Bis-Tos-PEG4(Synonyms: PROTAC Linker 16)

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。

Bis-Tos-PEG4 (Synonyms: PROTAC Linker 16) 纯度: 98.61%

Bis-Tos-PEG4 (PROTAC Linker 16) 是一种 PROTAC linker,属于 PEG 类。Bis-Tos-PEG4 可用于合成 PROTAC 分子。

Bis-Tos-PEG4(Synonyms: PROTAC Linker 16)

Bis-Tos-PEG4 Chemical Structure

CAS No. : 37860-51-8

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生物活性

Bis-Tos-PEG4 (PROTAC Linker 16) is a PEG-based PROTAC linker 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

502.60

Formula

C22H30O9S2

CAS 号

37860-51-8

运输条件

Room temperature in continental US; may vary elsewhere.

储存方式
Pure form -20°C 3 years
4°C 2 years
In solvent -80°C 6 months
-20°C 1 month
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.

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Bis-NH2-C1-PEG3(Synonyms: PROTAC Linker 24)

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。

Bis-NH2-C1-PEG3 (Synonyms: PROTAC Linker 24)

Bis-NH2-C1-PEG3 (PROTAC Linker 24) 是一种 PROTAC linker,属于 PEG 类。Bis-NH2-C1-PEG3 可用于合成 PROTAC 分子。

Bis-NH2-C1-PEG3(Synonyms: PROTAC Linker 24)

Bis-NH2-C1-PEG3 Chemical Structure

CAS No. : 4246-51-9

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生物活性

Bis-NH2-C1-PEG3 (PROTAC Linker 24) is a PEG-based PROTAC linker can be used in the synthesis of PROTACs[1].

IC50 & Target[1]

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

220.31

Formula

C10H24N2O3

CAS 号

4246-51-9

运输条件

Room temperature in continental US; may vary elsewhere.

储存方式

4°C, protect from light

*In solvent : -80°C, 6 months; -20°C, 1 month (protect from light)

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.

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BnOH-NH-bis-(C2-S)-propane-O-isoprene ester(Synonyms: PROTAC Linker 29)

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。

BnOH-NH-bis-(C2-S)-propane-O-isoprene ester (Synonyms: PROTAC Linker 29)

BnOH-NH-bis-(C2-S)-propane-O-isoprene ester (PROTAC Linker 29) 是一种 PROTAC linker,属于 alkyl ether 类。BnOH-NH-bis-(C2-S)-propane-O-isoprene ester 可用于合成 PROTAC 分子。

BnOH-NH-bis-(C2-S)-propane-O-isoprene ester(Synonyms: PROTAC Linker 29)

BnOH-NH-bis-(C2-S)-propane-O-isoprene ester Chemical Structure

CAS No. : 2448704-23-0

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生物活性

BnOH-NH-bis-(C2-S)-propane-O-isoprene ester (PROTAC Linker 29) is an alkyl ether-based PROTAC linker can be used in the synthesis of PROTACs[1].

IC50 & Target

Alkyl/ether

 

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

397.55

Formula

C19H27NO4S2

CAS 号

2448704-23-0

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.

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Bis-​PEG4-​NHS ester

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。

Bis-​PEG4-​NHS ester 

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

Bis-​PEG4-​NHS ester

Bis-​PEG4-​NHS ester Chemical Structure

CAS No. : 1314378-11-4

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生物活性

Bis-​PEG4-​NHS ester is a nonclaevable 4-unit PEG linker for antibody-drug-conjugation (ADC).

IC50 & Target

Non-cleavable

 

分子量

488.44

Formula

C20H28N2O12

CAS 号

1314378-11-4

运输条件

Room temperature in continental US; may vary elsewhere.

储存方式
Powder -20°C 3 years
In solvent -80°C 6 months
-20°C 1 month

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Bis-PEG3-NHS ester

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。

Bis-PEG3-NHS ester 

Bis-PEG3-NHS ester 是一种不可降解的含 3 个单元 PEG 的 linker,可用于合成抗体偶联药物 (ADC) 。

Bis-PEG3-NHS ester

Bis-PEG3-NHS ester Chemical Structure

CAS No. : 1314378-16-9

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生物活性

Bis-PEG3-NHS ester is a nonclaevable 3-unit PEG linker for antibody-drug-conjugation (ADC).

