DDR1-IN-6

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。

DDR1-IN-6 

DDR1-IN-6 是选择性的盘状结构域受体家族成员 1 (DDR1) 抑制剂,IC50 为 9.72 nM。DDR1-IN-6 抑制 DDR1b (Y513) 自磷酸化,IC50 为 9.7 nM。DDR1-IN-6 具有抗癌活性。

DDR1-IN-6

DDR1-IN-6 Chemical Structure

CAS No. : 2416021-47-9

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生物活性

DDR1-IN-6 is a selective Discoidin Domain Receptor family, member 1 (DDR1) inhibitor with an IC50 of 9.72 nM. DDR1-IN-6 inhibits auto-phosphorylation DDR1b (Y513) with an IC50 of 9.7 nM. DDR1-IN-6 has anti-cancer activity[1].

IC50 & Target[1]

DDR1

9.72 nM (IC50)

体外研究
(In Vitro)

DDR1-IN-6 (compound 1; for 24 hours) inhibits collagen production in human hepatic stellate cell LX-2 (IC50=13 nM)[1].
DDR1-IN-6 (72 hours) has cytotoxicity in LX-2 cells (CC50=3 μM)[1].
DDR1-IN-6 (0-30 μM) has anti-proliferation effects on primary tumor cells freshly isolated from PC-07-0024 (IC50=5.7 μM of 3 days; IC50=2.65 μM of 6 days) and LU-01-0523 derived xenograft (PDX) tumor model (IC50>30 μM of 3 days; IC50>30 μM of 6 days)[1].

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

分子量

433.39

Formula

C23H14F3N5O

CAS 号

2416021-47-9

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]. Aleksandr M. Aliper, et al. Kinase inhibitors. WO2020079652A1.

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