Perindoprilat (BioDeep_00000014088)
Secondary id: BioDeep_00000408946
human metabolite Endogenous blood metabolite
代谢物信息卡片
化学式: C17H28N2O5 (340.1998)
中文名称: 培哚普利
谱图信息:
最多检出来源 Homo sapiens(blood) 20.69%
分子结构信息
SMILES: CCCC(C(=O)O)NC(C)C(=O)N1C2CCCCC2CC1C(=O)O
InChI: InChI=1S/C17H28N2O5/c1-3-6-12(16(21)22)18-10(2)15(20)19-13-8-5-4-7-11(13)9-14(19)17(23)24/h10-14,18H,3-9H2,1-2H3,(H,21,22)(H,23,24)/t10-,11-,12-,13-,14-/m0/s1
描述信息
Perindoprilat is a metabolite of perindopril. Perindopril, or perindopril arginine, (trade names include Coversyl and Aceon) is a long-acting ACE inhibitor. Perindopril is used to treat high blood pressure, heart failure or stable coronary artery disease. It is also available in a generic form, perindopril erbumine. (Wikipedia)
D004791 - Enzyme Inhibitors > D011480 - Protease Inhibitors > D000806 - Angiotensin-Converting Enzyme Inhibitors
C78274 - Agent Affecting Cardiovascular System > C270 - Antihypertensive Agent
C471 - Enzyme Inhibitor > C783 - Protease Inhibitor > C247 - ACE Inhibitor
D002317 - Cardiovascular Agents > D000959 - Antihypertensive Agents
同义名列表
44 个代谢物同义名
(2S,3aS,7aS)-1-[(2S)-2-{[(1S)-1-carboxybutyl]amino}propanoyl]-octahydro-1H-indole-2-carboxylic acid; (2S,3AS,7as)-1-[(2S)-2-{[(1S)-1-carboxybutyl]amino}propanoyl]octahydro-1H-indole-2-carboxylic acid; (2S,3aS,7aS)-1-[(2S)-2-{[(1S)-1-carboxybutyl]amino}propanoyl]-octahydroindole-2-carboxylic acid; (2S,3AS,7as)-1-[(2S)-2-{[(1S)-1-carboxybutyl]amino}propanoyl]octahydro-1H-indole-2-carboxylate; Perindoprilic acid; Perindoprilatum; Perindoprilato; SCHEMBL1269121; Perindoprilate; Perondropilat; Perindoprilat; S-9780; S 9780; X94; (2S,3aS,7aS)-1-(((S)-1-carboxybutyl)-L-alanyl)octahydro-1H-indole-2-carboxylic acid; (2S,3aS,7aS)-1-((2S)-2-(((1S)-1-carboxybutyl)amino)propanoyl)octahydro-1H-indole-2-carboxylic acid; (2S,3aS,7aS)-1-((S)-2-(((S)-1-carboxybutyl)amino)propanoyl)octahydro-1H-indole-2-carboxylic acid; (2S,3aS,7aS)-1-((S)-2-(((S)-1-carboxybutyl)amino)propanoyl)octahydro-1H-indole-2-carboxylicacid; (2S,3aS,7aS)-1-((S)-N-((S)-1-Carboxybutyl)alanyl)hexahydro-2-indolinecarboxylic acid; (2S,3aS,7aS)-1-[(2S)-2-[[(1S)-1-Carboxybutyl]amino]-1-oxopropyl]octahydro-1H-indole-2-carboxylic Acid; (2S,3aS,7aS)-1-[(2S)-2-[[(1S)-1-carboxybutyl]amino]propanoyl]-2,3,3a,4,5,6,7,7a-octahydroindole-2-carboxylic acid; (2S,3aS,7aS)-1-[(2S)-2-[[(1S)-1-Carboxybutyl]amino]propanoyl]octahydro-1H-indole-2-carboxylic Acid (Perindoprilat); (2s,3as,7as)-1-[(2s)-2-[[(2s)-1-hydroxy-1-oxopentan-2-yl]amino] propanoyl]-2,3,3a,4,5,6,7,7a-octahydroindole-2-carboxylic