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培哚普利

更新时间:2025-08-21 08:34:40

培哚普利结构式
培哚普利结构式
品牌特惠专场
常用名 培哚普利 英文名 Perindopril erbumine
CAS号 107133-36-8 分子量 441.605
密度 1.15 g/cm3 沸点 537.4ºC at 760mmHg
分子式 C23H43N3O5 熔点 126-128ºC
MSDS 中文版 美版 闪点 278.8ºC

 培哚普利用途


【用途1】
用于治疗高血压、充血性心力衰竭等病症

 培哚普利名称

中文名 培哚普利叔丁胺盐
英文名 perindopril erbumine
中文别名 培哚 | 培哚普利
英文别名 更多

 培哚普利物理化学性质

密度 1.15 g/cm3
沸点 537.4ºC at 760mmHg
熔点 126-128ºC
分子式 C23H43N3O5
分子量 441.605
闪点 278.8ºC
精确质量 441.320282
PSA 121.96000
LogP 3.71330
InChIKey IYNMDWMQHSMDDE-MHXJNQAMSA-N
SMILES CC(C)(C)N.CCCC(NC(C)C(=O)N1C(C(=O)O)CC2CCCCC21)C(=O)OCC
外观性状 白色固体
储存条件 -20°C Freezer
水溶解性 H2O: soluble10mg/mL, clear

 培哚普利安全信息

个人防护装备 Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter
危害码 (欧洲) Xi
风险声明 (欧洲) R36/37/38
安全声明 (欧洲) 26-36
危险品运输编码 NONH for all modes of transport
RTECS号 NL5999600

 培哚普利合成线路

~95%

培哚普利结构式

培哚普利

107133-36-8

文献:Dubuffet, Thierry; Lecouve, Jean-Pierre Patent: US2007/43103 A1, 2007 ; Location in patent: Page/Page column 2 ;

~62%

培哚普利结构式

培哚普利

107133-36-8

文献:KRKA, tovarna zdravil, d.d., Novo mesto Patent: EP1792896 A1, 2007 ; Location in patent: Page/Page column 7-8 ;

~91%

培哚普利结构式

培哚普利

107133-36-8

文献:QUIMICA SINTETICA, S.A. Patent: WO2006/70276 A1, 2006 ; Location in patent: Page/Page column 8 ;

~%

培哚普利结构式

培哚普利

107133-36-8

文献:WO2006/137082 A1, ; Page/Page column 11-12 ;

~94%

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培哚普利

107133-36-8

文献:Dubuffet, Thierry; Lecouve, Jean-Pierre Patent: US2006/178421 A1, 2006 ; Location in patent: Page/Page column 2 ;

~%

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107133-36-8

文献:US2006/211867 A1, ; Page/Page column 4 ;

~%

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培哚普利

107133-36-8

文献:US2006/211867 A1, ; Page/Page column 3-4 ;

 培哚普利文献41

更多文献
Clopidogrel bioactivation and risk of bleeding in patients cotreated with angiotensin-converting enzyme inhibitors after myocardial infarction: a proof-of-concept study.

Clin. Pharmacol. Ther. 96(6) , 713-22, (2014)

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) a...

Precision-cut liver slices as a model for the early onset of liver fibrosis to test antifibrotic drugs.

Toxicol. Appl. Pharmacol. 274(2) , 328-38, (2014)

Induction of fibrosis during prolonged culture of precision-cut liver slices (PCLS) was reported. In this study, the use of rat PCLS was investigated to further characterize the mechanism of early ons...

Hepatic, intestinal, renal, and plasma hydrolysis of prodrugs in human, cynomolgus monkey, dog, and rat: implications for in vitro-in vivo extrapolation of clearance of prodrugs.

Drug Metab. Dispos. 42(9) , 1522-31, (2014)

Hydrolysis plays an important role in metabolic activation of prodrugs. In the current study, species and in vitro system differences in hepatic and extrahepatic hydrolysis were investigated for 11 pr...

