Salmeterol xinafoate

    97%

Salmeterol xinafoate

源叶(MedMol)
S81155
94749-08-3
C36H45NO7
603.74
昔美酸沙美特罗;苯磺阿曲库铵;葛兰素威;2-羟甲基-4-[1-羟基-2-[6-(4-苯基丁氧基)己基氨基]乙基]苯酚 1-羟基-2-萘甲酸盐;沙美特罗羟萘甲酸盐;昔美酸沙美特罗;沙美特罗羟萘甲酸盐/2-羟甲基-4-[1-羟基-2-[6-(4-苯基丁氧基)己基氨基]乙基]苯酚 1-羟基-2-萘甲酸盐;甲醇中沙米特罗溶液标准物质;沙美特罗羟萘甲酸盐:昔美酸沙美特罗;(+/-) 4-HYDROXY-A1
品牌 货号 产品规格 价格(RMB) 库存(上海) 北京 武汉 南京 购买数量
源叶(MedMol) S81155-10mg 97% ¥560.00元 7 - - -
源叶(MedMol) S81155-50mg 97% ¥1680.00元 6 - - -
源叶(MedMol) S81155-250mg 97% ¥4400.00元 4 - - -
产品介绍 参考文献 质检证书(COA) 摩尔浓度计算器 相关产品

产品介绍

Salmeterol (GR 33343X) xinafoate is a potent and selective human β2 adrenoceptor agonist. Salmeterol shows potent stimulation of cAMP accumulation in CHO cells expressing human β2, β1 and β3 adrenoceptors with pEC50s of 9.6, 6.1, and 5.9, respectively
产品描述: Salmeterol (GR 33343X) xinafoate is a potent and selective human β2 adrenoceptor agonist. Salmeterol shows potent stimulation of cAMP accumulation in CHO cells expressing human β2, β1 and β3 adrenoceptors with pEC50s of 9.6, 6.1, and 5.9, respectively
靶点: β2 adrenoceptor:9.6 (pEC50);β1 adrenoceptor:6.1 (pEC50);β3 adrenoceptor:5.9 (pEC50);HIVProtease; AdrenergicReceptor
体内研究: Salmeterol (0.16 mg/kg), Formoterol (0.32 mg/kg) and combined treatment have therapeutic effects in mice with chronic obstructive pulmonary disease (COPD)
参考文献: 1. Panayiotis A Procopiou, et al. The discovery of long-acting saligenin β₂ adrenergic receptor agonists incorporating a urea group. Bioorg Med Chem. 2011 Oct 15;19(20):6026-32. 2. Malcolm Johnson. Effects of beta2-agonists on resident and infiltrating inflammatory cells. J Allergy Clin Immunol. 2002 Dec;110(6 Suppl):S282-90. 3. Zhiyuan Wang, et al. Efficacy of salmeterol and formoterol combination treatment in mice with chronic obstructive pulmonary disease. Exp Ther Med. 2018 Feb;15(2):1538-1545.
溶解性: DMSO  :  ≥  50  mg/mL  (82.82  mM)
保存条件: 2-8℃
配置溶液浓度参考:
1mg 5mg 10mg
1 mM 1.656 ml 8.282 ml 16.563 ml
5 mM 0.331 ml 1.656 ml 3.313 ml
10 mM 0.166 ml 0.828 ml 1.656 ml
50 mM 0.033 ml 0.166 ml 0.331 ml
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参考文献

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摩尔浓度计算器

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