PTUPB结构式
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常用名 | PTUPB | 英文名 | PTUPB |
|---|---|---|---|---|
| CAS号 | 1287761-01-6 | 分子量 | 543.561 | |
| 密度 | 1.4±0.1 g/cm3 | 沸点 | N/A | |
| 分子式 | C26H24F3N5O3S | 熔点 | N/A | |
| MSDS | N/A | 闪点 | N/A |
PTUPB用途PTUPB是一种新型双作用COX-2/sEH抑制剂,IC50为1.26 uM/0.9 nM,不抑制COX-1(IC50>100 uM);减少肾损伤参数,减少ZDF大鼠的炎症和氧化应激标志物;表现出比单独使用相同剂量的COX-2抑制剂(塞来昔布)或sEH抑制剂(t-AUCB)更有效,在体内显示体内抗异常性疼痛活性;还通过靶向EGFR和透明质酸介导的运动受体抑制胶质母细胞瘤生长,增强顺铂的抗肿瘤功效。 |
| 英文名 | 4-{5-Phenyl-3-[3-({[4-(trifluoromethyl)phenyl]carbamoyl}amino)propyl]-1H-pyrazol-1-yl}benzenesulfonamide |
|---|---|
| 英文别名 | 更多 |
| 描述 | PTUPB是一种新型双作用COX-2/sEH抑制剂,IC50为1.26 uM/0.9 nM,不抑制COX-1(IC50>100 uM);减少肾损伤参数,减少ZDF大鼠的炎症和氧化应激标志物;表现出比单独使用相同剂量的COX-2抑制剂(塞来昔布)或sEH抑制剂(t-AUCB)更有效,在体内显示体内抗异常性疼痛活性;还通过靶向EGFR和透明质酸介导的运动受体抑制胶质母细胞瘤生长,增强顺铂的抗肿瘤功效。 |
|---|---|
| 参考文献 | References 1. Hye Khan MA, et al. Prostaglandins Other Lipid Mediat. 2016 Sep;125:40-7. 2. Li J, et al. Oncotarget. 2017 Sep 15;8(50):87353-87363. 3. Wang F, et al. Mol Cancer Ther. 2018 Feb;17(2):474-483. 4. Hwang SH, et al. J Med Chem. 2011 Apr 28;54(8):3037-50. View Related Products by Target Cyclooxygenase (COX) |
| 密度 | 1.4±0.1 g/cm3 |
|---|---|
| 分子式 | C26H24F3N5O3S |
| 分子量 | 543.561 |
| 精确质量 | 543.155212 |
| LogP | 4.91 |
| 折射率 | 1.626 |
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| 4-{5-Phenyl-3-[3-({[4-(trifluoromethyl)phenyl]carbamoyl}amino)propyl]-1H-pyrazol-1-yl}benzenesulfonamide |