(Z)-13-Octadecenoic acid (BioDeep_00000022640)

   

human metabolite Endogenous


代谢物信息卡片


13-Octadecenoic acid, sodium salt, (Z)-isomer

化学式: C18H34O2 (282.2558664)
中文名称:
谱图信息: 最多检出来源 Bos taurus(endogenous) 88.89%

分子结构信息

SMILES: CCCCC=CCCCCCCCCCCCC(=O)O
InChI: InChI=1S/C18H34O2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18(19)20/h5-6H,2-4,7-17H2,1H3,(H,19,20)/b6-5-

描述信息

(Z)-13-Octadecenoic acid is a member of the class of compounds known as long-chain fatty acids. Long-chain fatty acids are fatty acids with an aliphatic tail that contains between 13 and 21 carbon atoms. (Z)-13-octadecenoic acid is practically insoluble (in water) and a weakly acidic compound (based on its pKa). Within the cell, (Z)-13-octadecenoic acid is primarily located in the membrane (predicted from logP). It can also be found in the extracellular space. (Z)-13-Octadecenoic acid is a constituent of various lipid fractions from fish and some cooked foods.

同义名列表

11 个代谢物同义名

13-Octadecenoic acid, sodium salt, (Z)-isomer; 13-Octadecenoic acid, (e)-isomer; (13Z)-octadec-13-enoic acid; (13Z)-13-Octadecenoic acid; cis-13-Octadecenoic acid; (Z)-13-Octadecenoic acid; octadec-13-enoic acid; (Z)-13-Octadecenoate; 13-Octadecenoic acid; (13Z)-Octadecenoate; 13Z-Octadecenoate



数据库引用编号

7 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

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

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

  • Muhammad Shoaib Khan, Muhammad Uzair, Muhammad Hanif, Mehreen Jabeen, Bashir Ahmad Chaudhary. Anti-inflammatory potential of spectroscopically analyzed trans-13-octadecenoic acid of Yucca elephantipes Regel roots: in-vitro and in-vivo analysis. Pakistan journal of pharmaceutical sciences. 2022 Nov; 35(6):1549-1556. doi: . [PMID: 36789814]
  • Tarvi Teder, William E Boeglin, Claus Schneider, Alan R Brash. A fungal catalase reacts selectively with the 13S fatty acid hydroperoxide products of the adjacent lipoxygenase gene and exhibits 13S-hydroperoxide-dependent peroxidase activity. Biochimica et biophysica acta. Molecular and cell biology of lipids. 2017 Jul; 1862(7):706-715. doi: 10.1016/j.bbalip.2017.03.011. [PMID: 28363790]
  • Dian Wang, Xingxing Wang, Jing Kong, Jiayan Wu, Minchao Lai. GC-MS-Based metabolomics discovers a shared serum metabolic characteristic among three types of epileptic seizures. Epilepsy research. 2016 10; 126(?):83-9. doi: 10.1016/j.eplepsyres.2016.07.003. [PMID: 27450370]
  • E A Emken, R O Adlof, W K Rohwedder, R M Gulley. Incorporation of deuterium-labeled trans- and cis-13-octadecenoic acids in human plasma lipids. Journal of lipid research. 1983 Jan; 24(1):34-46. doi: 10.1016/s0022-2275(20)38022-6. [PMID: 6833880]