IC50 & Target

Non-cleavable

 

分子量

444.39

Formula

C18H24N2O11

CAS 号

1314378-16-9

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.

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NH-bis(C1-Boc)

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。

NH-bis(C1-Boc) 

Boc-NH-C6-Br 是一种不可降解 (non-cleavable) 的 linker,用于抗体偶联药物 (ADC)。

NH-bis(C1-Boc)

NH-bis(C1-Boc) Chemical Structure

CAS No. : 85916-13-8

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生物活性

NH-bis(C1-Boc)is a uncleavable linker used for antibody-drug conjugates (ADC).

IC50 & Target

Non-cleavable

 

分子量

245.32

Formula

C12H23NO4

CAS 号

85916-13-8

运输条件

Room temperature in continental US; may vary elsewhere.

储存方式

4°C, protect from light

*In solvent : -80°C, 6 months; -20°C, 1 month (protect from light)

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1,2-Bis(2-iodoethoxy)ethane

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。

1,2-Bis(2-iodoethoxy)ethane 

1,2-Bis(2-iodoethoxy)ethane 是一种 PROTAC linker,属于 PEG 类。1,2-Bis(2-iodoethoxy)ethane 可用于合成 MT802 (HY-122562) 和 SJF620 (HY-133137)。MT-802 和 SJF620 都是 PROTAC BTK 降解剂,DC50 分别为 1 和 7.9 nM。

1,2-Bis(2-iodoethoxy)ethane

1,2-Bis(2-iodoethoxy)ethane Chemical Structure

CAS No. : 36839-55-1

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生物活性

1,2-Bis(2-iodoethoxy)ethane is a PEG-based PROTAC linker. 1,2-Bis(2-iodoethoxy)ethane can be used in the synthesis of MT802 (HY-122562) and SJF620 (HY-133137). MT-802 and SJF620 are potent PROTAC BTK degraders with DC50s of 1 nM and 7.9 nM, respectively[1].

IC50 & Target[1]

PEGs

 

体外研究
(In Vitro)

1,2-Bis(2-iodoethoxy)ethane is a PROTAC linker, which refers to the PEG composition. 1,2-Bis(2-iodoethoxy)ethane can be used in the synthesis of a series of PROTACs, such as MT802 (HY-122562) and SJF620 (HY-133137). PROTAC MT802(HY-122562) has a ligand specific for BTK, and a ligand specific to a E3 ligase cereblon (CRBN) connected by polyethylene glycol (PEG) linker 1,2-Bis(2-iodoethoxy)ethane[1].

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

分子量

369.97

Formula

C6H12I2O2

CAS 号

36839-55-1

运输条件

Room temperature in continental US; may vary elsewhere.

储存方式

4°C, protect from light

*In solvent : -80°C, 6 months; -20°C, 1 month (protect from light)

参考文献
  • [1]. Jaime-Figueroa S, et al. Design, synthesis and biological evaluation of Proteolysis Targeting Chimeras (PROTACs) as a BTK degraders with improved pharmacokinetic properties. 2020 Feb 1;30(3):126877.

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NH-bis-PEG2

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。

NH-bis-PEG2 

NH-bis-PEG2 是一种不可裂解 (non-cleavable) 的 2 单元 PEG 的 ADC linker,用于抗体药物偶联物 (ADCs) 的合成。NH-bis-PEG2 也是一种基于 PEG 的 PROTAC linker,可用于 PROTAC 的合成。

NH-bis-PEG2

NH-bis-PEG2 Chemical Structure

CAS No. : 54384-47-3

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生物活性

NH-bis-PEG2 is a non-cleavable 2 unit PEG ADC linker used in the synthesis of antibody-drug conjugates (ADCs). NH-bis-PEG2 is also a PEG-based PROTAC linker that can be used in the synthesis of PROTACs.

