中文名 | BX 430 |
英文名 | BX 430 |
别名 | 化合物BX430 1-(2,6-二溴-4-异丙基苯基)-3-(吡啶-3-基)脲 |
英文别名 | BX 430 1-(2,6-Dibromo-4-isopropylphenyl)-3-(pyridin-3-yl)urea N-[2,6-Dibromo-4-(1-methylethyl)phenyl]-N'-(3-pyridinyl)urea Urea, N-[2,6-dibromo-4-(1-methylethyl)phenyl]-N'-3-pyridinyl- |
CAS | 688309-70-8 |
化学式 | C15H15Br2N3O |
分子量 | 413.11 |
熔点 | 164-168°C |
溶解度 | DMSO (微溶) 、甲醇 (微溶) |
存储条件 | 2-8°C |
外观 | 固体 |
颜色 | White |
靶点 | human P2X4 receptor channels |
体外研究 | BX430 has virtually no functional impact on all other P2X subtypes, namely, P2X1-P2X3, P2X5, and P2X7, at 10-100 times its IC 50 . BX430 is a potent antagonist of zebrafish P2X4 but has no effect on rat and mouse P2X4 orthologs. Human P2X4-expressing cells treated with thapsigargin plus BX430 shows a significant reduction in the intracellular calcium rise evoked by ATP. BX430 (5 μM) markedly reduces the amplitude of ATP-evoked intracellular calcium responses in THP-1 cells. |
1mg | 5mg | 10mg | |
---|---|---|---|
1 mM | 2.421 ml | 12.103 ml | 24.207 ml |
5 mM | 0.484 ml | 2.421 ml | 4.841 ml |
10 mM | 0.242 ml | 1.21 ml | 2.421 ml |
5 mM | 0.048 ml | 0.242 ml | 0.484 ml |
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