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- 详细信息
- 文献和实验
- 技术资料
- 保存条件：
Powder: -20°C, 3 years; 4°C, 2 years.In solvent: -80°C, 6 months; -20°C, 1 month.
- 库存：
货期：1-2天
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MedChemExpress LLC
- 规格：
10 mM * 1 mL/5 mg/10 mg/25 mg/50 mg/100 mg
| 规格： | 10 mM * 1 mL | 产品价格： | ￥660.0 |
|---|---|---|---|
| 规格： | 5 mg | 产品价格： | ￥600.0 |
| 规格： | 10 mg | 产品价格： | ￥900.0 |
| 规格： | 25 mg | 产品价格： | ￥1500.0 |
| 规格： | 50 mg | 产品价格： | ￥2500.0 |
| 规格： | 100 mg | 产品价格： | ￥4500.0 |
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NQ301
CAS No. : 130089-98-4
MCE 国际站：NQ301
产品活性：NQ301是一种抗血栓剂; 可抑制胶原蛋白激发的兔血小板聚集，IC50值为10 mg/mL。
研究领域：Metabolic Enzyme/Protease
作用靶点：Thrombin
In Vitro: NQ301 concentration-dependently inhibits collagen (10 mg/mL)-, U46619 (1 mg/mL)- and arachidonic acid (100 mg/mL)-challenged rabbit platelet aggregation, with IC50 values of 0.60±0.02, 0.58±0.04 and 0.78±0.04 μM, respectively. NQ301 potently suppresses thromboxane B2 formation by platelets that are exposed to arachidonic acid in a concentration-dependent manner, but had no effect on the production of prostaglandin D2, indicating an inhibitory effect on thromboxane A2 synthase. NQ301 has a potential to inhibit thromboxane A2 synthase activity with thromboxane A2/prostaglandin H2 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 Ca2+ 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 Ca2+ mobilization, enhancement of cAMP production and inhibition of ATP secretion in activated platelets.
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文献和实验9(3):301–309, 2008). Integrin α4 β7 is not an entry receptor for HIV-1, although it can facilitate virion attachment to target cells (Arthos et al., Nat Immunol 9(3):301–309, 2008; Cicala et al., Proc Natl Acad Sci U S A 106:20877–20882, 2009). Recombinant
=1.215(cm). 本例自由度v =n1+n2-2=98,查t界值表[表内自由度一栏无98，可用内插法（从略）或用v =100估计]。T0.05(100)=1.948,t0.01(100)=2.626,今t=2.505＞t0.05(1000,P＜0.05,按α=0.05检验水准拒绝H0，接受H1，可认为广西瑶族和侗族妇女骨盆入口前后径不同，前者大于后者。 四、完全随机设计的两样本几何均数比较 医学上有些资料为等比资料或正态分布资料，宜用几何
由表1可见，采用恒流、恒压和程序升压方式，利用SPME-GC技术分析PAHs所得的保留指数同样相差不大，能保持在1个保留指数单位范围内.图1为利用SMPE-GC方法所得的气相色谱图. 表1 不同分析条件下多环芳烃保留指数的比较 编号 化合物 恒压 溶流恒流 升压 恒压 SPME恒流 升压 1 萘 200.00 200.00 200.00 200.00 200.00 200.00 2 联苯 235.98 236.15 235096 236.07 236.25 236.00
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