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安全信息

M0821

Sigma-Aldrich

Moexipril 盐酸盐

powder, ≥98% (HPLC)

别名:

(3S)-2-[(2S)-2-[[(1S)-1-(Ethoxycarbonyl)-3-phenylpropyl]amino]-1-oxopropyl]-1,2,3,4-tetrahydro-6,7-dimethoxy-3-isoquinolinecarboxylic acid 盐酸盐

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About This Item

经验公式（希尔记法）:
C27H35N2O7Cl
CAS号:
82586-52-5
分子量:
535.03
MDL编号:
MFCD00940481
UNSPSC代码:
12352200
PubChem化学物质编号:
329817832
NACRES:
NA.77

质量水平

100

方案

≥98% (HPLC)

表单

powder

溶解性

H2O: 32 mg/mL

创始人

UCB Inc.

储存温度

2-8°C

SMILES字符串

Cl.CCOC(=O)[C@H](CCc1ccccc1)N[C@@H](C)C(=O)N2Cc3cc(OC)c(OC)cc3C[C@H]2C(O)=O

InChI

1S/C27H34N2O7.ClH/c1-5-36-27(33)21(12-11-18-9-7-6-8-10-18)28-17(2)25(30)29-16-20-15-24(35-4)23(34-3)14-19(20)13-22(29)26(31)32;/h6-10,14-15,17,21-22,28H,5,11-13,16H2,1-4H3,(H,31,32);1H/t17-,21-,22-;/m0./s1

InChI key

JXRAXHBVZQZSIC-JKVLGAQCSA-N

基因信息

human ... ACE(1636)

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生化/生理作用

ACE-Inhibitor; Antihypertensive
Moexipril is an ACE-Inhibitor; Antihypertensive; Unlike other ACE inhibitors, prolongs QT interval leading to torsades de pointes and cardiad arrhythmia;

特点和优势

This compound is featured on the Angiotensin Receptors page of the Handbook of Receptor Classification and Signal Transduction. To browse other handbook pages, click here.
This compound was developed by UCB Inc.. To browse the list of other pharma-developed compounds and Approved Drugs/Drug Candidates, click here.

象形图

Environment
GHS09

警示用语：

Warning

危险声明

H400

预防措施声明

P273 - P391 - P501

危险分类

Aquatic Acute 1

储存分类代码

11 - Combustible Solids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

Eyeshields, Gloves

法规信息

新产品

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number
0000318459
0000303273
0000318459
0000303273
0000137115

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The EMBO journal, 29(1), 222-235 (2009-11-21)
It has been suggested that intrinsic brain tumours originate from a neural stem/progenitor cell population in the subventricular zone of the post-natal brain. However, the influence of the initial genetic mutation on the phenotype as well as the contribution of
K E Kristensen et al.
Clinical pharmacology and therapeutics, 96(6), 713-722 (2014-09-16)
Clopidogrel is an oral antiplatelet prodrug, the majority of which is hydrolyzed to an inactive metabolite by hepatic carboxylesterase 1 (CES1). Most angiotensin-converting enzyme inhibitors (ACEIs) are also metabolized by this enzyme. We examined the effects of ACEIs on clopidogrel

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