Powder: -20°C for 3 years | In solvent: -80°C for 1 year
GW-311616 hydrochloride is a long duration, orally bioavailable, and selective human neutrophil elastase (HNE) inhibitor (IC50: 22 nM; Ki: 0.31 nM).
规格 | 价格/CNY | 货期 | 数量 | |
---|---|---|---|---|
1 mg | ¥ 1,410 | 35日内发货 | ||
5 mg | ¥ 4,160 | 35日内发货 | ||
10 mg | ¥ 6,930 | 35日内发货 |
产品描述 | GW-311616 hydrochloride is a long duration, orally bioavailable, and selective human neutrophil elastase (HNE) inhibitor (IC50: 22 nM; Ki: 0.31 nM). |
靶点活性 | HNE:(ki)0.31 nM , HNE:22 nM |
体外活性 | GW311616A (20-320 μM; 48 hours; U937 cells) treatment inhibits proliferation and induces apoptosis in leukemia cells. GW-311616 (150 μM; U937 cells) treatment can increase the protein expression levels of Bax and decrease the expression of Bcl-2.GW-311616 (150 μM; 48 hours) markedly suppresses NE activity in U937 and K562 cells lines. |
体内活性 | GW-311616 has moderate terminal elimination half-life (t1/2) of 1.1 hours and 1.5 hours for dog (2 mg/kg, oral), rat (2 mg/kg, oral), respectively.GW-311616 (2 mg/kg;?oral administration) rapidly abolishes the circulation of neutrophil elastase (NE) in dogs, while >90% inhibition is maintained for 4 days.?This prolonged effect is independent to be due to penetration of neutrophils in bone marrow by orally administrated GW-311616. |
别名 | GW311616A |
分子量 | 433.99 |
分子式 | C19H32ClN3O4S |
CAS No. | 197890-44-1 |
Powder: -20°C for 3 years | In solvent: -80°C for 1 year
H2O: 100 mg/mL (230.42 mM)
可选溶剂 | 浓度 体积 质量 | 1 mg | 5 mg | 10 mg | 25 mg |
H2O | 1 mM | 2.3042 mL | 11.521 mL | 23.042 mL | 57.605 mL |
5 mM | 0.4608 mL | 2.3042 mL | 4.6084 mL | 11.521 mL | |
10 mM | 0.2304 mL | 1.1521 mL | 2.3042 mL | 5.7605 mL | |
20 mM | 0.1152 mL | 0.5761 mL | 1.1521 mL | 2.8803 mL | |
50 mM | 0.0461 mL | 0.2304 mL | 0.4608 mL | 1.1521 mL | |
100 mM | 0.023 mL | 0.1152 mL | 0.2304 mL | 0.5761 mL |
对于不同动物的给药剂量换算,您也可以参考 更多...
请在以下方框中输入您的动物实验信息后点击计算,可以得到母液配置方法和体内配方的制备方法: 比如您的给药剂量是10 mg/kg,每只动物体重20 g,给药体积100 μL,一共给药动物10 只,您使用的配方为5% DMSO+30% PEG300+5% Tween 80+60% ddH2O。那么您的工作液浓度为2 mg/mL。
母液配置方法:2 mg 药物溶于 50 μL DMSO (母液浓度为 40 mg/mL), 如您需要配置的浓度超过该产品的溶解度,请先与我们联系。
体内配方的制备方法:取 50 μL DMSO 主液,加入 300 μL PEG300, 混匀澄清,再加 50 μL Tween 80,混匀澄清,再加 600 μL ddH2O, 混匀澄清。
您可能有的问题的答案可以在抑制剂处理说明中找到,包括如何准备库存溶液,如何存储产品,以及基于细胞的分析和动物实验需要特别注意的问题。
GW311616 hydrochloride 197890-44-1 Others GW311616A GW-311616 Hydrochloride GW 311616 Hydrochloride GW311616 Hydrochloride GW-311616 hydrochloride Inhibitor inhibitor inhibit