GSK256066

    
98%

GSK256066

源叶(MedMol)
S80958 一键复制产品信息
801312-28-7
C27H26N4O5S
518.58
6-(3-(dimethylcarbamoyl)phenylsulfonyl)-4-(3-methoxyphenylamino)-8-methylquinoline-3-carboxamide
货号 产品规格 价格(RMB) 库存(上海) 北京 武汉 南京 购买数量
S80958-5mg 98% ¥578.00 4 - - -
S80958-10mg 98% ¥1020.00 5 - - -
S80958-50mg 98% ¥3825.00 2 - - -
S80958-100mg 98% ¥6200.00 预计交期:2-3天 - - -
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

GSK256066 is a selective and high-affinity phosphodiesterase 4 (PDE4) inhibitor, with an IC50 of 3.2 pM for PDE4B. GSK256066 is developed for the research of chronic obstructive pulmonary disease

产品描述: GSK256066 is a selective and high-affinity phosphodiesterase 4 (PDE4) inhibitor, with an IC50 of 3.2 pM for PDE4B. GSK256066 is developed for the research of chronic obstructive pulmonary disease
靶点: PDE4:3.2 pM (IC50);PDE
体内研究: GSK256066 (10 μg/kg; i.t.) causes significant inhibition of LPS-induced pulmonary neutrophilia. GSK256066 also inhibits LPS-induced increases in exhaled nitric oxide (ED50=92 μg/kg). GSK256066 inhibits pulmonary eosinophilia in rats exposed to ovalbumin (ED50=0.4 μg/kg)
参考文献: 1. Tralau-Stewart CJ, et al. GSK256066, an exceptionally high-affinity and selective inhibitor of phosphodiesterase 4 suitable for administration by inhalation: in vitro, kinetic, and in vivo characterization. J Pharmacol Exp Ther, 2011, 337(1), 145-154. 2. Nials AT, et al. In vivo characterization of GSK256066, a high-affinity inhaled phosphodiesterase 4 inhibitor. J Pharmacol Exp Ther, 2011, 337(1), 137-144.
溶解性: Soluble  in  DMSO
保存条件: -20℃
配置溶液浓度参考:
1mg 5mg 10mg
1 mM 1.928 ml 9.642 ml 19.283 ml
5 mM 0.386 ml 1.928 ml 3.857 ml
10 mM 0.193 ml 0.964 ml 1.928 ml
50 mM 0.039 ml 0.193 ml 0.386 ml
注意: 部分产品我司仅能提供部分信息,我司不保证所提供信息的权威性,仅供客户参考交流研究之用。

参考文献

质检证书(COA)

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摩尔浓度计算器

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