IC50 & Target

Non-cleavable

 

PEGs

 

体外研究
(In Vitro)

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

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

分子量

193.24

Formula

C8H19NO4

CAS 号

54384-47-3

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]. Brown A, et al. PEG-lipid micelles enable cholesterol efflux in Niemann-Pick Type C1 disease-based lysosomal storage disorder. Sci Rep. 2016 Aug 30;6:31750.

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Bis-PEG1-PFP ester

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。

Bis-PEG1-PFP ester 

Bis-PEG1-PFP ester是一种不可降解 (non-cleavable) 的含 1 个单元 PEG 的 ADC linker,可用于合成 抗体偶联药物 (ADC)。

Bis-PEG1-PFP ester

Bis-PEG1-PFP ester Chemical Structure

CAS No. : 1807539-02-1

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生物活性

Bis-PEG1-PFP ester is a non-cleavable (1 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.

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

分子量

494.24

Formula

C18H8F10O5

CAS 号

1807539-02-1

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]. CORTEZ, Alex, et al. ANTIBODY CONJUGATES COMPRISING TOLL-LIKE RECEPTOR AGONIST. WO2017072662A1.

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Bis-PEG1-acid

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。

Bis-PEG1-acid 

Bis-PEG1-acid 是一种 PROTAC linker,属于 PEG 类。Bis-PEG1-acid 可用于合成 PROTAC 分子。

Bis-PEG1-acid

Bis-PEG1-acid Chemical Structure

CAS No. : 5961-83-1

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100 mg ¥3500 In-stock
250 mg ¥5950 In-stock
500 mg   询价  
1 g   询价  

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生物活性

Bis-PEG1-acid is a PEG-based PROTAC linker 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

162.14

Formula

C6H10O5

CAS 号

5961-83-1

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.

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N-Bis(2-hydroxypropyl)nitrosamine(Synonyms: DHPN; Di(2-hydroxypropyl)nitrosamine; Diisopropanolnitrosamine)

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。

N-Bis(2-hydroxypropyl)nitrosamine (Synonyms: DHPN; Di(2-hydroxypropyl)nitrosamine; Diisopropanolnitrosamine) 纯度: ≥98.0%

N-Bis(2-hydroxypropyl)nitrosamine 是一种具有致癌作用的试剂。

N-Bis(2-hydroxypropyl)nitrosamine(Synonyms: DHPN;  Di(2-hydroxypropyl)nitrosamine;  Diisopropanolnitrosamine)

N-Bis(2-hydroxypropyl)nitrosamine Chemical Structure

CAS No. : 53609-64-6

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Free Sample (0.1-0.5 mg)   Apply now  
10 mM * 1 mL in DMSO ¥660 In-stock
10 mg ¥600 In-stock
25 mg ¥1200 In-stock
50 mg ¥1900 In-stock
100 mg ¥2900 In-stock
200 mg ¥4900 In-stock
500 mg   询价  
1 g   询价  

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N-Bis(2-hydroxypropyl)nitrosamine 相关产品

相关化合物库:

  • Bioactive Compound Library Plus
  • Anti-Cancer Compound Library

生物活性

N-Bis(2-hydroxypropyl)nitrosamine is an agent with carcinogenic activity.

体外研究
(In Vitro)

N-Bis(2-hydroxypropyl)nitrosamine is an agent with carcinogenic activity[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.

体内研究
(In Vivo)

N-Bis(2-hydroxypropyl)nitrosamine causes the tumors to develop in the lung, liver, and thyroid of rats at a dose of 100 ppm, in the lung, liver thyroid, esophagus, kidney, and urinary bladder of rats at a dose of 500 ppm, and in the lung, liver thyroid, esophagus, kidney, and urinary bladder of rats at both doses[1]. Bisphenol A (BPA) enhances the susceptibility to thyroid carcinoma stimulated by N-Bis(2-hydroxypropyl)nitrosamine (DHPN; 2800 mg/kg) in rats[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.

