1. Others Membrane Transporter/Ion Channel Neuronal Signaling
  2. Isotope-Labeled Compounds Calcium Channel
  3. Barnidipine-d5 hydrochloride

Barnidipine-d5 hydrochloride  (Synonyms: Mepirodipine-d5 hydrochloride; YM-09730-5-d5 hydrochloride)

目录号: HY-107322S 纯度: ≥98.0%
COA 产品使用指南

Barnidipine-d5 (hydrochloride) 是 Barnidipine hydrochloride 的氘代物。Barnidipine (Mepirodipine) hydrochloride 巴尼地平是一种 L 型钙拮抗剂 (CaA),对 [3H] initrendipine 结合位点具有高亲和力 (Ki=0.21 nmol/l),对 CaA 受体具有选择性作用。Barnidipine (Mepirodipine) hydrochloride 是一种抗高血压活性分子,通过减少其血管扩张作用继发的外周血管阻力起作用。

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Barnidipine-d<sub>5</sub> hydrochloride Chemical Structure

Barnidipine-d5 hydrochloride Chemical Structure

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规格 价格 是否有货 数量
1 mg ¥5500
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Other Forms of Barnidipine-d5 hydrochloride:

  • 生物活性

  • 纯度 & 产品资料

  • 参考文献

生物活性

Barnidipine-d5 (hydrochloride) is the deuterium labeled Barnidipine hydrochloride. Barnidipine hydrochloride (Mepirodipine hydrochloride) is an L-type calcium antagonist (CaA) with high affinity for [3H] initrendipine binding sites (Ki=0.21 nmol/l), has selective action against CaA receptors[1].Barnidipine hydrochloride (Mepirodipine hydrochloride) is an antihypertensive agent and acts by the reduction of peripheral vascular resistance secondary to its vasodilatory action[2].

IC50 & Target

L-type calcium channel

 

体外研究
(In Vitro)

Stable heavy isotopes of hydrogen, carbon, and other elements have been incorporated into drug molecules, largely as tracers for quantitation during the drug development process. Deuteration has gained attention because of its potential to affect the pharmacokinetic and metabolic profiles of drugs[1].

MCE has not independently confirmed the accuracy of these methods. They are for reference only.

分子量

533.03

Formula

C27H25D5ClN3O6

性状

固体

颜色

Off-white to light yellow

中文名称

盐酸巴尼地平 d5 (盐酸盐)

运输条件

Room temperature in continental US; may vary elsewhere.

储存方式

-20°C, sealed storage, away from moisture

*In solvent : -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture)

溶解性数据
In Vitro: 

DMSO 中的溶解度 : 250 mg/mL (469.02 mM; 超声加热助溶; 吸湿的 DMSO 对产品的溶解度有显著影响,请使用新开封的 DMSO)

配制储备液
浓度 溶剂体积 质量 1 mg 5 mg 10 mg
1 mM 1.8761 mL 9.3803 mL 18.7607 mL
5 mM 0.3752 mL 1.8761 mL 3.7521 mL
查看完整储备液配制表

* 请根据产品在不同溶剂中的溶解度选择合适的溶剂配制储备液;一旦配成溶液,请分装保存,避免反复冻融造成的产品失效
储备液的保存方式和期限:-80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture)。-80°C储存时,请在6个月内使用,-20°C储存时,请在1个月内使用。

  • 摩尔计算器

  • 稀释计算器

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

质量
=
浓度
×
体积
×
分子量 *

Concentration (start) × Volume (start) = Concentration (final) × Volume (final)

This equation is commonly abbreviated as: C1V1 = C2V2

浓度 (start)

C1

×
体积 (start)

V1

=
浓度 (final)

C2

×
体积 (final)

V2

动物溶解方案计算器
请输入动物实验的基本信息:

给药剂量

mg/kg

动物的平均体重

g

每只动物的给药体积

μL

动物数量

由于实验过程有损耗,建议您多配一只动物的量
计算结果
工作液所需浓度 : mg/mL
纯度 & 产品资料

纯度: ≥98.0%

参考文献

完整储备液配制表

* 请根据产品在不同溶剂中的溶解度选择合适的溶剂配制储备液;一旦配成溶液,请分装保存,避免反复冻融造成的产品失效
储备液的保存方式和期限:-80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture)。-80°C储存时,请在6个月内使用,-20°C储存时,请在1个月内使用。

可选溶剂 浓度 溶剂体积 质量 1 mg 5 mg 10 mg 25 mg
DMSO 1 mM 1.8761 mL 9.3803 mL 18.7607 mL 46.9017 mL
5 mM 0.3752 mL 1.8761 mL 3.7521 mL 9.3803 mL
10 mM 0.1876 mL 0.9380 mL 1.8761 mL 4.6902 mL
15 mM 0.1251 mL 0.6254 mL 1.2507 mL 3.1268 mL
20 mM 0.0938 mL 0.4690 mL 0.9380 mL 2.3451 mL
25 mM 0.0750 mL 0.3752 mL 0.7504 mL 1.8761 mL
30 mM 0.0625 mL 0.3127 mL 0.6254 mL 1.5634 mL
40 mM 0.0469 mL 0.2345 mL 0.4690 mL 1.1725 mL
50 mM 0.0375 mL 0.1876 mL 0.3752 mL 0.9380 mL
60 mM 0.0313 mL 0.1563 mL 0.3127 mL 0.7817 mL
80 mM 0.0235 mL 0.1173 mL 0.2345 mL 0.5863 mL
100 mM 0.0188 mL 0.0938 mL 0.1876 mL 0.4690 mL
Help & FAQs
  • Do most proteins show cross-species activity?

    Species cross-reactivity must be investigated individually for each product. Many human cytokines will produce a nice response in mouse cell lines, and many mouse proteins will show activity on human cells. Other proteins may have a lower specific activity when used in the opposite species.

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产品名称:
Barnidipine-d5 hydrochloride
目录号:
HY-107322S
需求量: