溶解性 | 25°C: DMSO |
存贮条件 | 储存温度-20°C |
产品介绍 | Vilanterol (GW642444; GW 642444X)是吸入型长效β2激动剂。 |
生化机理 | in vitro:Vilanterol displayed a subnanomolar affinity for the β(2)-AR that was comparable with that of salmeterol but higher than olodaterol, formoterol, and indacaterol. In cAMP functional activity studies, vilanterol demonstrated similar selectivity as salmeterol for β(2)- over β(1)-AR and β(3)-AR, but a significantly improved selectivity profile than formoterol and indacaterol. Vilanterolalso showed a level of intrinsic efficacy that was comparable to indacaterol but significantly greater than that of salmeterol。 in vivo: The combination of FF/VI at a strength of 100/25 μg significantly (p < 0.001) improved wm FEV1 (173 ml) and trough FEV1 (115 ml) vs. placebo. Similar effects were observed with FF/VI 50/25 μg. VI 25 μg over 24 weeks improved lung function vs. placebo significantly for wm FEV1 (103 ml, p < 0.001) and trough FEV1 (67 ml, p = 0.017) |
别名 | 维兰特罗;GW 642444X;GW 642444;GW642444X;GW642444;GW-642444X;GW-642444;4-[(R)-2-[[6-[2-(2,6-Dichlorobenzyloxy)ethoxy]hexyl]amino]-1-hydroxyethyl]-2-hydroxymethylphenol |
维兰特罗
Vilanterol (订货以英文为准)
编号:V126837
CAS号:503068-34-6
分子式:C24H33CL2NO5
分子量:486.43
产品名称 | Vilanterol |
中文名称 | 维兰特罗 |
CAS号 | 503068-34-6 |
分子式(M.F.) | C24H33CL2NO5 |
分子量(M.W.) | 486.43 |
储存条件 | -20°C储存 |
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