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PCS1055 dihydrochloride

    
≥98%

源叶(MedMol)
V46736 一键复制产品信息
361979-40-0
C27H34Cl2N4
485.49
货号 规格 价格 上海 北京 珠海 重庆 武汉 购买数量
V46736-1mg
≥98%

¥2110.00

货期:3-5天 - - - -
V46736-5mg
≥98%

¥4990.00

货期:3-5天 - - - -
V46736-10mg
≥98%

¥7980.00

货期:3-5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
产品描述: PCS1055 dihydrochloride is a potent, selective and competitive muscarinic M4 receptor antagonist with an IC50 of 18.1 nM and a Kd of 5.72 nM. PCS1055 dihydrochloride inhibits radioligand [3H]-NMS binding to the M4 receptor with a Ki of 6.5 nM. PCS1055 dihydrochloride exhibits >100-fold selectivity over M1-, M3-, and M5-receptors and 30-fold selectivity at the M2 receptor. PCS1055 dihydrochloride is also a potent AChE inhibitor with IC50 s of 22 nM and 120 nM for electric eel and human AChE, respectively.
体外研究: PCS1055 also antagonized functional signal transduction as demonstrates by the inhibition of agonist-stimulated GTP-γ-[35S] binding. PCS1055 inhibits G protein activation in a concentration dependent manner, with the highest potency at the M4 receptors. Both studies shows that PCS1055 is most potent at the M4 receptor subtype with a binding preference of 130-, 31.2-, 426- and >1000-fold, and functional preference of 255-, 69.1-, 342- and >1000-fold over the M1-, M2-, M3- and M5 receptors, respectively.
保存条件: 2-8°C, 干燥
配置溶液浓度参考:
1mg 5mg 10mg
1 mM 2.06 ml 10.299 ml 20.598 ml
5 mM 0.412 ml 2.06 ml 4.12 ml
10 mM 0.206 ml 1.03 ml 2.06 ml
50 mM 0.041 ml 0.206 ml 0.412 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

质量 (mg) = 浓度 (mM) x 体积 (mL) x 分子摩尔量 (g/mol)

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