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伊福地平

    
10mM in DMSO

Efonidipine

源叶(MedMol)
T93073 一键复制产品信息
111011-63-3
C34H38N3O7P
631.66
NZ-1053-​Pyridinecarboxylic acid,5-​(5,​5-​dimethyl-​2-​oxido-​1,​3,​2-​dioxaphosphorinan-​2-​yl)​-​1,​4-​dihydro-​2,​6-​dimethyl-​4-​(3-​nitrophenyl)​-​,2-​[phenyl(phenylmethyl​)​amino]​ethyl ester
货号 规格 价格 上海 北京 珠海 重庆 武汉 购买数量
T93073-1ml促销
10mM in DMSO

¥900.00 ¥710.00

7 - - - -
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: 钙通道抑制剂;Calcium Channel Inhibitors;;InformationEfonidipine Efonidipine (NZ-105) is an L- and T-type calcium channel blocker leading to vasodilation and decreased automaticity of the heart. It also suppresses aldosterone secretion from the adrenal.TargetsT-type calcium channelIn vitroAlthough efonidipine is not a specific T-type calcium channe (TTCC) blocker as it could also block L-type calcium channe (LTCC), its efficacy in blocking TTCC is much greater than that of LTCC. Efonidipine exerts an inhibitory effect on aldosterone synthesis and secretion in a human adrenocortical cell line (H295R), an effect that is mediated, at least in part, by suppression of 11-β-hydroxylase and aldosterone synthase expression. Efonidipine also suppresses both Ang II- and K+-induced aldosterone secretion, but it blocks the latter at much lower concentrations than the former.In vivoEfonidipine could provide broader beneficial effects including the heart, liver, and plasma, and antioxidant in iron-overload condition in both WT(muβ+⁄+) and HT(muβth-3 ⁄+,) mice.Cell Research(from reference)Cell lines:The NCI-H295R human adrenocortical cell line (H295) Concentrations:0.3 μM and 3 μM Incubation Time:24 h 
保存条件: -80℃(运输条件:冰袋低温运输)
配置溶液浓度参考:
1mg 5mg 10mg
1 mM 1.583 ml 7.916 ml 15.831 ml
5 mM 0.317 ml 1.583 ml 3.166 ml
10 mM 0.158 ml 0.792 ml 1.583 ml
50 mM 0.032 ml 0.158 ml 0.317 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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