中文名 | GSK717 |
英文名 | GSK717 |
别名 | N-(2-(1-(2-((2,3-二氢-1H-茚-5-基)氨基)-2-氧代乙基)-1H-苯并[D]咪唑-2-基)乙基)-N-甲基苯甲酰胺 |
英文别名 | GSK717 1H-Benzimidazole-1-acetamide, 2-[2-(benzoylmethylamino)ethyl]-N-(2,3-dihydro-1H-inden-5-yl)- N-(2-(1-(2-((2,3-Dihydro-1H-inden-5-yl)amino)-2-oxoethyl)-1H-benzo[d]imidazol-2-yl)ethyl)-N-methylbenzamide |
CAS | 1595278-21-9 |
化学式 | C28H28N4O2 |
分子量 | 452.56 |
密度 | 1.23±0.1 g/cm3(Predicted) |
沸点 | 731.6±60.0 °C(Predicted) |
溶解度 | DMSO : 100 mg/mL |
酸度系数 | 14.05±0.20(Predicted) |
存储条件 | -20℃ |
体外研究 | GSK717 blocks synergy between NOD2 and TLR2. GSK717 does not affect NOD1, TNFR1 and TLR2-mediated responses. GSK717 (5 μM) inhibits the release of IL-8, IL-6, TNFα and IL-1β in primary human monocytes stimulated with MDP. |
参考资料 展开查看 | 1. Rickard DJ, et al. Identification of benzimidazole diamides as selective inhibitors of the nucleotide-binding oligomerization domain 2 (NOD2) signaling pathway. PLoS One. 2013;8(8):e69619. Published 2013 Aug 1. |
1mg | 5mg | 10mg | |
---|---|---|---|
1 mM | 2.21 ml | 11.049 ml | 22.097 ml |
5 mM | 0.442 ml | 2.21 ml | 4.419 ml |
10 mM | 0.221 ml | 1.105 ml | 2.21 ml |
5 mM | 0.044 ml | 0.221 ml | 0.442 ml |
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