 培哚普利靶点实验

查看更多实验

实验名称:ERK5 transcriptional activity HTS
来源:24565
靶标:N/A
External Id:ERK5 transcriptional activity-HTS
实验名称:A screen for compounds that inhibit the activity of LtaS in Staphylococcus aureus
来源:ICCB-Longwood/NSRB Screening Facility, Harvard Medical School
External Id:HMS979
实验名称:Identifying Sarm1 Tir Hydrolase inhibitors through NAD-Glo assay
来源:24386
靶标:N/A
External Id:Sarm1 Tir NADase inhibitors screen
实验名称:Increase the activity of the Burkholderia fixLJ 2-component system
来源:ICCB-Longwood/NSRB Screening Facility, Harvard Medical School
靶标:Burkholderia multivorans
External Id:HMS1625
实验名称:qHTS assay to identify small molecule agonists of the TGF-beta/Smad signaling pathway...
来源:824
靶标:N/A
External Id:TGF788
实验名称:qHTS assay to identify small molecule antagonists of the TGF-beta/Smad signaling path...
来源:824
靶标:N/A
External Id:TGF602
实验名称:p53 small molecule agonists, cell-based qHTS assay: qHTS cell viability counter scree...
来源:824
靶标:N/A
External Id:P53600
实验名称:p53 small molecule agonists, cell-based qHTS assay with rat liver microsomes: qHTS ce...
来源:824
靶标:N/A
External Id:P53MS958
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 培哚普利英文别名

Aceon
S 9490-3
PrestariuM
(2S,3aS,7aS)-1-[(2S)-2-{[(1S)-1-(ethoxycarbonyl)butyl]amino}propanoyl]octahydro-1H-indole-2-carboxylic acid - 2-methylpropan-2-amine (1:1) (non-preferred name)
(2S,3aS,7aS)-1-[(2S)-2-{[(2S)-1-Ethoxy-1-oxopentan-2-yl]amino}propanoyl]octahydro-1H-indole-2-carboxylic acid - 2-methylpropan-2-amine (1:1) (non-preferred name)
acide (2S,3aS,7aS)-1-[(2S)-2-{[(1S)-1-(éthoxycarbonyl)butyl]amino}propanoyl]octahydro-1H-indole-2-carboxylique - 2-méthylpropan-2-amine (1:1)
McN-A 2833-109
McN-A-2833-109
Perinodpril ErbiMune
ButylaMiniperindopril
Perindoril
Perindopril erbumine
MFCD02313824
Perindopril tert-butylamine
(2S,3aS,7aS)-1-[(2S)-2-{[(2S)-1-Ethoxy-1-oxo-2-pentanyl]amino}propanoyl]octahydro-1H-indole-2-carboxylic acid - 2-methyl-2-propanamine (1:1)
S-9490-3
Perindopril t-Butylamine Salt
(2S,3aS,7aS)-1-((S)-N-((S)-1-Carboxybutyl)alanyl)hexahydro-2-indolinecarboxylic Acid 1-Ethyl Ester compound with tert-Butylamine (1:1)
Procaptan
Unii-1964X464oj
Coversyl
(2S,3aS,7aS)-1-[(2S)-2-{[(1S)-1-(Ethoxycarbonyl)butyl]amino}propanoyl]octahydro-1H-indol-2-carbonsäure--2-methylpropan-2-amin(1:1)
(2S-(1(R*(R*)),2a,3ab,7ab))-1-(2-((1-(Ethoxycarbonyl)butyl)amino)-1-oxopropyl)octahydro-1H-indole-2-carboxylic Acid compd. with 2-Methyl-2-propanamine (1:1)
Perinodopril
Coversum
(2S,3aS,7aS)-1-[(2S)-2-{[(1S)-1-(ethoxycarbonyl)butyl]amino}propanoyl]octahydro-1H-indole-2-carboxylic acid - 2-methylpropan-2-amine (1:1)
Perindopril t-Butylamine
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