![]() 5-[4-苯基-5-(三氟甲基)-2-噻吩基]-3-[3-(三氟甲基)苯基]-1,2,4-恶二唑结构式
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常用名 | 5-[4-苯基-5-(三氟甲基)-2-噻吩基]-3-[3-(三氟甲基)苯基]-1,2,4-恶二唑 | 英文名 | SEW2871 |
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CAS号 | 256414-75-2 | 分子量 | 440.362 | |
密度 | 1.4±0.1 g/cm3 | 沸点 | 490.3±55.0 °C at 760 mmHg | |
分子式 | C20H10F6N2OS | 熔点 | 94.5-95.3ºC | |
MSDS | 中文版 美版 | 闪点 | 250.3±31.5 °C | |
符号 |
![]() GHS06 |
信号词 | Danger |
用途SEW2871 是高度选择性的,具有口服活性的 S1P1 激动剂,EC50 为 13.8 nM。SEW2871 激活 ERK,Akt 和 Rac 信号通路,并诱导 S1P1 内在化和再循环。SEW2871 减少血液中的淋巴细胞数量,并在糖尿病,阿尔茨海默氏病,肝纤维化和炎症反应方面具有治疗意义。 |
中文名 | 5-[4-苯基-5-(三氟甲基)-2-噻吩]-3-[3-(三氟甲基)苯基]-1,2,4-噁二唑 |
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英文名 | 5-[4-phenyl-5-(trifluoromethyl)thiophen-2-yl]-3-[3-(trifluoromethyl)phenyl]-1,2,4-oxadiazole |
中文别名 | 5-[4-苯基-5-(三氟甲基)-2-噻吩基]-3-[3-(三氟甲基)苯基]-1,2,4-恶二唑 |
英文别名 | 更多 |
描述 | SEW2871 是高度选择性的,具有口服活性的 S1P1 激动剂,EC50 为 13.8 nM。SEW2871 激活 ERK,Akt 和 Rac 信号通路,并诱导 S1P1 内在化和再循环。SEW2871 减少血液中的淋巴细胞数量,并在糖尿病,阿尔茨海默氏病,肝纤维化和炎症反应方面具有治疗意义。 |
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靶点 |
EC50: 13.8 nM (S1P1)[2] |
参考文献 |
密度 | 1.4±0.1 g/cm3 |
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沸点 | 490.3±55.0 °C at 760 mmHg |
熔点 | 94.5-95.3ºC |
分子式 | C20H10F6N2OS |
分子量 | 440.362 |
闪点 | 250.3±31.5 °C |
精确质量 | 440.041809 |
PSA | 67.16000 |
LogP | 8.42 |
外观性状 | 白色固体 |
蒸汽压 | 0.0±1.2 mmHg at 25°C |
折射率 | 1.535 |
储存条件 | 2-8°C,避光干燥密封 |
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1,2,4-Oxadiazole, 5-[4-phenyl-5-(trifluoromethyl)-2-thienyl]-3-[3-(trifluoromethyl)phenyl]- |
5-[4-Phenyl-5-(trifluoromethyl)-2-thienyl]-3-[3-(trifluoromethyl)phenyl]-1,2,4-oxadiazole |
5-[4-phenyl-5-(trifluoromethyl)thiophen-2-yl]-3-[3-(trifluoromethyl)phenyl]-1,2,4-oxadiazole |
5-[4-Phenyl-5-(trifluoromethyl)-2-thienyl]-3-[3-(trifluoromethyl)phenyl]- 1,2,4-oxadiazole |
5-[4-phenyl-5-(trifluoromethyl)thien-2-yl]-3-[3-(trifluoromethyl)phenyl]-1,2,4-oxadiazole |