分子量

162.19

Formula

C6H14N2O3

CAS 号

53609-64-6

运输条件

Room temperature in continental US; may vary elsewhere.

储存方式
Pure form -20°C 3 years
4°C 2 years
In solvent -80°C 6 months
-20°C 1 month
溶解性数据
In Vitro: 

DMSO : ≥ 125 mg/mL (770.70 mM)

* “≥” means soluble, but saturation unknown.

配制储备液
浓度 溶剂体积 质量 1 mg 5 mg 10 mg
1 mM 6.1656 mL 30.8280 mL 61.6561 mL
5 mM 1.2331 mL 6.1656 mL 12.3312 mL
10 mM 0.6166 mL 3.0828 mL 6.1656 mL

*

请根据产品在不同溶剂中的溶解度选择合适的溶剂配制储备液;一旦配成溶液,请分装保存,避免反复冻融造成的产品失效
储备液的保存方式和期限:-80°C, 6 months; -20°C, 1 month。-80°C 储存时,请在 6 个月内使用,-20°C 储存时,请在 1 个月内使用。

参考文献
  • [1]. Konishi Y, et al. Effect of dose on the carcinogenic activity of orally administered N-bis(2-hydroxypropyl)nitrosamine in rats. Gan. 1978 Aug;69(4):573-7.

    [2]. Zhang J, et al. Low dose of Bisphenol A enhance the susceptibility of thyroid carcinoma stimulated by DHPN and iodine excess in F344 rats. Oncotarget. 2017 Jul 22;8(41):69874-69887.

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Bis-propargyl-PEG8

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。

Bis-propargyl-PEG8 

Bis-propargyl-PEG8 (compound 16e) 是一种 PROTAC linker,属于 PEG 类。Bis-propargyl-PEG8 可用于合成一系列 PROTAC 分子。

Bis-propargyl-PEG8

Bis-propargyl-PEG8 Chemical Structure

CAS No. : 1092554-87-4

规格 是否有货
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500 mg   询价  

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生物活性

Bis-propargyl-PEG8 (compound 16e) is a PEG-based PROTAC linker can be used in the synthesis of PROTACs.

IC50 & Target[1]

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.

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

分子量

446.53

Formula

C22H38O9

CAS 号

1092554-87-4

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]. Jervis PJ, et al. Towards multivalent CD1d ligands: synthesis and biological activity of homodimeric α-galactosyl ceramide analogues. Carbohydr Res. 2012 Jul 15;356:152-62.

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N-Boc-N-bis(PEG2-OH)

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。

N-Boc-N-bis(PEG2-OH) 

N-Boc-N-bis(PEG2-OH) 是一种 PROTAC 连接桥,属于 PEG 类和 Alkyl/ether 类。N-Boc-N-bis(PEG2-OH) 可用于合成一系列 PROTAC 分子。N-Boc-N-bis(PEG2-OH) 是一种可降解 (cleavable) 的 ADC 连接桥,用于抗体药物结合物 (ADCs) 的合成。

N-Boc-N-bis(PEG2-OH)

N-Boc-N-bis(PEG2-OH) Chemical Structure

CAS No. : 275385-03-0

规格 是否有货
100 mg   询价  
250 mg   询价  
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生物活性

N-Boc-N-bis(PEG2-OH) is a PEG/Alkyl/ether-based PROTAC linker can be used in the synthesis of PROTACs. N-Boc-N-bis(PEG2-OH) is a cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs)[1].

IC50 & Target[1]

Cleavable

 

PEGs

 

Alkyl/ether

 

体外研究
(In Vitro)

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

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

分子量

293.36

Formula

C13H27NO6

CAS 号

275385-03-0

运输条件

Room temperature in continental US; may vary elsewhere.

储存方式
Pure form -20°C 3 years
4°C 2 years
In solvent -80°C 6 months
-20°C 1 month
参考文献
  • [1]. Deqiang A, et al. Process for preparation of tetramaleimide linker and application. WO2019033773A1.

