DPI 201-106
目录号: PL11399 纯度: ≥99%
CAS No. :97730-95-5
商品编号 规格 价格 会员价 是否有货 数量
PL11399-5mg 5mg ¥964.00 请登录
PL11399-10mg 10mg ¥1607.00 请登录
PL11399-25mg 25mg ¥3214.00 请登录
PL11399-50mg 50mg ¥4821.00 请登录
PL11399-100mg 100mg ¥7232.00 请登录
PL11399-200mg 200mg 询价 询价
PL11399-500mg 500mg 询价 询价
PL11399-10mM*1mLinDMSO 10mM*1mLinDMSO ¥1060.00 请登录
Medlife所售产品仅用于科学研究(非临床研究),非药品不可食用,不可用于人体或动物的临床诊断和治疗,我们不为个人提供产品及服务。产品COA等资料,可至下方“质量控制”中下载。
中文名称
DPI 201-106
英文名称
DPI 201-106
英文别名
1H-Indole-2-carbonitrile,4-[3-[4-(diphenylmethyl)-1-piperazinyl]-2-hydroxypropoxy]-;4-[3-(4-benzhydrylpiperazin-1-yl)-2-hydroxypropoxy]-1H-indole-2-carbonitrile;SDZ-201 106 (+/-);Dpi 201-106
Cas No.
97730-95-5
分子式
C29H30N4O2
分子量
466.57
包装储存
Powder -20°C 3 years;4°C 2 years
产品详情
DPI 201-106 (SDZ 201106) 是一种心脏活性剂,具有协同肌膜和细胞内作用机制。DPI 201-106 显示电压门控钠通道 (VGSC) 的心脏选择性调节,从而产生正性肌力作用。
生物活性
DPI 201-106 (SDZ 201106) is a cardiotonic agent with a synergistic sarcolemmal and intracellular mechanism of action. DPI 201-106 shows cardioselective modulation of voltage-gated sodium channels (VGSCs) resulting in a positive inotropic effect.
性状
Solid
IC50 & Target[1][2]
Sodium Channel
体外研究(In Vitro)
DPI 201-106 increases the Ca-sensitivity of skinned fibres from porcine trabecula septomarginalis with an EC50 of 0.2 nM.
DPI 201-106 produces concentration-dependent positive inotropic effects in guinea-pig and rat left atria, kitten, rabbit and guinea-pig papillary muscles and Langendorff perfused hearts of rabbits between 0.1 and 3 μM. has not independently confirmed the accuracy of these methods. They are for reference only.
体内研究(In Vivo)
In anesthetized dogs, left ventricular dP/dtmax is increased by DPI 201-106 0.2 mg/kg i.v.In digoxin-pretreated anesthetized cats, DPI 201-106 is infused up to an accumulated dose of 12.22 mg/kg i.v. . has not independently confirmed the accuracy of these methods. They are for reference only.
运输条件
Room temperature in continental US; may vary elsewhere.
储存方式
Powder -20°C 3 years;4°C 2 years
参考文献
[1]. G Scholtysik, et al. DPI 201-106, a novel cardioactive agent. Combination of cAMP-independent positive inotropic, negative chronotropic, action potential prolonging and coronary dilatory properties. Naunyn Schmiedebergs Arch Pharmacol.1985 May;329(3):316-
[2]. G Scholtysik, et al. Interaction of DPI 201-106 with cardiac glycosides. J Cardiovasc Pharmacol. 1989 Feb;13(2):342-7.
溶解度数据
In Vitro: DMSO : 250 mg/mL (535.83 mM; Need ultrasonic)配制储备液
搜索质检报告(COA)

1:一般建议:溶解度为Medlife测试数据,可能与文献描述存在差异。这是由于生产工艺和批次不同产生的正常现象。为了使其更好的溶解,请用37℃加热试管并在超声波水浴中震动片刻。不同批次产品溶解度各有差异,仅做参考,具体以实验方案为准。

2:储存条件:粉末-20°C一般情况可以保存3年,溶于溶剂-80°C一般情况可以保存1年。不同产品及不同批次产品可能存在差异,请细致阅读产品信息,并辅助参考相关文献描述。

The molarity calculator equation
Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)
The dilution calculator equation
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)
This equation is commonly abbreviated as: C1V1 = C2V2