标签归档：atr

ATR-IN-10

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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。

ATR-IN-10 

ATR-IN-10 是一种有效且高选择性 ATR 激酶的抑制剂，其IC50值为 2.978 μM。

ATR-IN-10

ATR-IN-10 Chemical Structure

CAS No. : 2713577-93-4

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

ATR-IN-10 is a potent and highly selective inhibitor of ataxia telangiectasia mutated and Rad3-Related (ATR) kinase with an IC50 value of 2.978 μM.

IC50 & Target

ATR

2.978 μM (IC50)

分子量

420.51

Formula

C27H24N4O
CAS 号

2713577-93-4
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]. Bin H, et al. Discovery of a potent and highly selective inhibitor of ataxia telangiectasia mutated and Rad3-Related (ATR) kinase: Structural activity relationship and antitumor activity both in vitro and in vivo. Eur J Med Chem. 2022 Feb 12;232:114187.

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

ATR-IN-10

发表于由
回复

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。

ATR-IN-10 

ATR-IN-10 是一种有效且高选择性 ATR 激酶的抑制剂，其IC50值为 2.978 μM。

ATR-IN-10

ATR-IN-10 Chemical Structure

CAS No. : 2713577-93-4

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

ATR-IN-10 is a potent and highly selective inhibitor of ataxia telangiectasia mutated and Rad3-Related (ATR) kinase with an IC50 value of 2.978 μM.

IC50 & Target

ATR

2.978 μM (IC50)

分子量

420.51

Formula

C27H24N4O
CAS 号

2713577-93-4
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]. Bin H, et al. Discovery of a potent and highly selective inhibitor of ataxia telangiectasia mutated and Rad3-Related (ATR) kinase: Structural activity relationship and antitumor activity both in vitro and in vivo. Eur J Med Chem. 2022 Feb 12;232:114187.

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

ATR-IN-10

发表于由
回复

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。

ATR-IN-10 

ATR-IN-10 是一种有效且高选择性 ATR 激酶的抑制剂，其IC50值为 2.978 μM。

ATR-IN-10

ATR-IN-10 Chemical Structure

CAS No. : 2713577-93-4

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

ATR-IN-10 is a potent and highly selective inhibitor of ataxia telangiectasia mutated and Rad3-Related (ATR) kinase with an IC50 value of 2.978 μM.

IC50 & Target

ATR

2.978 μM (IC50)

分子量

420.51

Formula

C27H24N4O
CAS 号

2713577-93-4
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]. Bin H, et al. Discovery of a potent and highly selective inhibitor of ataxia telangiectasia mutated and Rad3-Related (ATR) kinase: Structural activity relationship and antitumor activity both in vitro and in vivo. Eur J Med Chem. 2022 Feb 12;232:114187.

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

ATR-IN-5

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。

ATR-IN-5 

ATR-IN-5 是一种有效的 ATR 抑制剂。ATR 是一类参与基因组稳定性和 DNA 损伤修复的蛋白激酶，是 PIKK 家族的成员。ATR-IN-5具有研究ATR激酶介导的疾病如增殖性疾病和癌症的潜力 (信息摘自专利CN112047938A，化合物D24)。

ATR-IN-5

ATR-IN-5 Chemical Structure

CAS No. : 2601571-19-9

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

ATR-IN-5 is a potent inhibitor of ATR. ATR is a class of protein kinases involved in genome stability and DNA damage repair, and is a member of the PIKK family. ATR-IN-5 has the potential for the research of ATR kinase-mediated diseases such as proliferative diseases and cancer (extracted from patent CN112047938A, compound D24)[1].

分子量

555.60

Formula

C27H32F3N9O
CAS 号

2601571-19-9
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.
参考文献

  • [1]. Zhao, Yanping, et al. 2,4,6-Trisubstituted pyrimidine compounds as atr kinase inhibitors. Patent CN112047938A.

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

ATR-IN-6

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。

ATR-IN-6 

ATR-IN-6 是一种有效的 ATR 抑制剂。ATR 是一类参与基因组稳定性和 DNA 损伤修复的蛋白激酶，是 PIKK 家族的成员。ATR-IN-6 具有研究ATR激酶介导的疾病如增殖性疾病和癌症的潜力 (信息摘自专利 WO2021233376A1，化合物 A22)。

ATR-IN-6

ATR-IN-6 Chemical Structure

CAS No. : 2746446-99-9

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

ATR-IN-6 is a potent inhibitor of ATR. ATR is a class of protein kinases involved in genome stability and DNA damage repair, and is a member of the PIKK family. ATR-IN-6 has the potential for the research of ATR kinase-mediated diseases such as proliferative diseases and cancer (extracted from patent WO2021233376A1, compound A22)[1].

