9,10-Epoxystearate (BioDeep_00000897623)

 

Secondary id: BioDeep_00001892036


代谢物信息卡片


9,10-Epoxystearate

化学式: C18H33O3- (297.2429568)
中文名称:
谱图信息: 最多检出来源 Viridiplantae(plant) 32.35%

分子结构信息

SMILES: CCCCCCCCC1C(O1)CCCCCCCC(=O)[O-]
InChI: InChI=1S/C18H34O3/c1-2-3-4-5-7-10-13-16-17(21-16)14-11-8-6-9-12-15-18(19)20/h16-17H,2-15H2,1H3,(H,19,20)/p-1

描述信息

同义名列表

1 个代谢物同义名

9,10-Epoxystearate



数据库引用编号

2 个数据库交叉引用编号

分类词条

相关代谢途径

Reactome(0)

BioCyc(0)

PlantCyc(0)

代谢反应

4 个相关的代谢反应过程信息。

Reactome(0)

BioCyc(0)

WikiPathways(0)

Plant Reactome(0)

INOH(0)

PlantCyc(4)

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

  • Kelsey Hildreth, Sean D Kodani, Bruce D Hammock, Ling Zhao. Cytochrome P450-derived linoleic acid metabolites EpOMEs and DiHOMEs: a review of recent studies. The Journal of nutritional biochemistry. 2020 12; 86(?):108484. doi: 10.1016/j.jnutbio.2020.108484. [PMID: 32827665]
  • Ying Liu, Jinwei Li, Yuanfa Liu. Effects of epoxy stearic acid on lipid metabolism in HepG2 cells. Journal of food science. 2020 Oct; 85(10):3644-3652. doi: 10.1111/1750-3841.15405. [PMID: 32885409]
  • Martina Decker, Magdalena Adamska, Annette Cronin, Francesca Di Giallonardo, Julia Burgener, Anne Marowsky, John R Falck, Christophe Morisseau, Bruce D Hammock, Artiom Gruzdev, Darryl C Zeldin, Michael Arand. EH3 (ABHD9): the first member of a new epoxide hydrolase family with high activity for fatty acid epoxides. Journal of lipid research. 2012 Oct; 53(10):2038-2045. doi: 10.1194/jlr.m024448. [PMID: 22798687]
  • Sylvie Kandel, Marc Morant, Irène Benveniste, Elizabeth Blée, Danièle Werck-Reichhart, Franck Pinot. Cloning, functional expression, and characterization of CYP709C1, the first sub-terminal hydroxylase of long chain fatty acid in plants. Induction by chemicals and methyl jasmonate. The Journal of biological chemistry. 2005 Oct; 280(43):35881-9. doi: 10.1074/jbc.m500918200. [PMID: 16120613]
  • Valérie Le Quéré, Emmanuelle Plée-Gautier, Philippe Potin, Stéphanie Madec, Jean-Pierre Salaün. Human CYP4F3s are the main catalysts in the oxidation of fatty acid epoxides. Journal of lipid research. 2004 Aug; 45(8):1446-58. doi: 10.1194/jlr.m300463-jlr200. [PMID: 15145985]
  • Dimitrios Tsikas, Anja Mitschke, Frank-Mathias Gutzki, Hartmut H Meyer, Jürgen C Frölich. Gas chromatography-mass spectrometry of cis-9,10-epoxyoctadecanoic acid (cis-EODA). II. Quantitative determination of cis-EODA in human plasma. Journal of chromatography. B, Analytical technologies in the biomedical and life sciences. 2004 May; 804(2):403-12. doi: 10.1016/j.jchromb.2004.01.055. [PMID: 15081936]
  • Stephan Summerer, Abdulsamie Hanano, Shigeru Utsumi, Michael Arand, Francis Schuber, Elizabeth Blée. Stereochemical features of the hydrolysis of 9,10-epoxystearic acid catalysed by plant and mammalian epoxide hydrolases. The Biochemical journal. 2002 Sep; 366(Pt 2):471-80. doi: 10.1042/bj20011778. [PMID: 12020347]
  • F Pinot, I Benveniste, J P Salaün, O Loreau, J P Noël, L Schreiber, F Durst. Production in vitro by the cytochrome P450 CYP94A1 of major C18 cutin monomers and potential messengers in plant-pathogen interactions: enantioselectivity studies. The Biochemical journal. 1999 Aug; 342 ( Pt 1)(?):27-32. doi: 10.1042/0264-6021:3420027. [PMID: 10432296]
  • E S Kaneshiro. Lipid metabolism of Pneumocystis: toward the definition of new molecular targets. FEMS immunology and medical microbiology. 1998 Sep; 22(1-2):135-43. doi: 10.1111/j.1574-695x.1998.tb01198.x. [PMID: 9792072]
  • V Spitzer, W Tomberg, R Hartmann, R Aichholz. Analysis of the seed oil of Heisteria silvanii (Olacaceae)--a rich source of a novel C18 acetylenic fatty acid. Lipids. 1997 Nov; 32(11):1189-200. doi: 10.1007/s11745-997-0153-6. [PMID: 9397405]
  • G A Ulsaker, G Teien. Identification of 9,10-epoxyoctadecanoic acid in human urine using gas chromatography-mass spectrometry. Biomedical chromatography : BMC. 1995 Jul; 9(4):183-7. doi: 10.1002/bmc.1130090407. [PMID: 8520208]
  • E Blée, F Schuber. Regio- and enantioselectivity of soybean fatty acid epoxide hydrolase. The Journal of biological chemistry. 1992 Jun; 267(17):11881-7. doi: . [PMID: 1601858]
  • R Sharma, S Gupta, S S Singhal, G A Ansari, Y C Awasthi. Glutathione S-transferase-catalyzed conjugation of 9,10-epoxystearic acid with glutathione. Journal of biochemical toxicology. 1991; 6(2):147-53. doi: 10.1002/jbt.2570060209. [PMID: 1941901]
  • A P TULLOCH, B M CRAIG, G A LEDINGHAM. The oil of wheat stem rust uredospores. II. The isolation of cis-9,10-epoxyoctadecanoic acid, and the fatty acid composition of the oil. Canadian journal of microbiology. 1959 Oct; 5(?):485-91. doi: 10.1139/m59-060. [PMID: 13839791]