CRT0273750
目录号 : GC62215CRT0273750 是 ATX 抑制剂的先导化合物,并调节血浆中 LPA 水平。CRT0273750 可用于 ATX/LPA 依赖性癌症模型。
Cas No.:1979939-16-6
Sample solution is provided at 25 µL, 10mM.
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CRT0273750 is an autotaxin (ATX) inhibitor and modulates LPA levels in plasm (IC50 = 0.014 μM). CRT0273750 can be used in ATX/LPA-dependent models of cancer[1].
CRT0273750 shows high potency in both the biochemical (IC50 = 0.01 μM) and plasma choline release assay(IC50 = 0.014 μM)[1].CRT0273750 is also shown to inhibit the migration of 4T1 cells with an EC50 of 0.025μM[1].
CRT0273750 (1 mg/kg; i.v.)has a moderate blood clearance, with value of 41 mL/min/kg[1].CRT0273750 (10 mg/kg; oral administration) treatment shows the Cmax, AUC and t1/2 values of 3.8 µM, 3.2 µM.h and 1.4 h, respectively[1].CRT0273750 (10, 30 and 100 mg/kg; oral administration) shows a proportional increase[1].
[1]. Shah P, et al. Discovery of potent inhibitors of the lysophospholipase autotaxin. Bioorg Med Chem Lett. 2016;26(22):5403-5410.
Cas No. | 1979939-16-6 | SDF | |
分子式 | C25H22ClF3N4O2 | 分子量 | 502.92 |
溶解度 | DMSO : 250 mg/mL (497.10 mM; Need ultrasonic) | 储存条件 | Store at -20°C |
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1 mg | 5 mg | 10 mg | |
1 mM | 1.9884 mL | 9.9419 mL | 19.8839 mL |
5 mM | 0.3977 mL | 1.9884 mL | 3.9768 mL |
10 mM | 0.1988 mL | 0.9942 mL | 1.9884 mL |
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2.
一定要按照顺序依次将溶剂加入,进行下一步操作之前必须保证上一步操作得到的是澄清的溶液,可采用涡旋、超声或水浴加热等物理方法助溶。
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Discovery of potent inhibitors of the lysophospholipase autotaxin
Bioorg Med Chem Lett 2016 Nov 15;26(22):5403-5410.PMID:27780639DOI:10.1016/j.bmcl.2016.10.036
The autotaxin-lysophosphatidic acid (ATX-LPA) axis has been implicated in several disease conditions including inflammation, fibrosis and cancer. This makes ATX an attractive drug target and its inhibition may lead to useful therapeutic agents. Through a high throughput screen (HTS) we identified a series of small molecule inhibitors of ATX which have subsequently been optimized for potency, selectivity and developability properties. This has delivered drug-like compounds such as 9v (CRT0273750) which modulate LPA levels in plasma and are suitable for in vivo studies. X-ray crystallography has revealed that these compounds have an unexpected binding mode in that they do not interact with the active site zinc ions but instead occupy the hydrophobic LPC pocket extending from the active site of ATX together with occupying the LPA 'exit' channel.