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N-Boc-N-bis(PEG4-OH)

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。

N-Boc-N-bis(PEG4-OH) 

N-Boc-N-bis(PEG4-OH) 是一种 PROTAC 连接桥,属于 PEG 类。N-Boc-N-bis(PEG4-OH) 可用于合成一系列 PROTAC 分子。N-Boc-N-bis(PEG4-OH) 是一种可降解 (cleavable) 的 ADC 连接桥,用于抗体药物结合物 (ADCs) 的合成。

N-Boc-N-bis(PEG4-OH)

N-Boc-N-bis(PEG4-OH) Chemical Structure

CAS No. : 2093154-01-7

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

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生物活性

N-Boc-N-bis(PEG4-OH) is a PEG-based PROTAC linker can be used in the synthesis of PROTACs. N-Boc-N-bis(PEG4-OH) is a cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs)[1].

IC50 & Target[1]

Cleavable

 

PEGs

 

Alkyl/ether

 

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

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

分子量

469.57

Formula

C21H43NO10

CAS 号

2093154-01-7

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]. Alain Wagner, et al. Intra-droplet surface engineering to capture a molecular target. WO2017174610A1.

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Bis-propargyl-PEG2

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。

Bis-propargyl-PEG2 

Bis-propargyl-PEG2 是一种 PROTAC linker,属于 PEG类,可以用于合成 PROTAC。Bis-propargyl-PEG2 被用于合成去甲万古霉素。

Bis-propargyl-PEG2

Bis-propargyl-PEG2 Chemical Structure

CAS No. : 126422-57-9

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

Bis-propargyl-PEG2 is a PEG-based PROTAC linker can be used in the synthesis of PROTACs. Bis-propargyl-PEG2 is used for the synthesis of demethylvancomycin dimers[1][2].

IC50 & Target

PEGs

 

体外研究
(In Vitro)

Bis-propargyl-PEG2 can be used in the synthesis of demethylvancomycin dimers against vancomycin-resistant enterococcus faecalis[2].

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

分子量

182.22

Formula

C10H14O3

CAS 号

126422-57-9

运输条件

Room temperature in continental US; may vary elsewhere.

储存方式
Pure form -20°C 3 years
4°C 2 years
In solvent -80°C 6 months
-20°C 1 month
参考文献
  • [1]. Shenoi RA, et al. Synthesis, characterization, and biocompatibility of biodegradable hyperbranched polyglycerols from acid-cleavable ketal group functionalized initiators. Biomacromolecules. 2012 Oct 8;13(10):3018-30.

    [2]. Jiang, et al. Design, synthesis and biological activity of novel demethylvancomycin dimers against vancomycin-resistant enterococcus faecalis. Tetrahedron, 2018: 74(27), 3527–3533.

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Bis-propargyl-PEG3

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。

Bis-propargyl-PEG3  纯度: ≥98.0%

Bis-propargyl-PEG3 是一种可以用于合成 PROTAC 的 PROTAC linker,属于 PEG 类。Bis-propargyl-PEG3 可以用于合成具有抗疟原虫活性的 ZnDPA 复合物。

Bis-propargyl-PEG3

Bis-propargyl-PEG3 Chemical Structure

CAS No. : 126422-58-0

规格 价格 是否有货 数量
250 mg ¥1500 In-stock
1 g ¥3500 In-stock
5 g   询价  
10 g   询价  

* Please select Quantity before adding items.

生物活性

Bis-propargyl-PEG3 is a PEG-based PROTAC linker used in the synthesis of PROTACs. Bis-propargyl-PEG3 is used in the synthesis of zinc-dipicolylamine (ZnDPA) complexes with antiplasmodial activity[1] [2].

IC50 & Target

PEGs

 

体外研究
(In Vitro)

Bis-propargyl-PEG3 is used in the synthesis of zinc-dipicolylamine (ZnDPA) complexes with antiplasmodial activity against three strains of Plasmodium falciparum [2].

