首页 工具
登录
购物车
Rimeporide hydrochloride

Rimeporide hydrochloride

产品编号 T5333   CAS 187870-95-7
别名: 盐酸Rimeporide, EMD-87580 hydrochloride

Rimeporide hydrochloride (EMD-87580 hydrochloride) 是一种有效的 Na+/H+交换泵(NHE-1) 选择性抑制剂。

TargetMol的所有产品和服务仅用于科学研究,不能被用于人体,我们也不向个人提供产品和服务。
Rimeporide hydrochloride Chemical Structure
Rimeporide hydrochloride, CAS 187870-95-7
规格 价格/CNY 货期 数量
1 mg ¥ 1,770 现货
2 mg ¥ 2,520 现货
5 mg ¥ 3,670 现货
10 mg ¥ 5,290 现货
25 mg ¥ 8,190 现货
50 mg ¥ 10,800 现货
100 mg ¥ 14,900 现货
其他形式的 Rimeporide hydrochloride:
千万补贴 助力科研
BCA蛋白浓度测定试剂盒限时半价
重组蛋白限时优惠
产品目录号及名称: Rimeporide hydrochloride (T5333)
点击图片重新获取验证码
选择批次  
纯度: 99.84%
TargetMol batch loading
更多批次查询请联系客服
生物活性
化学信息
存储 & 溶解度
参考文献
产品描述 Rimeporide hydrochloride (EMD-87580 hydrochloride) is a potent and selective Sodium hydrogen exchange 1 (NHE-1) inhibitor.
体外活性 Treatment for 24 h with 10 μM phenylephrine significantly increased cell surface area to 129.6 3.1% of control values. The hypertrophic effect of phenylephrine was completely abrogated by 5 μM of EMD87580 [1].
细胞实验 To induce hypertrophy, myocytes were treated for 10 min or 24 h as appropriate and noted under Results with 10 μM phenylephrine in the absence or presence of the following agents: the NHE-1 inhibitor EMD87580 (5 μM) or cariporide (5 μM), the JNK1/2 inhibitor SP600125, the p38 inhibitor SB203580, the ERK1/2 inhibitor PD98059 (all at 10 μM), and the reverse mode Na+-Ca2+ exchange inhibitor KB-R7943 or SN-6 (both at 10 μM). All drugs were added 30 min before the addition of phenylephrine [1].
动物实验 Two groups were studied. The treatment group (n = 5) received EMD 87580 at a dose of 5 mg/kg IV bolus 5 min before aortic cross-clamping and 10 mol/L EMD 87580 in the cardioplegic solution. The control group (n = 9) received the same volume of saline vehicle. Systemic pretreatment was used to ensure drug availability during the ischemic period prior to CPA. Direct infusion via cardioplegia ensures drug delivery at the time of ischemia (CPA), and it decreases the variability of drug delivery that may occur during the hemodilution with CPB initiation. Incorporation into the cardioplegia also minimizes the potential variable of drug/extracorporeal circuit interactions. Using this dosing regimen, the plasma concentration of EMD 87580 was in the 2,500 to 3,000 ng/mL range at 10 min after CPB. This concentration has been shown to be effective at Na+/H+ exchanger inhibition in vitro [2].
别名 盐酸Rimeporide, EMD-87580 hydrochloride
分子量 369.84
分子式 C11H16ClN3O5S2
CAS No. 187870-95-7

存储

Powder: -20°C for 3 years | In solvent: -80°C for 1 year

溶解度

DMSO: 18.5 mg/mL (50 mM)

溶液配制表

可选溶剂 浓度 体积 质量 1 mg 5 mg 10 mg 25 mg
DMSO 1 mM 2.7039 mL 13.5194 mL 27.0387 mL 67.5968 mL
5 mM 0.5408 mL 2.7039 mL 5.4077 mL 13.5194 mL
10 mM 0.2704 mL 1.3519 mL 2.7039 mL 6.7597 mL
20 mM 0.1352 mL 0.676 mL 1.3519 mL 3.3798 mL
50 mM 0.0541 mL 0.2704 mL 0.5408 mL 1.3519 mL

TargetMol Calculator计算器

摩尔浓度计算器
稀释计算器
配液计算器
分子量计算器
=
X
X
X
=
X
=
/
g/mol

输入分子式,点击计算,可计算出产品的分子量。

TargetMol Library Books参考文献

1. Stanbouly S, et al. Sodium hydrogen exchange 1 (NHE-1) regulates connexin 43 expression in cardiomyocytes via reverse mode sodium calcium exchange and c-Jun NH2-terminal kinase-dependent pathways. J Pharmacol Exp Ther. 2008 Oct;327(1):105-13. 2. Cox CS Jr, et al. Improved myocardial function using a Na+/H+ exchanger inhibitor during cardioplegic arrest and cardiopulmonary bypass. Chest. 2003 Jan;123(1):187-94.
µ-Conotoxin BuIIIC δ-Buthitoxin-Hj2a Mambalgin-2 Hydroquinidine Valproic Acid Tetracaine hydrochloride Flecainide acetate µ-Conotoxin BuIIIA

相关化合物库

该产品包含在如下化合物库中:
抗癌药物库 抑制剂库 药物功能重定位化合物库 抗癌临床化合物库 临床期小分子药物库 经典已知活性库 已知活性化合物库 NO PAINS 化合物库 钠通道分子库 抗癌化合物库

TargetMol Calculator剂量换算

对于不同动物的给药剂量换算,您也可以参考 更多...

TargetMol Calculator 体内实验配液计算器

请在以下方框中输入您的动物实验信息后点击计算,可以得到母液配置方法和体内配方的制备方法: 比如您的给药剂量是10 mg/kg,每只动物体重20 g,给药体积100 μL,一共给药动物10 只,您使用的配方为5% DMSO+30% PEG300+5% Tween 80+60% ddH2O。那么您的工作液浓度为2 mg/mL。

母液配置方法:2 mg 药物溶于 50 μL DMSO (母液浓度为 40 mg/mL), 如您需要配置的浓度超过该产品的溶解度,请先与我们联系。

体内配方的制备方法:取 50 μL DMSO 主液,加入 300 μL PEG300, 混匀澄清,再加 50 μL Tween 80,混匀澄清,再加 600 μL ddH2O, 混匀澄清。

第一步:请输入动物实验的基本信息
剂量
mg/kg
每只动物体重
g
给药体积
μL
动物数量
第二步:请输入动物体内配方组成,不同的产品配方组成不同,如有配方需求,可先联系我们提供正确的体内配方。
% DMSO
%
% Tween 80
% ddH2O
计算 重置

技术支持

您可能有的问题的答案可以在抑制剂处理说明中找到,包括如何准备库存溶液,如何存储产品,以及基于细胞的分析和动物实验需要特别注意的问题。

Keywords

Rimeporide hydrochloride 187870-95-7 Membrane transporter/Ion channel Sodium Channel Rimeporide Hydrochloride Rimeporide EMD87580 Hydrochloride Sodium/hydrogen Exchanger 盐酸Rimeporide EMD-87580 Inhibitor EMD-87580 hydrochloride inhibit EMD87580 EMD 87580 EMD 87580 Hydrochloride Na+/H+ Exchanger (NHE) EMD-87580 Hydrochloride Sodium-hydrogen Exchanger inhibitor

 

TargetMol Loading
陶术
生物
TargetMol®中国区唯一合作伙伴
点击进入陶术生物官网陶术生物
联系我们
400-820-0310

上海市静安区江场三路238号8楼