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描述 | (±)-CPSI-1306 is an orally active MIF antagonist[1]. |
Animal study | Treatment with CPSI-1306 leads to a significant decrease in blood glucose levels in mice, which is associated with a reduction in serum levels of inflammatory cytokines[1].CPSI-1306-induced keratinocyte apoptosis can be detected as early as 30 minutes after a single UV irradiation. At 6, 24 and 48 hours after UV irradiation, CPSI-1306-treated mice showed a significant increase in cleaved caspase-3 expression compared to control mice. CPSI-1306 reduces acute UVB-induced keratinocyte DNA damage and UVB-induced acute inflammation[2]. |
计算器 | ||||
存储液制备 | 1mg | 5mg | 10mg | |
1 mM 5 mM 10 mM |
3.22mL 0.64mL 0.32mL |
16.11mL 3.22mL 1.61mL |
32.23mL 6.45mL 3.22mL |
CAS号 | 1309793-47-2 |
分子式 | C15H16F2N2O3 |
分子量 | 310.296 |
别名 | CPSI-1306 |
运输 | 蓝冰 |
存储条件 |
液体 -20°C:3-6个月-80°C:12个月 粉末 Sealed in dry,2-8°C |
溶解度 |
DMSO: 5 mg/mL(16.11 mM),配合低频超声助溶,注意:DMSO长时间开封后,会吸水并导致溶解能力下降,请避免使用长期开封的DMSO |
动物实验配方 |