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描述 | GSK2795039 acts as an inhibitor of NADPH oxidase 2 (NOX2), showing potency with a mean pIC50 of 6 across various cell-free assays. It effectively reduces the production of reactive oxygen species (ROS) and consumption of NADPH[1]. |
体内研究 | When administered through intraperitoneal injection at 100 mg/kg, 1 hour prior to experimentation, it attenuates activity in a mouse model of acute pancreatitis by diminishing serum amylase levels, which are elevated by systemic cerulein injection[1]. |
体外研究 | A treatment regimen involving GSK2795039 at a concentration of 25 μM for 24 hours decreases the apoptotic levels induced by a combination of FeSO4 and LPS, and also lowers the number of caspase-3-positive PC12 cells[2]. |
Dose | Rat: 3 mg/kg[1] (p.o.); 1 mg/kg[1] (i.v.) Mice: 5 mg/kg, 100 mg/kg[1] (p.o.); 100 mg/kg[1] (i.p.); 1 mg/kg[1] (i.v.) | ||||||||||||||||||||||||||||||
Administration | p.o., i.v., i.p. | ||||||||||||||||||||||||||||||
Pharmacokinetics |
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计算器 | ||||
存储液制备 | 1mg | 5mg | 10mg | |
1 mM 5 mM 10 mM |
2.22mL 0.44mL 0.22mL |
11.10mL 2.22mL 1.11mL |
22.19mL 4.44mL 2.22mL |
CAS号 | 1415925-18-6 |
分子式 | C23H26N6O2S |
分子量 | 450.557 |
别名 | |
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: 105 mg/mL(233.05 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 |