MG(0:0/16:0/0:0) (BioDeep_00000018499)

 

Secondary id: BioDeep_00000406192, BioDeep_00000864099

human metabolite PANOMIX_OTCML-2023 Endogenous blood metabolite LipidSearch Volatile Flavor Compounds


代谢物信息卡片


1,3-Dihydroxypropan-2-yl palmitic acid

化学式: C19H38O4 (330.2769948)
中文名称: 2-单棕榈酸甘油, 2-棕榈酰-rac-甘油
谱图信息: 最多检出来源 Homo sapiens(feces) 3.3%

Reviewed

Last reviewed on 2024-10-24.

Cite this Page

MG(0:0/16:0/0:0). BioDeep Database v3. PANOMIX ltd, a top metabolomics service provider from China. https://query.biodeep.cn/s/mg(0:0_16:0_0:0) (retrieved 2024-11-22) (BioDeep RN: BioDeep_00000018499). Licensed under the Attribution-Noncommercial 4.0 International License (CC BY-NC 4.0).

分子结构信息

SMILES: CCCCCCCCCCCCCCCC(=O)OC(CO)CO
InChI: InChI=1S/C19H38O4/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-19(22)23-18(16-20)17-21/h18,20-21H,2-17H2,1H3

描述信息

MG(0:0/16:0/0:0) is a monoacylglyceride. A monoglyceride, more correctly known as a monoacylglycerol, is a glyceride consisting of one fatty acid chain covalently bonded to a glycerol molecule through an ester linkage. Monoacylglycerol can be broadly divided into two groups; 1-monoacylglycerols (or 3-monoacylglycerols) and 2-monoacylglycerols, depending on the position of the ester bond on the glycerol moiety. Normally the 1-/3-isomers are not distinguished from each other and are termed alpha-monoacylglycerols, while the 2-isomers are beta-monoacylglycerols. Monoacylglycerols are formed biochemically via release of a fatty acid from diacylglycerol by diacylglycerol lipase or hormone sensitive lipase. Monoacylglycerols are broken down by monoacylglycerol lipase. They tend to be minor components only of most plant and animal tissues, and indeed would not be expected to accumulate because their strong detergent properties would have a disruptive effect on membranes. 2-Monoacylglycerols are a major end product of the intestinal digestion of dietary fats in animals via the enzyme pancreatic lipase. They are taken up directly by the intestinal cells and converted to triacylglycerols via the monoacylglycerol pathway before being transported in lymph to the liver. Mono- and Diglycerides are commonly added to commercial food products in small quantities. They act as emulsifiers, helping to mix ingredients such as oil and water that would not otherwise blend well.
Minor component of olive oil and other vegetable oils
2-Palmitoylglycerol (2-Palm-Gl), an congener of 2-arachidonoylglycerol (2-AG), is a modest cannabinoid receptor CB1 agonist. 2-Palmitoylglycerol also may be an endogenous ligand for GPR119[1].
2-Palmitoylglycerol (2-Palm-Gl), an congener of 2-arachidonoylglycerol (2-AG), is a modest cannabinoid receptor CB1 agonist. 2-Palmitoylglycerol also may be an endogenous ligand for GPR119[1].

同义名列表

23 个代谢物同义名

1,3-Dihydroxypropan-2-yl palmitic acid; 1,3-dihydroxypropan-2-yl hexadecanoate; 1,3-Dihydroxypropan-2-yl palmitate; 2-Hexadecanoyl-rac-glycerol; Glycerol 2-hexadecanoate; 2-Monopalmitoylglycerol; 2-Hexadecanoylglycerol; 2-O-Palmitoylglycerol; beta-Monoacylglycerol; 2-palmitoyl-glycerol; 1-Monoacylglyceride; 2-Palmitoylglycerol; b-Monoacylglycerol; 1-Monoacylglycerol; MG (0:0/16:0/0:0); MG(0:0/16:0/0:0); 2-Monopalmitin; MAG(0:0/16:0); MG(0:0/16:0); 2-Palm-GL; MAG(16:0); MG(16:0); 2-Palmitoyl-rac-glycerol



数据库引用编号

9 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

157 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(157)

PharmGKB(0)

7 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

  • Teng Wei, Abdul Mueed, Ting Luo, Yong Sun, Bing Zhang, Liufeng Zheng, Zeyuan Deng, Jing Li. 1,3-Dioleoyl-2-palmitoyl-glycerol and 1-oleoyl-2-palmitoyl-3-linoleoyl-glycerol: Structure-function relationship, triacylglycerols preparation, nutrition value. Food chemistry. 2024 Jun; 443(?):138560. doi: 10.1016/j.foodchem.2024.138560. [PMID: 38295563]
  • Teng Wei, Yanping Wu, Yong Sun, Zeyuan Deng, Jing Li. Human milk phospholipid analog improved the digestion and absorption of 1,3-dioleoyl-2-palmitoyl-glycerol. Food & function. 2023 Jul; 14(13):6106-6114. doi: 10.1039/d2fo03759a. [PMID: 37326107]
  • Mohammad Bashashati, Emma Leishman, Heather Bradshaw, Solmaz Sigaroodi, Eric Tatro, Tamis Bright, Richard McCallum, Irene Sarosiek. Plasma endocannabinoids and cannabimimetic fatty acid derivatives are altered in gastroparesis: A sex- and subtype-dependent observation. Neurogastroenterology and motility : the official journal of the European Gastrointestinal Motility Society. 2021 01; 33(1):e13961. doi: 10.1111/nmo.13961. [PMID: 32779297]
  • Brian D Piccolo, James L Graham, Kimber L Stanhope, Oliver Fiehn, Peter J Havel, Sean H Adams. Plasma amino acid and metabolite signatures tracking diabetes progression in the UCD-T2DM rat model. American journal of physiology. Endocrinology and metabolism. 2016 06; 310(11):E958-69. doi: 10.1152/ajpendo.00052.2016. [PMID: 27094034]
  • S Sharmila, I Christiana, P Kiran, M V R Reddy, K Sankaran, P Kaliraj. Bacterial lipid modification enhances immunoprophylaxis of filarial abundant larval transcript-2 protein in Mastomys model. Parasite immunology. 2013 Jul; 35(7-8):201-13. doi: 10.1111/pim.12034. [PMID: 23495791]
  • J Bruce German, Robert A Gibson, Ronald M Krauss, Paul Nestel, Benoît Lamarche, Wija A van Staveren, Jan M Steijns, Lisette C P G M de Groot, Adam L Lock, Frédéric Destaillats. A reappraisal of the impact of dairy foods and milk fat on cardiovascular disease risk. European journal of nutrition. 2009 Jun; 48(4):191-203. doi: 10.1007/s00394-009-0002-5. [PMID: 19259609]
  • Wakako Tsuzuki. Absorption properties of micellar lipid metabolites into Caco2 cells. Lipids. 2007 Jul; 42(7):613-9. doi: 10.1007/s11745-007-3076-y. [PMID: 17582542]
  • Tomoko Konishi, Hideo Satsu, Yasuo Hatsugai, Koichi Aizawa, Takahiro Inakuma, Shinji Nagata, Sho-Hei Sakuda, Hiromichi Nagasawa, Makoto Shimizu. Inhibitory effect of a bitter melon extract on the P-glycoprotein activity in intestinal Caco-2 cells. British journal of pharmacology. 2004 Oct; 143(3):379-87. doi: 10.1038/sj.bjp.0705804. [PMID: 15351776]