分子量

513.57

Formula

C28H28FN7O2
CAS 号

2746446-99-9
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.
参考文献

  • [1]. Zhao, Yanping, et al. 2,4,6-Trisubstituted pyrimidine compounds as atr kinase inhibitors. Patent WO2021233376A1.

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

ATR-IN-5

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。

ATR-IN-5 

ATR-IN-5 是一种有效的 ATR 抑制剂。ATR 是一类参与基因组稳定性和 DNA 损伤修复的蛋白激酶，是 PIKK 家族的成员。ATR-IN-5具有研究ATR激酶介导的疾病如增殖性疾病和癌症的潜力 (信息摘自专利CN112047938A，化合物D24)。

ATR-IN-5

ATR-IN-5 Chemical Structure

CAS No. : 2601571-19-9

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

ATR-IN-5 is a potent inhibitor of ATR. ATR is a class of protein kinases involved in genome stability and DNA damage repair, and is a member of the PIKK family. ATR-IN-5 has the potential for the research of ATR kinase-mediated diseases such as proliferative diseases and cancer (extracted from patent CN112047938A, compound D24)[1].

分子量

555.60

Formula

C27H32F3N9O
CAS 号

2601571-19-9
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.
参考文献

  • [1]. Zhao, Yanping, et al. 2,4,6-Trisubstituted pyrimidine compounds as atr kinase inhibitors. Patent CN112047938A.

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

ATR-IN-5

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。

ATR-IN-5 

ATR-IN-5 是一种有效的 ATR 抑制剂。ATR 是一类参与基因组稳定性和 DNA 损伤修复的蛋白激酶，是 PIKK 家族的成员。ATR-IN-5具有研究ATR激酶介导的疾病如增殖性疾病和癌症的潜力 (信息摘自专利CN112047938A，化合物D24)。

ATR-IN-5

ATR-IN-5 Chemical Structure

CAS No. : 2601571-19-9

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

ATR-IN-5 is a potent inhibitor of ATR. ATR is a class of protein kinases involved in genome stability and DNA damage repair, and is a member of the PIKK family. ATR-IN-5 has the potential for the research of ATR kinase-mediated diseases such as proliferative diseases and cancer (extracted from patent CN112047938A, compound D24)[1].

分子量

555.60

Formula

C27H32F3N9O
CAS 号

2601571-19-9
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.
参考文献

  • [1]. Zhao, Yanping, et al. 2,4,6-Trisubstituted pyrimidine compounds as atr kinase inhibitors. Patent CN112047938A.

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

ATR-IN-6

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。

ATR-IN-6 

ATR-IN-6 是一种有效的 ATR 抑制剂。ATR 是一类参与基因组稳定性和 DNA 损伤修复的蛋白激酶，是 PIKK 家族的成员。ATR-IN-6 具有研究ATR激酶介导的疾病如增殖性疾病和癌症的潜力 (信息摘自专利 WO2021233376A1，化合物 A22)。

ATR-IN-6

ATR-IN-6 Chemical Structure

CAS No. : 2746446-99-9

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

ATR-IN-6 is a potent inhibitor of ATR. ATR is a class of protein kinases involved in genome stability and DNA damage repair, and is a member of the PIKK family. ATR-IN-6 has the potential for the research of ATR kinase-mediated diseases such as proliferative diseases and cancer (extracted from patent WO2021233376A1, compound A22)[1].

分子量

513.57

Formula

C28H28FN7O2
CAS 号

2746446-99-9
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.
参考文献

  • [1]. Zhao, Yanping, et al. 2,4,6-Trisubstituted pyrimidine compounds as atr kinase inhibitors. Patent WO2021233376A1.

