-COOEt 具有研究肿瘤疾病的潜力，例如癌症，尤其是表达 miR-21 的癌症 (信息提取自专利 2021087084A1，compound 25)。

HOE 33187-O-CONH-PEG4-phenol-thiophenone-NHPh-COOEt

HOE 33187-O-CONH-PEG4-phenol-thiophenone-NHPh-COOEt Chemical Structure

CAS No. : 2641500-83-4

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

HOE 33187-O-CONH-PEG4-phenol-thiophenone-NHPh-COOEt has inhibitory activity against pre-miR-21 RNA. HOE 33187-O-CONH-PEG4-phenol-thiophenone-NHPh-COOEt has the potential for the research of neoplastic disease such as cancer and especially cancers expressing miR-21 (extracted from patent WO2021087084A1, compound 25)[1].

IC50 & Target

pre-miR-21 RNA[1]
分子量

1051.21

Formula

C57H62N8O10S
CAS 号

2641500-83-4
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]. Matthew D. Disney, et al. COMPOUNDS AND MODULES FOR INHIBITION OF PRE-miR-21 AND THEIR USE IN TREATMENT OF CERTAIN CANCERS. Patent WO2021087084A1.

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

HOE 33187-O-CONH-PEG4-phenol-thiophenone-NHPh-COOEt

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。

HOE 33187-O-CONH-PEG4-phenol-thiophenone-NHPh-COOEt 

HOE 33187-O-CONH-PEG4-phenol-thiophenone-NHPh-COOEt 对pre-miR-21 RNA 具有抑制活性。HOE 33187-O-CONH-PEG4-phenol-thiophenone-NHPh-COOEt 具有研究肿瘤疾病的潜力，例如癌症，尤其是表达 miR-21 的癌症 (信息提取自专利 2021087084A1，compound 25)。

HOE 33187-O-CONH-PEG4-phenol-thiophenone-NHPh-COOEt

HOE 33187-O-CONH-PEG4-phenol-thiophenone-NHPh-COOEt Chemical Structure

CAS No. : 2641500-83-4

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

HOE 33187-O-CONH-PEG4-phenol-thiophenone-NHPh-COOEt has inhibitory activity against pre-miR-21 RNA. HOE 33187-O-CONH-PEG4-phenol-thiophenone-NHPh-COOEt has the potential for the research of neoplastic disease such as cancer and especially cancers expressing miR-21 (extracted from patent WO2021087084A1, compound 25)[1].

IC50 & Target

pre-miR-21 RNA[1]
分子量

1051.21

Formula

C57H62N8O10S
CAS 号

2641500-83-4
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]. Matthew D. Disney, et al. COMPOUNDS AND MODULES FOR INHIBITION OF PRE-miR-21 AND THEIR USE IN TREATMENT OF CERTAIN CANCERS. Patent WO2021087084A1.

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

HOE 33187-O-CONH-PEG4-phenol-thiophenone-NHPh-COOEt

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。

HOE 33187-O-CONH-PEG4-phenol-thiophenone-NHPh-COOEt 

HOE 33187-O-CONH-PEG4-phenol-thiophenone-NHPh-COOEt 对pre-miR-21 RNA 具有抑制活性。HOE 33187-O-CONH-PEG4-phenol-thiophenone-NHPh-COOEt 具有研究肿瘤疾病的潜力，例如癌症，尤其是表达 miR-21 的癌症 (信息提取自专利 2021087084A1，compound 25)。

HOE 33187-O-CONH-PEG4-phenol-thiophenone-NHPh-COOEt

HOE 33187-O-CONH-PEG4-phenol-thiophenone-NHPh-COOEt Chemical Structure

CAS No. : 2641500-83-4

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

HOE 33187-O-CONH-PEG4-phenol-thiophenone-NHPh-COOEt has inhibitory activity against pre-miR-21 RNA. HOE 33187-O-CONH-PEG4-phenol-thiophenone-NHPh-COOEt has the potential for the research of neoplastic disease such as cancer and especially cancers expressing miR-21 (extracted from patent WO2021087084A1, compound 25)[1].

IC50 & Target

pre-miR-21 RNA[1]
分子量

1051.21

Formula

C57H62N8O10S
CAS 号

2641500-83-4
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]. Matthew D. Disney, et al. COMPOUNDS AND MODULES FOR INHIBITION OF PRE-miR-21 AND THEIR USE IN TREATMENT OF CERTAIN CANCERS. Patent WO2021087084A1.

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