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

分子量

226.27

Formula

C12H18O4

CAS 号

126422-58-0

运输条件

Room temperature in continental US; may vary elsewhere.

储存方式
Pure form -20°C 3 years
4°C 2 years
In solvent -80°C 6 months
-20°C 1 month
溶解性数据
In Vitro: 

DMSO : 100 mg/mL (441.95 mM; Need ultrasonic)

配制储备液
浓度 溶剂体积 质量 1 mg 5 mg 10 mg
1 mM 4.4195 mL 22.0975 mL 44.1950 mL
5 mM 0.8839 mL 4.4195 mL 8.8390 mL
10 mM 0.4419 mL 2.2097 mL 4.4195 mL

*

请根据产品在不同溶剂中的溶解度选择合适的溶剂配制储备液;一旦配成溶液,请分装保存,避免反复冻融造成的产品失效
储备液的保存方式和期限:-80°C, 6 months; -20°C, 1 month。-80°C 储存时,请在 6 个月内使用,-20°C 储存时,请在 1 个月内使用。

In Vivo:

请根据您的实验动物和给药方式选择适当的溶解方案。以下溶解方案都请先按照 In Vitro 方式配制澄清的储备液,再依次添加助溶剂:

——为保证实验结果的可靠性,澄清的储备液可以根据储存条件,适当保存;体内实验的工作液,建议您现用现配,当天使用; 以下溶剂前显示的百
分比是指该溶剂在您配制终溶液中的体积占比;如在配制过程中出现沉淀、析出现象,可以通过加热和/或超声的方式助溶

  • 1.

    请依序添加每种溶剂: 10% DMSO    40% PEG300    5% Tween-80    45% saline

    Solubility: ≥ 2.5 mg/mL (11.05 mM); Clear solution

    此方案可获得 ≥ 2.5 mg/mL (11.05 mM,饱和度未知) 的澄清溶液。

    以 1 mL 工作液为例,取 100 μL 25.0 mg/mL 的澄清 DMSO 储备液加到 400 μL PEG300 中,混合均匀;向上述体系中加入50 μL Tween-80,混合均匀;然后继续加入 450 μL生理盐水定容至 1 mL。

    将 0.9 g 氯化钠,完全溶解于 100 mL ddH₂O 中,得到澄清透明的生理盐水溶液

  • 2.

    请依序添加每种溶剂: 10% DMSO    90% (20% SBE-β-CD in saline)

    Solubility: ≥ 2.5 mg/mL (11.05 mM); Clear solution

    此方案可获得 ≥ 2.5 mg/mL (11.05 mM,饱和度未知) 的澄清溶液。

    以 1 mL 工作液为例,取 100 μL 25.0 mg/mL 的澄清 DMSO 储备液加到 900 μL 20% 的 SBE-β-CD 生理盐水水溶液中,混合均匀。

    将 2 g 磺丁基醚 β-环糊精加入 5 mL 生理盐水中,再用生理盐水定容至 10 mL,完全溶解,澄清透明
  • 3.

    请依序添加每种溶剂: 10% DMSO    90% corn oil

    Solubility: ≥ 2.5 mg/mL (11.05 mM); Clear solution

    此方案可获得 ≥ 2.5 mg/mL (11.05 mM,饱和度未知) 的澄清溶液,此方案不适用于实验周期在半个月以上的实验。

    以 1 mL 工作液为例,取 100 μL 25.0 mg/mL 的澄清 DMSO 储备液加到 900 μL玉米油中,混合均匀。

*以上所有助溶剂都可在 Shanghai Jinpan Biotech Co Ltd 网站选购。
参考文献
  • [1]. Pearlie BURNETTE, et al. Dimeric immuno-modulatory compounds against cereblon-based mechanisms. WO2020014489A2.

    [2]. Rice DR, et al. Antiplasmodial activity of targeted zinc(II)-dipicolylamine complexes. Bioorg Med Chem. 2017 May 15;25(10):2754-2760.