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

ATR-IN-7

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。

ATR-IN-7 

ATR-IN-7 是一种有效的 ATR 抑制剂。ATR 是一类参与基因组稳定性和 DNA 损伤修复的蛋白激酶，是 PIKK 家族的成员。ATR-IN-7 具有研究ATR激酶介导的疾病如增殖性疾病和癌症的潜力 (信息摘自专利 WO2021238999A1，化合物 1)。

ATR-IN-7

ATR-IN-7 Chemical Structure

CAS No. : 2741917-74-6

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

ATR-IN-7 is a potent inhibitor of ATR. ATR is a class of protein kinases involved in genome stability and DNA damage repair, and is a member of the PIKK family. ATR-IN-7 has the potential for the research of ATR kinase-mediated diseases such as proliferative diseases and cancer (extracted from patent WO2021238999A1, compound 1)[1].

分子量

407.44

Formula

C21H22FN7O
CAS 号

2741917-74-6
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]. Kun Fang, et al. Fluorinated pyrrolopyridines and their applications. Patent WO2021238999A1.

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

ATR-IN-6

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。

ATR-IN-6 

ATR-IN-6 是一种有效的 ATR 抑制剂。ATR 是一类参与基因组稳定性和 DNA 损伤修复的蛋白激酶，是 PIKK 家族的成员。ATR-IN-6 具有研究ATR激酶介导的疾病如增殖性疾病和癌症的潜力 (信息摘自专利 WO2021233376A1，化合物 A22)。

ATR-IN-6

ATR-IN-6 Chemical Structure

CAS No. : 2746446-99-9

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

ATR-IN-6 is a potent inhibitor of ATR. ATR is a class of protein kinases involved in genome stability and DNA damage repair, and is a member of the PIKK family. ATR-IN-6 has the potential for the research of ATR kinase-mediated diseases such as proliferative diseases and cancer (extracted from patent WO2021233376A1, compound A22)[1].

分子量

513.57

Formula

C28H28FN7O2
CAS 号

2746446-99-9
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.
参考文献

  • [1]. Zhao, Yanping, et al. 2,4,6-Trisubstituted pyrimidine compounds as atr kinase inhibitors. Patent WO2021233376A1.

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

ATR-IN-7

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。

ATR-IN-7 

ATR-IN-7 是一种有效的 ATR 抑制剂。ATR 是一类参与基因组稳定性和 DNA 损伤修复的蛋白激酶，是 PIKK 家族的成员。ATR-IN-7 具有研究ATR激酶介导的疾病如增殖性疾病和癌症的潜力 (信息摘自专利 WO2021238999A1，化合物 1)。

ATR-IN-7

ATR-IN-7 Chemical Structure

CAS No. : 2741917-74-6

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

ATR-IN-7 is a potent inhibitor of ATR. ATR is a class of protein kinases involved in genome stability and DNA damage repair, and is a member of the PIKK family. ATR-IN-7 has the potential for the research of ATR kinase-mediated diseases such as proliferative diseases and cancer (extracted from patent WO2021238999A1, compound 1)[1].

分子量

407.44

Formula

C21H22FN7O
CAS 号

2741917-74-6
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]. Kun Fang, et al. Fluorinated pyrrolopyridines and their applications. Patent WO2021238999A1.

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

ATR-IN-12

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。

ATR-IN-12 

ATR-IN-12 (Compound 5g) 是一种有效的共济失调毛细血管扩张和 Rad3 相关 (ATR) 激酶抑制剂，IC50 值 0.007 μM。ATR-IN-12 显示出良好的抗肿瘤活性并显着降低 ATR 及其下游信号蛋白的磷酸化水平。ATR-IN-12 是一种很有前途的先导化合物，可用于后续针对 ATR 激酶的药物发现。

ATR-IN-12

ATR-IN-12 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

ATR-IN-12 (Compound 5g) is a potent inhibitor of ataxia telangiectasia and Rad3-related (ATR) kinase with an IC50 value of 0.007 μM. ATR-IN-12 displays good anti-tumor activity and significantly reduces the phosphorylation level of ATR and its downstream signaling protein. ATR-IN-12 is a promising lead compound for subsequent drug discovery targeting ATR kinase[1].

分子量

441.55

Formula

C22H27N5O3S
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]. Chen P, et al. Discovery of 6,7-dihydro-5H-pyrrolo[3,4-d] pyrimidine derivatives as a new class of ATR inhibitors. Bioorg Med Chem Lett. 2022;63:128651.

