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Merck

N149

Sigma-Aldrich

尼莫地平

别名:

1,4-二氢-2,6-二甲基-4-(3-硝基苯基)-3,5-吡啶二甲酸-2-甲氧基乙基1-甲基乙基酯, 1,4-二氢-2,6-二甲基-4-(间硝基苯基)-3,5-吡啶二甲酸异丙酯-2-甲氧基乙酯

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100 MG
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100 MG
$155.00
500 MG
$607.00

About This Item

经验公式(希尔记法):
C21H26N2O7
CAS号:
分子量:
418.44
EC 号:
MDL编号:
UNSPSC代码:
12352200
PubChem化学物质编号:
NACRES:
NA.77

$155.00


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方案

≥98% (HPLC)

质量水平

表单

powder

颜色

off-white to yellow

溶解性

methanol: 62.5 mg/mL
45% (w/v) aq 2-hydroxypropyl-β-cyclodextrin: insoluble
H2O: insoluble

创始人

Bayer

SMILES字符串

COCCOC(=O)C1=C(C)NC(C)=C(C1c2cccc(c2)[N+]([O-])=O)C(=O)OC(C)C

InChI

1S/C21H26N2O7/c1-12(2)30-21(25)18-14(4)22-13(3)17(20(24)29-10-9-28-5)19(18)15-7-6-8-16(11-15)23(26)27/h6-8,11-12,19,22H,9-10H2,1-5H3

InChI key

UIAGMCDKSXEBJQ-UHFFFAOYSA-N

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应用

尼莫地平已被用于:
  • 作为L型钙通道(LTCC)的抑制剂,以评估其在振动切割中的神经保护活性[1]
  • 作为标准品,用于通过高效液相色谱(HPLC)对手性药物进行对映体分离[2]
  • 测量脊柱电压逃逸的药理学研究[3]

生化/生理作用

尼莫地平可增强黑质多巴胺能神经元的存活。[1]
尼莫地平是一种有效的L型Ca2+ 通道拮抗剂。

特点和优势

该化合物在受体分类和信号转导手册的钙通道页面上有重点介绍。如需浏览其他手册页面,请点击此处
该化合物由Bayer开发。要浏览其他药物开发化合物和批准的药物/候选药物列表,单击此处

注意

光敏性

象形图

Exclamation mark

警示用语:

Warning

危险声明

危险分类

Acute Tox. 4 Oral

储存分类代码

11 - Combustible Solids

WGK

WGK 1

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

dust mask type N95 (US), Eyeshields, Gloves


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Ester Ponzetto et al.
Journal of neurosurgery, 119(5), 1125-1128 (2013-08-27)
The authors describe a rare case of central auditory dysfunction induced by cerebral vasospasm after aneurysmal subarachnoid hemorrhage (SAH). A 55-year-old woman who was admitted after aneurysmal SAH developed cerebral vasospasm on Day 3 affecting mainly the right middle cerebral
Yuri C Martins et al.
Malaria journal, 12, 138-138 (2013-04-27)
Human cerebral malaria (HCM) is a life-threatening complication caused by Plasmodium falciparum infection that continues to be a major global health problem despite optimal anti-malarial treatment. In the experimental model of cerebral malaria (ECM) by Plasmodium berghei ANKA, bolus administration
Dendritic spines prevent synaptic voltage clamp
Beaulieu-Laroche L and Harnett MT
Neuron, 97(1), 75-82 (2018)
Karen F S Bell et al.
Journal of neurochemistry, 126(2), 274-287 (2013-02-01)
NMDA-type glutamate receptors mediate both trophic and excitotoxic signalling in CNS neurons. We have previously shown that blocking NMDAR- post-synaptic density-95 (PSD95) interactions provides significant protection from excitotoxicity and in vivo ischaemia; however, the mechanism of neuroprotection is unclear. Here
J Horn et al.
Stroke, 32(10), 2433-2438 (2001-10-06)
Based on the results of animal experiments, clinical trials were performed with nimodipine, which did not demonstrate a beneficial effect on outcome after stroke. The aim of this study was to determine whether the evidence from animal experiments with nimodipine

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