2-hydroxyoctanoate (BioDeep_00000018612)
Secondary id: BioDeep_00000415946
human metabolite PANOMIX_OTCML-2023 Endogenous
代谢物信息卡片
化学式: C8H16O3 (160.10993860000002)
中文名称: 2-羟基辛酸
谱图信息:
最多检出来源 Viridiplantae(plant) 50%
Last reviewed on 2024-09-14.
Cite this Page
2-hydroxyoctanoate. BioDeep Database v3. PANOMIX ltd, a top metabolomics service provider from China.
https://query.biodeep.cn/s/2-hydroxyoctanoate (retrieved
2024-11-22) (BioDeep RN: BioDeep_00000018612). Licensed
under the Attribution-Noncommercial 4.0 International License (CC BY-NC 4.0).
分子结构信息
SMILES: CCCCCCC(C(=O)O)O
InChI: InChI=1S/C8H16O3/c1-2-3-4-5-6-7(9)8(10)11/h7,9H,2-6H2,1H3,(H,10,11)
描述信息
Hydroxyoctanoic acid medium chain substrate of the 2-hydroxy acid oxidases associated with the 3 distinct human 2-hydroxy acid oxidase genes, HAOX1, HAOX2, and HAOX3. (PMID: 10777549) [HMDB]
Hydroxyoctanoic acid medium chain substrate of the 2-hydroxy acid oxidases associated with the 3 distinct human 2-hydroxy acid oxidase genes, HAOX1, HAOX2, and HAOX3. (PMID: 10777549).
2-Hydroxyoctanoic acid is a medium chain acyl-CoA synthetase inhibitor with a Ki of 500 μM[1].
2-Hydroxyoctanoic acid is a medium chain acyl-CoA synthetase inhibitor with a Ki of 500 μM[1].
同义名列表
26 个代谢物同义名
alpha-Hydroxy-N-caprylic acid; alpha-Hydroxycaprylic acid; alpha-Hydroxyoctanoic acid; DL-2-Hydroxyoctanoic acid; alpha-Hydroxy-N-caprylate; DL-2-Hydroxycaprylic acid; a-Hydroxy-N-caprylic acid; a-Hydroxyoctanoic acid; alpha-Hydroxycaprylate; a-Hydroxycaprylic acid; alpha-Hydroxyoctanoate; Α-hydroxyoctanoic acid; 2-Hydroxycaprylic acid; 2-Hydroxyoctanoic acid; DL-2-Hydroxycaprylate; DL-2-Hydroxyoctanoate; a-Hydroxy-N-caprylate; Hydroxyoctanoic acid; 2-Hydroxy caprylate; a-Hydroxycaprylate; 2-Hydroxycaprylate; Α-hydroxyoctanoate; 2-Hydroxyoctanoate; a-Hydroxyoctanoate; Hydroxyoctanoate; alpha-HCA acid
数据库引用编号
10 个数据库交叉引用编号
- ChEBI: CHEBI:86543
- PubChem: 94180
- HMDB: HMDB0000711
- ChEMBL: CHEMBL4447980
- foodb: FDB022197
- chemspider: 84994
- CAS: 617-73-2
- PMhub: MS000009597
- RefMet: Hydroxyoctanoic acid
- medchemexpress: HY-W015444
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)
2 个相关的物种来源信息
- 7227 - Drosophila melanogaster: 10.1038/S41467-019-11933-Z
- 9606 - Homo sapiens: -
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
- Meryem Köse, Thanigaimalai Pillaiyar, Vigneshwaran Namasivayam, Elisabetta De Filippo, Katharina Sylvester, Trond Ulven, Ivar von Kügelgen, Christa E Müller. An Agonist Radioligand for the Proinflammatory Lipid-Activated G Protein-Coupled Receptor GPR84 Providing Structural Insights.
Journal of medicinal chemistry.
2020 03; 63(5):2391-2410. doi:
10.1021/acs.jmedchem.9b01339
. [PMID: 31721581] - Beate Teichmann, Caroline Labbé, François Lefebvre, Michael Bölker, Uwe Linne, Richard R Bélanger. Identification of a biosynthesis gene cluster for flocculosin a cellobiose lipid produced by the biocontrol agent Pseudozyma flocculosa.
Molecular microbiology.
2011 Mar; 79(6):1483-95. doi:
10.1111/j.1365-2958.2010.07533.x
. [PMID: 21255122] - Kashan Ahmed, Sorin Tunaru, Claus-Dieter Langhans, Julien Hanson, Christoph W Michalski, Stefan Kölker, Patricia M Jones, Jürgen G Okun, Stefan Offermanns. Deorphanization of GPR109B as a receptor for the beta-oxidation intermediate 3-OH-octanoic acid and its role in the regulation of lipolysis.
The Journal of biological chemistry.
2009 Aug; 284(33):21928-21933. doi:
10.1074/jbc.m109.019455
. [PMID: 19561068] - Michael S Murray, Ross P Holmes, W Todd Lowther. Active site and loop 4 movements within human glycolate oxidase: implications for substrate specificity and drug design.
Biochemistry.
2008 Feb; 47(8):2439-49. doi:
10.1021/bi701710r
. [PMID: 18215067]