1005775-56-3
中文名称
化合物 T13099
英文名称
TC ASK 10
CAS
1005775-56-3
分子式
C21H21N5O.2HCl
更新日期
2025/04/13 11:59:27
分子量
395.89
MOL 文件
1005775-56-3.mol
1005775-56-3 结构式
基本信息
中文别名
化合物 T13099化合物TC ASK 10
英文别名
TC ASK 10ASK1 Inhibitor 10
4-tert-butyl-N-(6-imidazol-1-ylimidazo[1,2-a]pyridin-2-yl)benzamide:hydrochloride
4-(1,1-Dimethylethyl)-N-[6-(1H-imidazol-1-yl)imidazo[1,2-a]pyridin-2-yl]benzamide dihydrochloride
Apoptosis,ASK1,oral,MAP3K,bioavailability,TC ASK-10,TC ASK10,Inhibitor,pharmacokinetic,JNK,TC ASK 10,p38,inhibit,selective,MAP kinase kinase kinase, MEKK, MAPKKK,Phosphorylation
化合物 T13099价格(试剂级)
| 报价日期 | 产品编号 | 产品名称 | CAS号 | 包装 | 价格 |
| 2025/02/08 | HY-103258 | 化合物 T13099 TC ASK 10 | 1005775-56-3 | 1 mg | 371元 |
| 2025/02/08 | HY-103258 | 化合物 T13099 TC ASK 10 | 1005775-56-3 | 10mM * 1mLin DMSO | 824元 |
| 2025/02/08 | HY-103258 | 化合物 T13099 TC ASK 10 | 1005775-56-3 | 5mg | 866元 |
常见问题列表
生物活性
TC ASK 10 (Compound 10) 是一种有效的，选择性的，口服活性的细胞凋亡信号调节激酶 1 (ASK1) 抑制剂，IC50 为 14 nM。TC ASK 10 对其他代表性激酶的抑制活性低于 50％，ASK2 除外 (IC50 为 0.51 μM)。靶点
|
ASK1 14 nM (IC 50 ) |
体外研究
TC ASK 10 (Compound 10; 0-10 μM; 1 hour; INS-1 cells) treatment inhibits streptozotocin (STZ)-induced JNK in INS-1 pancreatic β cells from 0.3 μM. Phosphorylation of p38 is also inhibited in a dosedependent manner.
Western Blot Analysis
| Cell Line: | INS-1 cells |
| Concentration: | 0 μM, 0.3 μM, 1 μM, 3 μM, 10 μM |
| Incubation Time: | 1 hour |
| Result: | Was found to inhibit streptozotocin (STZ)-induced JNK in INS-1 pancreatic β cells from 0.3 μM. Phosphorylation of p38 was also inhibited in a dosedependent manner. |
体内研究
Pharmacokinetic profiles in rats are tested. TC ASK 10 (Compound 10•HCl; rat cassette doing at 0.1 mg/kg, iv and 1 mg/kg, po.) has a good oral bioavailability. The C max , T max and AUC po,0-8h are 285.1 ng/mL, 1.67 h and 275.4 ng.h/mL, respectively for TC ASK 10.