NQ301
NQ301 性质
熔点 | 241-243 °C(Solv: ethanol (64-17-5)) |
---|---|
沸点 | 476.8±45.0 °C(Predicted) |
密度 | 1.40±0.1 g/cm3(Predicted) |
储存条件 | 2-8°C |
溶解度 | DMSO:10.0(最大浓度 mg/mL);30.7(最大浓度 mM) |
酸度系数(pKa) | -5.25±0.20(Predicted) |
形态 | 粉末 |
颜色 | 淡红色至深红色 |
NQ301 用途与合成方法
Target | Value |
TXA2 receptor
() | |
CD45
(Cell-free assay) | 200 nM |
NQ301 concentration-dependently inhibits collagen (10 mg/mL)-, U46619 (1 mg/mL)- and arachidonic acid (100 mg/mL)-challenged rabbit platelet aggregation, with IC 50 values of 0.60±0.02, 0.58±0.04 and 0.78±0.04 μM, respectively. NQ301 potently suppresses thromboxane B 2 formation by platelets that are exposed to arachidonic acid in a concentration-dependent manner, but had no effect on the production of prostaglandin D 2 , indicating an inhibitory effect on thromboxane A 2 synthase. NQ301 has a potential to inhibit thromboxane A 2 synthase activity with thromboxane A 2 /prostaglandin H 2 receptor blockade, and modulate arachidonic acid liberation as well as 12-hydroxy-5,8,10,14-eicosatetraenoic acid formation in platelets. NQ301 inhibits platelet aggregation by suppression of the intracellular pathway, rather than by direct inhibition of fibrinogen-GPIIb/IIIa complex binding. NQ301 significantly inhibits the increase of cytosolic Ca 2+ concentration and ATP secretion, and also significantly increases platelet cAMP levels in the activated platelets. The antiplatelet activity of NQ301 may be mediated by inhibition of cytosolic Ca 2+ mobilization, enhancement of cAMP production and inhibition of ATP secretion in activated platelets.
NQ301 价格(试剂级)
更新日期 | 产品编号 | 产品名称 | CAS号 | 包装 | 价格 |
---|---|---|---|---|---|
2024-11-08 | HY-101054 | NQ301 | 130089-98-4 | 5mg | 600 |
2024-11-08 | HY-101054 | NQ301 | 130089-98-4 | 10mM * 1mLin DMSO | 660 |