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

ATR-IN-12

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。

ATR-IN-12 

ATR-IN-12 (Compound 5g) 是一种有效的共济失调毛细血管扩张和 Rad3 相关 (ATR) 激酶抑制剂，IC50 值 0.007 μM。ATR-IN-12 显示出良好的抗肿瘤活性并显着降低 ATR 及其下游信号蛋白的磷酸化水平。ATR-IN-12 是一种很有前途的先导化合物，可用于后续针对 ATR 激酶的药物发现。

ATR-IN-12

ATR-IN-12 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

ATR-IN-12 (Compound 5g) is a potent inhibitor of ataxia telangiectasia and Rad3-related (ATR) kinase with an IC50 value of 0.007 μM. ATR-IN-12 displays good anti-tumor activity and significantly reduces the phosphorylation level of ATR and its downstream signaling protein. ATR-IN-12 is a promising lead compound for subsequent drug discovery targeting ATR kinase[1].

分子量

441.55

Formula

C22H27N5O3S
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]. Chen P, et al. Discovery of 6,7-dihydro-5H-pyrrolo[3,4-d] pyrimidine derivatives as a new class of ATR inhibitors. Bioorg Med Chem Lett. 2022;63:128651.

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

ATR-IN-12

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。

ATR-IN-12 

ATR-IN-12 (Compound 5g) 是一种有效的共济失调毛细血管扩张和 Rad3 相关 (ATR) 激酶抑制剂，IC50 值 0.007 μM。ATR-IN-12 显示出良好的抗肿瘤活性并显着降低 ATR 及其下游信号蛋白的磷酸化水平。ATR-IN-12 是一种很有前途的先导化合物，可用于后续针对 ATR 激酶的药物发现。

ATR-IN-12

ATR-IN-12 Chemical Structure

规格 是否有货
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生物活性

ATR-IN-12 (Compound 5g) is a potent inhibitor of ataxia telangiectasia and Rad3-related (ATR) kinase with an IC50 value of 0.007 μM. ATR-IN-12 displays good anti-tumor activity and significantly reduces the phosphorylation level of ATR and its downstream signaling protein. ATR-IN-12 is a promising lead compound for subsequent drug discovery targeting ATR kinase[1].

分子量

441.55

Formula

C22H27N5O3S
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]. Chen P, et al. Discovery of 6,7-dihydro-5H-pyrrolo[3,4-d] pyrimidine derivatives as a new class of ATR inhibitors. Bioorg Med Chem Lett. 2022;63:128651.

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ATR-IN-11

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。

ATR-IN-11 

ATR-IN-11 (Compound Hit01) 是共济失调毛细血管扩张症和 Rad3 相关 (ATR) 激酶的有效抑制剂。ATR 激酶是 DNA 损伤反应 (DDR) 中的关键调节蛋白，负责感知复制压力 (RS)。ATR-IN-11 是一种有前途的先导化合物，可用于后续针对 ATR 激酶的药物发现。 ATR-IN-11具有研究癌症疾病的潜力。

ATR-IN-11

ATR-IN-11 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

ATR-IN-11 (Compound Hit01) is a potent inhibitor of ataxia telangiectasia and Rad3-related (ATR) kinase. ATR kinase is a key regulating protein within the DNA damage response (DDR), responsible for sensing replication stress (RS). ATR-IN-11 is a promising lead compound for subsequent drug discovery targeting ATR kinase. ATR-IN-11 has the potential for the research of cancer disease[1].

分子量

446.54

Formula

C25H30N6O2
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]. Chen P, et al. Discovery of 6,7-dihydro-5H-pyrrolo[3,4-d] pyrimidine derivatives as a new class of ATR inhibitors. Bioorg Med Chem Lett. 2022;63:128651.

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

ATR-IN-11

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。

ATR-IN-11 

ATR-IN-11 (Compound Hit01) 是共济失调毛细血管扩张症和 Rad3 相关 (ATR) 激酶的有效抑制剂。ATR 激酶是 DNA 损伤反应 (DDR) 中的关键调节蛋白，负责感知复制压力 (RS)。ATR-IN-11 是一种有前途的先导化合物，可用于后续针对 ATR 激酶的药物发现。 ATR-IN-11具有研究癌症疾病的潜力。

ATR-IN-11

ATR-IN-11 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

ATR-IN-11 (Compound Hit01) is a potent inhibitor of ataxia telangiectasia and Rad3-related (ATR) kinase. ATR kinase is a key regulating protein within the DNA damage response (DDR), responsible for sensing replication stress (RS). ATR-IN-11 is a promising lead compound for subsequent drug discovery targeting ATR kinase. ATR-IN-11 has the potential for the research of cancer disease[1].