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

Bis-propargyl-PEG4

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。

Bis-propargyl-PEG4  纯度: 95.64%

Bis-propargyl-PEG4 是一种用于合成 PORTAC 的 PROTAC linker,属于 PEG 类。Bis-propargyl-PEG2 被用于合成去甲万古霉素。

Bis-propargyl-PEG4

Bis-propargyl-PEG4 Chemical Structure

CAS No. : 159428-42-9

规格 价格 是否有货 数量
50 mg ¥600 In-stock
100 mg ¥900 In-stock
250 mg ¥1800 In-stock
500 mg   询价  
1 g   询价  

* Please select Quantity before adding items.

生物活性

Bis-propargyl-PEG4 is a PEG-based PROTAC linker used in the synthesis of PROTACs. Bis-propargyl-PEG4 is used for the synthesis of demethylvancomycin dimers[1][2].

体外研究
(In Vitro)

Bis-propargyl-PEG4 can be used in the synthesis of demethylvancomycin dimers against vancomycin-resistant enterococcus faecalis[2].

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

分子量

270.32

Formula

C14H22O5

CAS 号

159428-42-9

运输条件

Room temperature in continental US; may vary elsewhere.

储存方式
Pure form -20°C 3 years
4°C 2 years
In solvent -80°C 6 months
-20°C 1 month
参考文献
  • [1]. Pearlie BURNETTE, et al. Dimeric immuno-modulatory compounds against cereblon-based mechanisms. WO2020014489A2.

    [2]. Jiang, et al. Design, synthesis and biological activity of novel demethylvancomycin dimers against vancomycin-resistant enterococcus faecalis. Tetrahedron, 2018: 74(27), 3527–3533.

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

Bis-PEG2-PFP ester

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。

Bis-PEG2-PFP ester 

NH2-PEG3-BOC 是一种不可降解 (non-cleavable) 的含 2 个单元 PEG 的 ADC linker,可用于合成抗体偶联药物 (ADC)。Bis-PEG2-PFP ester 也是一种 PROTAC linker,属于 PEG 类。可用于合成 PROTAC 分子。

Bis-PEG2-PFP ester

Bis-PEG2-PFP ester Chemical Structure

CAS No. : 1314378-18-1

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

Bis-PEG2-PFP ester is also a non-cleavable 2 unit PEG ADC linker used in the synthesis of antibody-drug conjugates (ADCs)[1]. Bis-PEG2-PFP ester is also a PEG-based PROTAC linker that can be used in the synthesis of PROTACs[2].

IC50 & Target

PEGs

 

Alkyl/ether

 

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].
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[2].

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

分子量

538.29

Formula

C20H12F10O6

CAS 号

1314378-18-1

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 David DOROSKI, et al. Cytotoxic peptides and antibody drug conjugates thereof. WO2013072813A2.

    [2]. 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

Bis-PEG3-PFP ester

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。

Bis-PEG3-PFP ester 

Bis-PEG3-PFP ester 是一种 PROTAC linker,属于 PEG 类。可用于合成 PROTAC 分子。

Bis-PEG3-PFP ester

Bis-PEG3-PFP ester Chemical Structure

CAS No. : 1314378-13-6

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

Bis-PEG3-PFP ester is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs[1].

IC50 & Target

PEGs

 

Alkyl/ether

 

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

582.34

Formula

C22H16F10O7

CAS 号

1314378-13-6

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

Bis-PEG4-PFP ester

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。

Bis-PEG4-PFP ester 

Bis-PEG4-PFP ester 是一种 PROTAC linker,属于 PEG 类。可用于合成 PROTAC 分子。

Bis-PEG4-PFP ester

Bis-PEG4-PFP ester Chemical Structure

CAS No. : 1314378-12-5

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

Bis-PEG4-PFP ester is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs[1].

IC50 & Target

PEGs

 

Alkyl/ether

 

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

626.39

Formula

C24H20F10O8

CAS 号

1314378-12-5

运输条件

Room temperature in continental US; may vary elsewhere.

储存方式
Pure form -20°C 3 years
4°C 2 years
In solvent -80°C 6 months
-20°C 1 month
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