acid; (2S,3aS,7aS)-1-[(2S)-2-[[(2S)-1-hydroxy-1-oxopentan-2-yl]amino]propanoyl]-2,3,3a,4,5,6,7,7a-octahydroindole-2-carboxylic acid; (2S,3aS,7aS)-1-[(2S)-2-{[(1S)-1-carboxybutyl]amino}propanoyl]octahydro-1H-indole-2-carboxylic acid (non-preferred name); [2S-[1[R*(R*)],2alpha,3abeta,7abeta]]-1-[2-[(1-Carboxybutyl)amino]-1-oxopropyl]octahydro-1H-indole-2-carboxylic Acid; 1H-Indole-2-carboxylic acid, 1-[(2S)-2-[[(1S)-1-carboxybutyl]amino]-1-oxopropyl]octahydro-, (2S,3aS,7aS)-; 1H-Indole-2-carboxylic acid, 1-[2-[(1-carboxybutyl)amino]-1-oxopropyl]octahydro-, [2S-[1[R*(R*)],2a,3ass,7ass]]-; Perindoprilat; S 9780; Perindopril RC B;; 1H-Indole-2-carboxylic acid, octahydro-1-(2-((1-carboxybutyl)amino)-1-oxopropyl)-, (2S-(1(R*(R*)),2-alpha,3a-beta,7a-beta))-; 2UV6ZNQ92K; A1-06488; N-((2S)-1-((2S,3aS,7aS)-2-carboxyoctahydro-1H-indol-1-yl)-1-oxopropan-2-yl)-L-norvaline; N-{(2S)-1-[(2S,3aS,7aS)-2-carboxyoctahydro-1H-indol-1-yl]-1-oxopropan-2-yl}-L-norvaline; Perindopril diacid form; PERINDOPRIL DIACID FORM [MI]; PERINDOPRIL TERT-BUTYLAMINE IMPURITY B (EP IMPURITY); PERINDOPRIL TERT-BUTYLAMINE IMPURITY B [EP IMPURITY]; Perindoprilat [INN:BAN]; PERINDOPRILAT [INN]; Perindoprilate [French]; Perindoprilato [Spanish]; Perindoprilatum (Latin); Perindoprilatum [Latin]; Perondroprilat; UNII-2UV6ZNQ92K
数据库引用编号
12 个数据库交叉引用编号
- ChEBI: CHEBI:132041
- KEGG: C21517
- PubChem: 4687013
- PubChem: 72022
- HMDB: HMDB0060574
- DrugBank: DB14213
- ChEMBL: CHEMBL1201368
- CAS: 95153-31-4
- PMhub: MS000028701
- PubChem: 336445155
- PDB-CCD: X94
- MeSH: perindoprilat
分类词条
相关代谢途径
Reactome()
BioCyc()
PlantCyc()
代谢反应
1 个相关的代谢反应过程信息。
Reactome()
BioCyc()
WikiPathways()
Plant Reactome()
INOH()
PlantCyc()
COVID-19 Disease Map()
PharmGKB()
1 个相关的物种来源信息
在这里通过桑基图来展示出与当前的这个代谢物在我们的BioDeep知识库中具有相关联信息的其他代谢物。在这里进行关联的信息来源主要有:
- PubMed: 来源于PubMed文献库中的文献信息,我们通过自然语言数据挖掘得到的在同一篇文献中被同时提及的相关代谢物列表,这个列表按照代谢物同时出现的文献数量降序排序,取前10个代谢物作为相关研究中关联性很高的代谢物集合展示在桑基图中。
- NCBI Taxonomy: 通过文献数据挖掘,得到的代谢物物种来源信息关联。这个关联信息同样按照出现的次数降序排序,取前10个代谢物作为高关联度的代谢物集合展示在桑吉图上。
- Chemical Taxonomy: 在物质分类上处于同一个分类集合中的其他代谢物
- Chemical Reaction: 在化学反应过程中,存在为当前代谢物相关联的生化反应过程中的反应底物或者反应产物的关联代谢物信息。
点击图上的相关代谢物的名称,可以跳转到相关代谢物的信息页面。
| 亚细胞结构定位 | 关联基因列表 |
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文献列表
- Xin Zheng, Huitao Gao, Xinge Cui, Yanbao Zhang, Rui Chen, Yaqin Wang, Pauline Lauruol, Hongyun Wang. Simultaneous determination of indapamide, perindopril and its active metabolite perindoprilat in human plasma using UPLC-MS/MS method.