分子量

446.54

Formula

C25H30N6O2
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]. Chen P, et al. Discovery of 6,7-dihydro-5H-pyrrolo[3,4-d] pyrimidine derivatives as a new class of ATR inhibitors. Bioorg Med Chem Lett. 2022;63:128651.

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

ATR-IN-11

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。

ATR-IN-11 

ATR-IN-11 (Compound Hit01) 是共济失调毛细血管扩张症和 Rad3 相关 (ATR) 激酶的有效抑制剂。ATR 激酶是 DNA 损伤反应 (DDR) 中的关键调节蛋白，负责感知复制压力 (RS)。ATR-IN-11 是一种有前途的先导化合物，可用于后续针对 ATR 激酶的药物发现。 ATR-IN-11具有研究癌症疾病的潜力。

ATR-IN-11

ATR-IN-11 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

ATR-IN-11 (Compound Hit01) is a potent inhibitor of ataxia telangiectasia and Rad3-related (ATR) kinase. ATR kinase is a key regulating protein within the DNA damage response (DDR), responsible for sensing replication stress (RS). ATR-IN-11 is a promising lead compound for subsequent drug discovery targeting ATR kinase. ATR-IN-11 has the potential for the research of cancer disease[1].

分子量

446.54

Formula

C25H30N6O2
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]. Chen P, et al. Discovery of 6,7-dihydro-5H-pyrrolo[3,4-d] pyrimidine derivatives as a new class of ATR inhibitors. Bioorg Med Chem Lett. 2022;63:128651.

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

ATR-IN-8

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。

ATR-IN-8 

ATR-IN-8 是一种有效的 ATR 抑制剂。ATR是同源重组修复途径中的关键酶，属于 PIKK 家族。ATR-IN-8具有研究癌症疾病的潜力 (摘自专利 WO2021143821A1，化合物 3)。

ATR-IN-8

ATR-IN-8 Chemical Structure

CAS No. : 2672511-20-3

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

ATR-IN-8 is a potent inhibitor of ATR. ATR is a key enzyme in the homologous recombination repair pathway and belongs to the PIKK family. ATR-IN-8 has the potential for the research of cancer diseases (extracted from patent WO2021143821A1, compound 3)[1].

分子量

410.49

Formula

C20H22N6O2S
CAS 号

2672511-20-3
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]. Li Xin, et al. Thickened heteroaryl derivatives, their preparation methods and their application in medicine. Patent WO2021143821A1.

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

ATR-IN-8

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。

ATR-IN-8 

ATR-IN-8 是一种有效的 ATR 抑制剂。ATR是同源重组修复途径中的关键酶，属于 PIKK 家族。ATR-IN-8具有研究癌症疾病的潜力 (摘自专利 WO2021143821A1，化合物 3)。

ATR-IN-8

ATR-IN-8 Chemical Structure

CAS No. : 2672511-20-3

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

ATR-IN-8 is a potent inhibitor of ATR. ATR is a key enzyme in the homologous recombination repair pathway and belongs to the PIKK family. ATR-IN-8 has the potential for the research of cancer diseases (extracted from patent WO2021143821A1, compound 3)[1].

分子量

410.49

Formula

C20H22N6O2S
CAS 号

2672511-20-3
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]. Li Xin, et al. Thickened heteroaryl derivatives, their preparation methods and their application in medicine. Patent WO2021143821A1.

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

ATR-IN-8

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。

ATR-IN-8 

ATR-IN-8 是一种有效的 ATR 抑制剂。ATR是同源重组修复途径中的关键酶，属于 PIKK 家族。ATR-IN-8具有研究癌症疾病的潜力 (摘自专利 WO2021143821A1，化合物 3)。

ATR-IN-8

ATR-IN-8 Chemical Structure

CAS No. : 2672511-20-3

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

ATR-IN-8 is a potent inhibitor of ATR. ATR is a key enzyme in the homologous recombination repair pathway and belongs to the PIKK family. ATR-IN-8 has the potential for the research of cancer diseases (extracted from patent WO2021143821A1, compound 3)[1].

分子量

410.49

Formula

C20H22N6O2S
CAS 号

2672511-20-3
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]. Li Xin, et al. Thickened heteroaryl derivatives, their preparation methods and their application in medicine. Patent WO2021143821A1.

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