LDHA/PDKs-IN-1

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。

LDHA/PDKs-IN-1 

LDHA/PDKs-IN-1 (compound 20e) 是一种有效的 PDKs 和 LDHA 双重抑制剂,IC50s 分别为 0.8 和 0.15 μM。LDHA/PDKs-IN-1 减少 A549 细胞增殖,EC50 为 13.2 μM,减少乳酸形成,增加耗氧量。LDHA/PDKs-IN-1 具有研究癌症疾病的潜力。

LDHA/PDKs-IN-1

LDHA/PDKs-IN-1 Chemical Structure

CAS No. : 2490699-40-4

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

LDHA/PDKs-IN-1 (compound 20e) is a potent and dual inhibitor of PDKs and LDHA with IC50s of 0.8 and 0.15 μM, respectively. LDHA/PDKs-IN-1 reduces A549 cell proliferation with an EC50 of 13.2 μM and decreases the lactate formation, and increases oxygen consumption. LDHA/PDKs-IN-1 has the potential for the research of cancer diseases[1].

分子量

360.38

Formula

C19H21FN2O4

CAS 号

2490699-40-4

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]. Xiang S, et al. Development of dual inhibitors targeting pyruvate dehydrogenase kinases and human lactate dehydrogenase A: High-throughput virtual screening, synthesis and biological validation. Eur J Med Chem. 2020;203:112579.

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

LDHA/PDKs-IN-2

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。

LDHA/PDKs-IN-2 

LDHA/PDKs-IN-2 (compound 20k) 是一种有效的 PDKs 和 LDHA 双重抑制剂,IC50s 分别为 1.6 和 0.7 μM。LDHA/PDKs-IN-2 减少 A549 细胞增殖,EC50 为 15.7 μM,减少乳酸形成,增加耗氧量。LDHA/PDKs-IN-2 具有研究癌症疾病的潜力。

LDHA/PDKs-IN-2

LDHA/PDKs-IN-2 Chemical Structure

CAS No. : 2490699-44-8

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

LDHA/PDKs-IN-2 (compound 20k) is a potent and dual inhibitor of PDKs and LDHA with IC50s of 1.6 and 0.7 μM, respectively. LDHA/PDKs-IN-2 reduces A549 cell proliferation with an EC50 of 15.7 μM and decreases the lactate formation, and increases oxygen consumption. LDHA/PDKs-IN-2 has the potential for the research of cancer diseases[1].

分子量

332.35

Formula

C17H20N2O5

CAS 号

2490699-44-8

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]. Xiang S, et al. Development of dual inhibitors targeting pyruvate dehydrogenase kinases and human lactate dehydrogenase A: High-throughput virtual screening, synthesis and biological validation. Eur J Med Chem. 2020;203:112579.

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