12,13-EpOME (BioDeep_00000014529)

Main id: BioDeep_00000003295

 

human metabolite Endogenous blood metabolite


代谢物信息卡片


(9Z)-11-(3-Pentyloxiran-2-yl)undec-9-enoic acids

化学式: C18H32O3 (296.2351)
中文名称:
谱图信息: 最多检出来源 () 0%

分子结构信息

SMILES: C(CCCCCCC/C=C\CC1OC1CCCCC)(=O)O
InChI: InChI=1S/C18H32O3/c1-2-3-10-13-16-17(21-16)14-11-8-6-4-5-7-9-12-15-18(19)20/h8,11,16-17H,2-7,9-10,12-15H2,1H3,(H,19,20)

描述信息

12,13-EpOME is the 12,13-cis epoxide of linoleic acid, generated by neutrophils during the oxidative burst. The toxicity and biosynthesis of 12,13-EpOME has not been well differentiated from 9,10-EpOME, but has been presumed to be essentially the same.P [HMDB]. Vernolic acid is found in rice.
12,13-EpOME is the 12,13-cis epoxide of linoleic acid, generated by neutrophils during the oxidative burst. The toxicity and biosynthesis of 12,13-EpOME has not been well differentiated from 9,10-EpOME, but has been presumed to be essentially the same.P.

同义名列表

36 个代谢物同义名

(9Z)-11-(3-Pentyloxiran-2-yl)undec-9-enoic acids; (9Z)-11-(3-Pentyloxiran-2-yl)undec-9-enoic acid; (12R,13S)-(9Z)-12,13-Epoxyoctadecenoic acid; (9Z)-11-(3-Pentyloxiran-2-yl)undec-9-enoate; (+/-)-12(13)-epoxy-9Z-octadecenoic acid; 12,13-Monoepoxy-cis-9-octadecenoic acid; cis-12-Epoxyoctadeca-cis-9-enoic acid; cis-12,13-Epoxy-9-octadecenoic acid; (+/-)-12(13)-epoxy-9Z-octadecenoate; 12,13-Epoxy-cis-9-octadecenoic acid; 12,13-Monoepoxy-cis-9-octadecenoate; 12,13-Epoxy-9(Z)-octadecenoic acid; 12,13-Epoxyoctadec-9(Z)-enoic acid; cis-12-Epoxyoctadeca-cis-9-enoate; (9Z)-12,13-Epoxyoctadecenoic acid; 12,13-cis-Epoxyoctadecenoic acid; 12,13-epoxy-9-octadecenoic acid; 12,13-Epoxy-cis-9-octadecenoate; cis-12,13-Epoxy-9-octadecenoate; 12,13-Epoxyoctadec-9(Z)-enoate; 12,13-Epoxy-9(Z)-octadecenoate; (9Z)-12,13-Epoxyoctadecenoate; 12,13-cis-Epoxyoctadecenoate; cis-12,13-Ep, 9C-18:1; Acide vernolique; Vernolic acids; Vernolsaeuren; isoleukotoxin; Vernolic acid; 12(13)-EpOME; Vernolsaeure; 12,13-EpOME; Vernoleate; VERNOLATE; 12,13-EOA; FA 18:2;O



数据库引用编号

16 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

2 个相关的代谢反应过程信息。

Reactome(0)

BioCyc(0)

WikiPathways(2)

Plant Reactome(0)

INOH(0)

PlantCyc(0)

COVID-19 Disease Map(0)

PathBank(0)

PharmGKB(0)

3 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


文献列表

  • Dorottya Nagy-Szakal, Dinesh K Barupal, Bohyun Lee, Xiaoyu Che, Brent L Williams, Ellie J R Kahn, Joy E Ukaigwe, Lucinda Bateman, Nancy G Klimas, Anthony L Komaroff, Susan Levine, Jose G Montoya, Daniel L Peterson, Bruce Levin, Mady Hornig, Oliver Fiehn, W Ian Lipkin. Insights into myalgic encephalomyelitis/chronic fatigue syndrome phenotypes through comprehensive metabolomics. Scientific reports. 2018 07; 8(1):10056. doi: 10.1038/s41598-018-28477-9. [PMID: 29968805]
  • Todd R Harris, Pavel A Aronov, Paul D Jones, Hiromasa Tanaka, Michael Arand, Bruce D Hammock. Identification of two epoxide hydrolases in Caenorhabditis elegans that metabolize mammalian lipid signaling molecules. Archives of biochemistry and biophysics. 2008 Apr; 472(2):139-49. doi: 10.1016/j.abb.2008.01.016. [PMID: 18267101]
  • Joomi Ha, Maxim Dobretsov, Richard C Kurten, David F Grant, Joseph R Stimers. Effect of linoleic acid metabolites on Na(+)/K(+) pump current in N20.1 oligodendrocytes: role of membrane fluidity. Toxicology and applied pharmacology. 2002 Jul; 182(1):76-83. doi: 10.1006/taap.2002.9435. [PMID: 12127265]
  • S Singh, S Thomaeus, M Lee, A Green, S Stymne. Inhibition of polyunsaturated fatty acid accumulation in plants expressing a fatty acid epoxygenase. Biochemical Society transactions. 2000 Dec; 28(6):940-2. doi: 10.1042/bst0280940. [PMID: 11171264]
  • K W Cho, R L Malvin. Renin inactivation during in vitro experiments. The American journal of physiology. 1979 May; 236(5):F501-4. doi: 10.1152/ajprenal.1979.236.5.f501. [PMID: 443387]