Journal of chromatography. B, Analytical technologies in the biomedical and life sciences.
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.
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Drug design, development and therapy.
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Analytical and bioanalytical chemistry.
2017 Oct; 409(26):6141-6148. doi:
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Analytical and bioanalytical chemistry.
2010 Jul; 397(6):2161-70. doi:
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Kidney international.
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Scandinavian journal of clinical and laboratory investigation.
1999 Apr; 59(2):147-52. doi:
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Pediatric research.
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Clinical and experimental pharmacology & physiology.
1998 Jul; 25(7-8):637-9. doi:
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Cardiology.
1998; 89(2):111-8. doi:
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Life sciences.
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1997 Nov; 90 Spec No 6(?):21-7. doi:
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Life sciences.
1997; 61(22):2157-65. doi:
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Journal of molecular and cellular cardiology.
1996 Sep; 28(9):1985-94. doi:
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Journal of cardiovascular pharmacology.
1996 May; 27(5):657-66. doi:
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British journal of clinical pharmacology.
1995 Apr; 39(4):361-8. doi:
10.1111/j.1365-2125.1995.tb04463.x. [PMID: 7640141] - R J MacFadyen, K R Lees, J L Reid. Responses to low dose intravenous perindoprilat infusion in salt deplete/salt replete normotensive volunteers.
British journal of clinical pharmacology.
1994 Oct; 38(4):329-34. doi:
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Atherosclerosis.
1994 Mar; 106(1):29-41. doi:
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European journal of pharmacology.
1994 Feb; 266(3):201-11. doi:
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European journal of clinical pharmacology.
1994; 46(3):185-9. doi:
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American heart journal.
1993 Sep; 126(3 Pt 2):794-7. doi:
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European journal of pharmacology.
1993 Aug; 240(2-3):207-12. doi:
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Kidney international.
1993 Jul; 44(1):165-72. doi:
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The American journal of cardiology.
1993 Jun; 71(17):57E-60E. doi:
10.1016/0002-9149(93)90954-b. [PMID: 8392282] - R J MacFadyen, K R Lees, J L Reid. Double blind controlled study of low dose intravenous perindoprilat or enalaprilat infusion in elderly patients with heart failure.
British heart journal.
1993 Apr; 69(4):293-7. doi:
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International journal of clinical pharmacology, therapy, and toxicology.
1992 Sep; 30(9):325-30. doi:
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British journal of clinical pharmacology.
1992 Aug; 34(2):115-21. doi:
10.1111/j.1365-2125.1992.tb04119.x. [PMID: 1419473] - C A Muller, L H Opie, M Peisach, C A Pineda. Antiarrhythmic effects of the angiotensin converting enzyme inhibitor perindoprilat in a pig model of acute regional myocardial ischemia.
Journal of cardiovascular pharmacology.
1992 May; 19(5):748-54. doi:
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British journal of clinical pharmacology.
1992 Mar; 33(3):326-8. doi:
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British journal of clinical pharmacology.
1992 Jan; 33(1):93-9. doi:
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1991 Aug; 32(2):193-9. doi:
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1991 Aug; 32(2):187-92. doi:
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American journal of hypertension.
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Fundamental & clinical pharmacology.
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1989 Oct; 17(5):529-50. doi:
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1989 Aug; 7(8):633-8. doi:
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1989 Mar; 488(1):249-65. doi:
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1988 Dec; 6(3):S55-6. doi:
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