Linoleamide (BioDeep_00000022062)

   

human metabolite Endogenous


代谢物信息卡片


(9Z,12Z)-octadeca-9,12-dienimidic acid

化学式: C18H33NO (279.2562008)
中文名称: 亚油酰胺, 亚油酸酰胺
谱图信息: 最多检出来源 Homo sapiens(feces) 3.64%

Reviewed

Last reviewed on 2024-06-29.

Cite this Page

Linoleamide. BioDeep Database v3. PANOMIX ltd, a top metabolomics service provider from China. https://query.biodeep.cn/s/linoleamide (retrieved 2024-11-23) (BioDeep RN: BioDeep_00000022062). Licensed under the Attribution-Noncommercial 4.0 International License (CC BY-NC 4.0).

分子结构信息

SMILES: CCCCC/C=C\C/C=C\CCCCCCCC(=O)N
InChI: InChI=1S/C18H33NO/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18(19)20/h6-7,9-10H,2-5,8,11-17H2,1H3,(H2,19,20)/b7-6-,10-9-

描述信息

Linoleamide, also known as 9,12-Octadecadienamide or Linoleic acid amide, is classified as a member of the Fatty amides. Fatty amides are carboxylic acid amide derivatives of fatty acids, that are formed from a fatty acid and an amine. Linoleamide is considered to be practically insoluble (in water) and relatively neutral. Linoleamide is a fatty amide lipid molecule

同义名列表

8 个代谢物同义名

(9Z,12Z)-octadeca-9,12-dienimidic acid; (9Z,12Z)-octadeca-9,12-dien-1-amide; octadeca-9,12-dienamide; 9,12-Octadecadienamide; Linoleic acid amide; Linoleate amide; Linoleoyl amide; linoleamide



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)

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。



文献列表

  • Nalin Singh, Bogdan Barnych, Christophe Morisseau, Karen M Wagner, Debin Wan, Ashley Takeshita, Hoang Pham, Ting Xu, Abhaya Dandekar, Jun-Yan Liu, Bruce D Hammock. N-Benzyl-linoleamide, a Constituent of Lepidium meyenii (Maca), Is an Orally Bioavailable Soluble Epoxide Hydrolase Inhibitor That Alleviates Inflammatory Pain. Journal of natural products. 2020 12; 83(12):3689-3697. doi: 10.1021/acs.jnatprod.0c00938. [PMID: 33320645]
  • Edyta Adamska-Patruno, Joanna Godzien, Michal Ciborowski, Paulina Samczuk, Witold Bauer, Katarzyna Siewko, Maria Gorska, Coral Barbas, Adam Kretowski. The Type 2 Diabetes Susceptibility PROX1 Gene Variants Are Associated with Postprandial Plasma Metabolites Profile in Non-Diabetic Men. Nutrients. 2019 Apr; 11(4):. doi: 10.3390/nu11040882. [PMID: 31010169]
  • Kuljeet S Gugnani, Nguyen Vu, Alejandro N Rondón-Ortiz, Mark Böhlke, Timothy J Maher, Alejandro J Pino-Figueroa. Neuroprotective activity of macamides on manganese-induced mitochondrial disruption in U-87 MG glioblastoma cells. Toxicology and applied pharmacology. 2018 02; 340(?):67-76. doi: 10.1016/j.taap.2017.12.014. [PMID: 29288688]
  • Jaroslaw Piszcz, Emily G Armitage, Alessia Ferrarini, Francisco J Rupérez, Agnieszka Kulczynska, Lukasz Bolkun, Janusz Kloczko, Adam Kretowski, Alina Urbanowicz, Michal Ciborowski, Coral Barbas. To treat or not to treat: metabolomics reveals biomarkers for treatment indication in chronic lymphocytic leukaemia patients. Oncotarget. 2016 Apr; 7(16):22324-38. doi: 10.18632/oncotarget.8078. [PMID: 26988915]
  • Tianxun Gong, Nan Zhang, Kien Voon Kong, Douglas Goh, Cui Ying, Jean-Louis Auguste, Perry Ping Shum, Lei Wei, Georges Humbert, Ken-Tye Yong, Malini Olivo. Rapid SERS monitoring of lipid-peroxidation-derived protein modifications in cells using photonic crystal fiber sensor. Journal of biophotonics. 2016 Jan; 9(1-2):32-7. doi: 10.1002/jbio.201500168. [PMID: 26366883]
  • Haifa Almukadi, Hui Wu, Mark Böhlke, Charles J Kelley, Timothy J Maher, Alejandro Pino-Figueroa. The macamide N-3-methoxybenzyl-linoleamide is a time-dependent fatty acid amide hydrolase (FAAH) inhibitor. Molecular neurobiology. 2013 Oct; 48(2):333-9. doi: 10.1007/s12035-013-8499-2. [PMID: 23853040]
  • Emma K Farrell, Yuden Chen, Muna Barazanji, Kristen A Jeffries, Felipe Cameroamortegui, David J Merkler. Primary fatty acid amide metabolism: conversion of fatty acids and an ethanolamine in N18TG2 and SCP cells. Journal of lipid research. 2012 Feb; 53(2):247-56. doi: 10.1194/jlr.m018606. [PMID: 22095832]
  • Tran Thi Hong Hanh, Dan Thi Thuy Hang, Chau Van Minh, Nguyen Tien Dat. Anti-inflammatory effects of fatty acids isolated from Chromolaena odorata. Asian Pacific journal of tropical medicine. 2011 Oct; 4(10):760-3. doi: 10.1016/s1995-7645(11)60189-2. [PMID: 22014728]
  • Xiaohui Yuan, Tuong Chi Ta, Min Lin, Jane R Evans, Yinchen Dong, Eugene Bolotin, Mark A Sherman, Barry M Forman, Frances M Sladek. Identification of an endogenous ligand bound to a native orphan nuclear receptor. PloS one. 2009; 4(5):e5609. doi: 10.1371/journal.pone.0005609. [PMID: 19440305]
  • T C Jenkins, C S Adams. The biohydrogenation of linoleamide in vitro and its effects on linoleic acid concentration in duodenal contents of sheep. Journal of animal science. 2002 Feb; 80(2):533-40. doi: 10.2527/2002.802533x. [PMID: 11881938]
  • J K Huang, C R Jan. Linoleamide, a brain lipid that induces sleep, increases cytosolic Ca2+ levels in MDCK renal tubular cells. Life sciences. 2001 Jan; 68(9):997-1004. doi: 10.1016/s0024-3205(00)01002-x. [PMID: 11212875]
  • R B Markham, P W Stashak, B Prescott, D F Amsbaugh, P J Baker. Effect of concanavalin A on lymphocyte interactions involved in the antibody response to type III pneumococcal polysaccharide I. Comparison of the suppression induced by con A and low dose paralysis. Journal of immunology (Baltimore, Md. : 1950). 1977 Mar; 118(3):952-6. doi: NULL. [PMID: 15032]