中文名称: | Nicardipine 一键复制产品信息 | ||||
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英文名称: | Nicardipine | ||||
别名: | 尼卡地平 YC-93freebase | ||||
CAS No: | 55985-32-5 | 分子式: | C26H29N3O6 | 分子量: | 479.53 |
CAS No: | 55985-32-5 | ||||
分子式: | C26H29N3O6 | ||||
分子量: | 479.53 | ||||
EINEC: | 259-932-3 | ||||
EINEC: | 259-932-3 |
基本信息
产品编号: |
N11018 |
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产品名称: |
Nicardipine |
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CAS: |
55985-32-5 |
储存条件 |
粉末 |
2-8℃ |
四年 |
分子式: |
溶于液体 |
-80℃ |
一年 |
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分子量: |
479.53 |
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化学名: |
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Solubility (25°C): |
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体外:
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DMSO |
95mg/mL (198.11mM) |
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Ethanol |
95mg/mL (198.11mM) |
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Water |
30mg/mL (62.56mM) |
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体内(现配现用): |
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<1mg/ml表示微溶或不溶。 |
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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。 |
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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。 |
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靶点 |
IC50:1μM (cardiac calcium channels) |
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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 |
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Cell Line: |
VSMCs were isolated from New Zealand rabbit aortic preparations |
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Concentration: |
0.1μM,1μM,3μM,10μM |
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Incubation Time: |
24-48 hours |
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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. |
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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. |
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Animal Model: |
In conscious normotensive rats (NR) |
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Dosage: |
0.3-10mg/kg |
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Administration: |
P.o. |
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Result: |
Induced a dose-dependent hypotensive response (maximal decrease in mean blood pressure, supine position) without any postural hypotensive response. |
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
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 )