首页 工具
登录
购物车
Barnidipine hydrochloride

Barnidipine hydrochloride

产品编号 T5856   CAS 104757-53-1
别名: 盐酸巴尼地平, YM-09730-5 hydrochloride, Mepirodipine (hydrochloride)

Barnidipine hydrochloride (YM-09730-5 hydrochloride) 是一种二氢吡啶类钙通道阻滞剂,对 CaA 受体具有选择性作用。它是一种抗高血压药物,通过减少其血管扩张作用继发的外周血管阻力起作用。

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。
Barnidipine hydrochloride Chemical Structure
Barnidipine hydrochloride, CAS 104757-53-1
规格 价格/CNY 货期 数量
1 mg ¥ 215 现货
5 mg ¥ 489 现货
10 mg ¥ 788 现货
25 mg ¥ 975 现货
50 mg ¥ 1,160 现货
100 mg ¥ 1,680 现货
200 mg ¥ 2,530 现货
1 mL * 10 mM (in DMSO) ¥ 867 现货
其他形式的 Barnidipine 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: Barnidipine hydrochloride (T5856)
点击图片重新获取验证码
选择批次  
纯度: 98%
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 Barnidipine hydrochloride (YM-09730-5 hydrochloride) is a dihydropyridine calcium channel blocker that has an IC50 value of 0.35 nM in potassium-induced tonic contraction of pig coronary artery
靶点活性 [3H]-Initrendipine:0.21 nmol/l (Ki)
体内活性 Barnidipine demonstrates antihypertensive activity by reducing peripheral vascular resistance. It decreases blood pressure in spontaneously hypertensive rats when administered orally at 1 and 3 mg/kg per day[1]. Formulations containing barnidipine have been used as a treatment for hypertension. In obstructive sleep apnea patients with non-dipper pattern hypertension, barnidipine reduced mean nighttime systolic and diastolic arterial blood pressure[2].
动物实验 Forty-one patients (mean age 69 ± 17 years, 18 females) with previously diagnosed OSA (by reduced channel home-based polysomnography) who were not being treated with continuous positive airway pressure (CPAP) because of contraindications or because of patient intolerance or rejection were evaluated. Non-dipper status was defined as the presence of a nighttime fall in systolic blood pressure (BP) which was < 10% that of daytime systolic BP as observed in a previous ambulatory blood pressure (ABP) monitoring. OSA was defined according to the presence of 5 or more episodes per hour of apnoea, hypopnoea or arousal due to respiratory effort. The reproducibility of non-dipping status was confirmed through a second 24-h ABP monitoring performed at baseline. On top of the previous stable treatment regimen (which excluded calcium-channel blockers), a 10 mg dosing of barnidipine hydrochloride at bedtime was added to all subjects during a 12-week period[2].
别名 盐酸巴尼地平, YM-09730-5 hydrochloride, Mepirodipine (hydrochloride)
分子量 528
分子式 C27H30ClN3O6
CAS No. 104757-53-1

存储

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

溶解度

DMSO: 250 mg/mL (473.48 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 1.8939 mL 9.4697 mL 18.9394 mL 47.3485 mL
5 mM 0.3788 mL 1.8939 mL 3.7879 mL 9.4697 mL
10 mM 0.1894 mL 0.947 mL 1.8939 mL 4.7348 mL
20 mM 0.0947 mL 0.4735 mL 0.947 mL 2.3674 mL
50 mM 0.0379 mL 0.1894 mL 0.3788 mL 0.947 mL
100 mM 0.0189 mL 0.0947 mL 0.1894 mL 0.4735 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. Kawashima K , Toda H , Oohata H , et al. Antihypertensive and diuretic effects of YM-09730-5, a new calcium antagonist, in stroke-prone spontaneously hypertensive rats[J]. Gen Pharmacol, 1991, 22(2):263-266. 2. Giuseppe C , Luisa F M , Antonino C , et al. Effect of Bedtime Dosing of Barnidipine Hydrochloride in Nondipper Hypertensive Patients with Obstructive Sleep Apnoea not Treated with Continuous Positive Airway Pressure[J]. Journal of Clinical Hypertension, 2013, 15(2):339.
wt hMLN Tetrandrine ω-Conotoxin SO3 Calcium Channel antagonist 4 Norverapamil Calcium Channel antagonist 3 Catharanthine 7Beta-Hydroxycholesterol

相关化合物库

该产品包含在如下化合物库中:
抗癌上市药物库 抗癌药物库 药物功能重定位化合物库 膜蛋白靶向化合物库 离子通道库 抗心血管疾病化合物库 抗高血压化合物库 上市药物库 NO PAINS 化合物库 经典已知活性库

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

Barnidipine hydrochloride 104757-53-1 Membrane transporter/Ion channel Metabolism Calcium Channel Mepirodipine 盐酸巴尼地平 Ca2+ channels inhibit Barnidipine YM-09730-5 hydrochloride Inhibitor Ca channels Barnidipine Hydrochloride Mepirodipine (hydrochloride) YM-09730-5 Hydrochloride 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