CAR 4:0 (BioDeep_00000630421)
代谢物信息卡片
化学式: C11H21NO4 (231.1470506)
中文名称:
谱图信息:
最多检出来源 () 0%
分子结构信息
SMILES: CC(C)C(=O)OC(CC(=O)[O-])C[N+](C)(C)C
InChI: InChI=1S/C11H21NO4/c1-5-6-11(15)16-9(7-10(13)14)8-12(2,3)4/h9H,5-8H2,1-4H3
数据库引用编号
8 个数据库交叉引用编号
- ChEBI: CHEBI:73017
- PubChem: 10177002
- LipidMAPS: LMFA07070075
- LipidMAPS: LMFA07070054
- LipidMAPS: LMFA07070003
- CAS: 25518-50-7
- CAS: 25518-48-3
- RefMet: CAR 4:0
分类词条
相关代谢途径
Reactome(0)
BioCyc(0)
PlantCyc(0)
代谢反应
0 个相关的代谢反应过程信息。
Reactome(0)
BioCyc(0)
WikiPathways(0)
Plant Reactome(0)
INOH(0)
PlantCyc(0)
COVID-19 Disease Map(0)
PathBank(0)
PharmGKB(0)
0 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。
文献列表
- Masashi Ikuno, Hodaka Yamakado, Ikuko Amano, Yusuke Hatanaka, Norihito Uemura, Shu-Ichi Matsuzawa, Ryosuke Takahashi. Mitochondrial dysfunction in a mouse model of prodromal Parkinson's disease: A metabolomic analysis.
Neuroscience letters.
2021 11; 765(?):136267. doi:
10.1016/j.neulet.2021.136267
. [PMID: 34571089] - Lina Luo, Ragu Ramanathan, Lauren Horlbogen, Sumathy Mathialagan, Chester Costales, Manoli Vourvahis, Christopher L Holliman, A David Rodrigues. A Multiplexed HILIC-MS/HRMS Assay for the Assessment of Transporter Inhibition Biomarkers in Phase I Clinical Trials: Isobutyryl-Carnitine as an Organic Cation Transporter (OCT1) Biomarker.
Analytical chemistry.
2020 07; 92(14):9745-9754. doi:
10.1021/acs.analchem.0c01144
. [PMID: 32551505] - Sabrina Forni, Xiaowei Fu, Susan E Palmer, Lawrence Sweetman. Rapid determination of C4-acylcarnitine and C5-acylcarnitine isomers in plasma and dried blood spots by UPLC-MS/MS as a second tier test following flow-injection MS/MS acylcarnitine profile analysis.
Molecular genetics and metabolism.
2010 Sep; 101(1):25-32. doi:
10.1016/j.ymgme.2010.05.012
. [PMID: 20591710] - B Merinero, C Pérez-Cerdá, P Ruiz Sala, I Ferrer, M J García, M Martínez Pardo, A Belanger-Quintana, J L de la Mota, E Martin-Hernández, C Vianey-Saban, C Bischoff, N Gregersen, M Ugarte. Persistent increase of plasma butyryl/isobutyrylcarnitine concentrations as marker of SCAD defect and ethylmalonic encephalopathy.
Journal of inherited metabolic disease.
2006 Oct; 29(5):685. doi:
10.1007/s10545-006-0342-8
. [PMID: 16906473] - Dwight D Koeberl, Sarah P Young, Niels S Gregersen, Jerry Vockley, Wendy E Smith, Daniel Kelly Benjamin, Yan An, Susan D Weavil, Shu H Chaing, Deeksha Bali, Marie T McDonald, Priya S Kishnani, Y-T Chen, David S Millington. Rare disorders of metabolism with elevated butyryl- and isobutyryl-carnitine detected by tandem mass spectrometry newborn screening.
Pediatric research.
2003 Aug; 54(2):219-23. doi:
10.1203/01.pdr.0000074972.36356.89
. [PMID: 12736383] - C R Roe, S D Cederbaum, D S Roe, R Mardach, A Galindo, L Sweetman. Isolated isobutyryl-CoA dehydrogenase deficiency: an unrecognized defect in human valine metabolism.
Molecular genetics and metabolism.
1998 Dec; 65(4):264-71. doi:
10.1006/mgme.1998.2758
. [PMID: 9889013] - T Sakuma, N Sugiyama, T Ichiki, M Kobayashi, Y Wada, D Nohara. Analysis of acylcarnitines in maternal urine for prenatal diagnosis of glutaric aciduria type 2.
Prenatal diagnosis.
1991 Feb; 11(2):77-82. doi:
10.1002/pd.1970110203
. [PMID: 2062823]