中文名称: Nicardipine  一键复制产品信息
英文名称: Nicardipine
CAS No: 55985-32-5
分子式: C26H29N3O6
分子量: 479.53
EINEC: 259-932-3
N11018 Nicardipine ≥98% (普西唐-psaitong)
包装规格:
100mg 250mg 1g in glass bottle
产品描述:

基本信息

产品编号:

N11018

产品名称:

Nicardipine

CAS:

55985-32-5

 

储存条件

粉末

2-8℃

四年

分子式:

C26H29N3O6

溶于液体

-80℃

一年

分子量:

479.53

 

 

化学名: 

3,5-Pyridinedicarboxylic acid,1,4-dihydro-2,6-dimethyl-4-(3-nitrophenyl)-,methyl 2-(methyl(phenylmethyl)amino)ethyl ester

Solubility (25°C):

 

体外:

 

DMSO

95mg/mL (198.11mM)

Ethanol

95mg/mL (198.11mM)

Water

30mg/mL (62.56mM)

体内(现配现用):

 

1mg/ml表示微溶或不溶。

普西唐提供的所有化合物浓度为内部测试所得,实际溶液度可能与公布值有所偏差,属于正常的批间细微差异现象。

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。

 

制备储备液

 

浓度

 

溶液体积

质量

 

1mg

 

5mg

 

10mg

1mM

2.0854mL

10.4271mL

20.8542mL

5mM

0.4171mL

2.0854mL

4.1708mL

10mM

0.2085mL

1.0427mL

2.0854mL

 

生物活性

产品描述

一种钙通道(calciumchannel)阻滞剂,可阻断心脏钙通道,IC50为1μM。Nicardipine可用于研究慢性心绞痛以及控制血压。

靶点

IC50:1μM (cardiac calcium channels)

体外研究

Nicardipine (0.1-10μM;24-48h) reduces viability and proliferation of vascular smooth muscle cells (VSMCs) and inhibits their ability to migrate.

Cell Viability Assay

Cell Line:

VSMCs were isolated from New Zealand rabbit aortic preparations

Concentration:

0.1μM,1μM,3μM,10μM

Incubation Time:

24-48 hours

Result:

Treatment reduced significantly cell viability and inhibited VSMCs proliferation in the presence of 10% FBS in a dose-dependent way,from 205.4±17.5% to 176.6±17%,160.6±5.7%,150.4±11.2%,61.22±7.83% after 0.1μM,1μM,3μM,10μM treatment,respectively.

体内研究

Nicardipine (0.3-10mg/kg;p.o.) shows antihypertensive properties.LD50s of Nicardipine are 643mg/kg (oral) and 557mg/kg (oral);18.1mg/kg (intravenous) 25.0mg/kg (intravenous);735mg/kg (subcutaneous) and 683mg/kg (subcutaneous);171mg/kg (intraperitoneally) and 155mg/kg (intraperitoneally) for male and female Sprague-Dawley rats, respectively.LD50s of Nicardipine are 187mg/kg (oral) and 15.5mg/kg (intravenous) for male Wistar rats,respectively.LD50s of Nicardipine are 634mg/kg (oral) and 650mg/kg (oral);20.7mg/kg (intravenous) 19.9mg/kg (intravenous);540mg/kg (subcutaneous) and 710mg/kg (subcutaneous);144mg/kg (intraperitoneally) and 161mg/kg (intraperitoneally) for male and female mice,respectively.

Animal Model:

In conscious normotensive rats (NR)

Dosage:

0.3-10mg/kg

Administration:

P.o.

Result:

Induced a dose-dependent hypotensive response (maximal decrease in mean blood pressure, supine position) without any postural hypotensive response.

保存条件:
2-8℃
UN码:
HazardClass:
危害声明:
安全说明:
搜索质检报告(COA)

本计算器可帮助您计算出特定溶液中溶质的质量、溶液浓度和体积之间的关系,公式为:
质量 (g) = 浓度 (mol/L) x 体积 (L) x 分子量 (g/mol)

摩尔浓度计算公式

  • =
    *
    *
    *选择对应的单位 *空出希望得到的变量,填写另外两个变量

用本工具协助配置特定浓度的溶液,使用的计算公式为:
开始浓度 x 开始体积 = 最终浓度 x 最终体积

稀释公式

稀释公式一般简略地表示为:C1V1 = C2V2 ( 输入 输出 )

  • * = *

连续稀释计算器方程

  • 连续稀释

  • 初始浓度:
  • 稀释倍数:
  • 计算结果

  • C1=C0/X C1: LOG(C1):
    C2=C1/X C2: LOG(C2):
    C3=C2/X C3: LOG(C3):
    C4=C3/X C4: LOG(C4):
    C5=C4/X C5: LOG(C5):
    C6=C5/X C6: LOG(C6):
    C7=C6/X C7: LOG(C7):
    C8=C7/X C8: LOG(C8):