PE 34:1 (BioDeep_00000410772)

Main id: BioDeep_00000004081

 

LipidSearch


代谢物信息卡片


7-Octadecenoic acid, 1-[[[(2-aminoethoxy)hydroxyphosphinyl]oxy]methyl]-2-[(1-oxohexadecyl)oxy]ethyl ester, [R-(Z)]- (9CI)

化学式: C39H76NO8P (717.5308)
中文名称:
谱图信息: 最多检出来源 Homo sapiens(lipidomics) 38.28%

分子结构信息

SMILES: CCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCC=CCCCCCCCCCC)COP(=O)(O)OCCN
InChI: InChI=1S/C39H76NO8P/c1-3-5-7-9-11-13-15-16-17-18-19-20-22-23-25-27-29-31-38(41)45-35-37(36-47-49(43,44)46-34-33-40)48-39(42)32-30-28-26-24-21-14-12-10-8-6-4-2/h10,12,37H,3-9,11,13-36,40H2,1-2H3,(H,43,44)/b12-10-/t37-/m1/s1

描述信息

Found in mouse brain; TwoDicalId=80; MgfFile=160720_brain_AA_18_Neg; MgfId=1248

同义名列表

51 个代谢物同义名

1-hexadecanoyl-2-(9Z-octadecenoyl)-sn-glycero-3-phosphoethanolamine; 1-Palmitoyl-2-oleoyl-sn-glycero-3-phosphoethanolamine; PE(16:0/18:1(9Z)); PE(16:0/18:1); PE(16:0_18:1); PE(34:1); PE 34:1; 1-octadecanoyl-2-(9Z-hexadecenoyl)-glycero-3-phosphoethanolamine; PE(18:0/16:1(9Z)); PE(16:1_18:0); 1-(11Z-docosenoyl)-2-dodecanoyl-glycero-3-phosphoethanolamine; PE(22:1(11Z)/12:0); PE(12:0_22:1); 1-(11Z-eicosenoyl)-2-tetradecanoyl-glycero-3-phosphoethanolamine; PE(20:1(11Z)/14:0); PE(14:0_20:1); 1-eicosanoyl-2-(9Z-tetradecenoyl)-glycero-3-phosphoethanolamine; PE(20:0/14:1(9Z)); PE(14:1_20:0); 1-(9Z-nonadecenoyl)-2-pentadecanoyl-glycero-3-phosphoethanolamine; PE(19:1(9Z)/15:0); PE(15:0_19:1); 1-nonadecanoyl-2-(9Z-pentadecenoyl)-glycero-3-phosphoethanolamine; PE(19:0/15:1(9Z)); PE(15:1_19:0); 1-(9Z-heptadecenoyl)-2-heptadecanoyl-glycero-3-phosphoethanolamine; PE(17:1(9Z)/17:0); PE(17:0_17:1); 1-heptadecanoyl-2-(9Z-heptadecenoyl)-glycero-3-phosphoethanolamine; PE(17:0/17:1(9Z)); 1-(9Z-hexadecenoyl)-2-octadecanoyl-glycero-3-phosphoethanolamine; PE(16:1(9Z)/18:0); 1-(9Z-pentadecenoyl)-2-nonadecanoyl-glycero-3-phosphoethanolamine; PE(15:1(9Z)/19:0); 1-pentadecanoyl-2-(9Z-nonadecenoyl)-glycero-3-phosphoethanolamine; PE(15:0/19:1(9Z)); 1-(9Z-tetradecenoyl)-2-eicosanoyl-glycero-3-phosphoethanolamine; PE(14:1(9Z)/20:0); 1-tetradecanoyl-2-(11Z-eicosenoyl)-glycero-3-phosphoethanolamine; PE(14:0/20:1(11Z)); 1-dodecanoyl-2-(11Z-docosenoyl)-glycero-3-phosphoethanolamine; PE(12:0/22:1(11Z)); 7-Octadecenoic acid, 1-[[[(2-aminoethoxy)hydroxyphosphinyl]oxy]methyl]-2-[(1-oxohexadecyl)oxy]ethyl ester, [R-(Z)]- (9CI); 1-hexadecanoyl-2-(7Z-octadecenoyl)-sn-glycero-3-phosphoethanolamine; PE(16:0/18:1(7Z)); 9-Octadecenoic acid (Z)-, 3-[[(2-aminoethoxy)hydroxyphosphinyl]oxy]-2-[(1-oxohexadecyl)oxy]propyl ester, (R)-; 1-(9Z-octadecenoyl)-2-hexadecanoyl-sn-glycero-3-phosphoethanolamine; PE(18:1(9Z)/16:0); PE(18:1/16:0); 1-hexadecanoyl-2-(11Z-octadecenoyl)-sn-glycero-3-phosphoethanolamine; PE(16:0/18:1(11Z))



数据库引用编号

64 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

34 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(34)

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。

亚细胞结构定位 关联基因列表
Cytoplasm 5 BLCAP, HTT, PEF1, TCIM, TXNIP
Golgi apparatus, trans-Golgi network membrane 1 AQP2
Peripheral membrane protein 2 HK1, PEF1
Endosome membrane 1 HTT
Endoplasmic reticulum membrane 2 SFTPA1, SFTPD
Nucleus 3 BLCAP, HTT, TCIM
autophagosome 1 HTT
cytosol 6 APOA1, HK1, HTT, PFKFB2, TCIM, TXNIP
dendrite 2 HTT, OPRM1
nucleoplasm 4 CD2, HTT, PFKFB2, TCIM
Cell membrane 5 AQP2, CD2, HTR3A, HTT, OPRM1
Cleavage furrow 1 HTR3A
Cell projection, axon 1 OPRM1
Multi-pass membrane protein 6 AQP2, BLCAP, HTR3A, HTT, OPRM1, TPRA1
Synapse 3 HTR3A, HTT, OPRM1
cell surface 1 CD2
Golgi apparatus 5 AQP2, CD2, HTT, OCIAD1, OPRM1
Golgi membrane 1 INS
postsynapse 1 HTR3A
presynaptic membrane 1 HTT
Cytoplasm, cytosol 1 HK1
Lysosome 2 OCIAD1, SFTPD
endosome 2 OCIAD1, OPRM1
plasma membrane 8 APOA1, AQP2, CD2, HTR3A, HTT, OPRM1, TCIM, TPRA1
Membrane 7 AQP2, BLCAP, HTR3A, OCIAD1, OPRM1, PEF1, TPRA1
apical plasma membrane 1 AQP2
axon 2 HTT, OPRM1
basolateral plasma membrane 1 AQP2
extracellular exosome 4 APOA1, AQP2, PEF1, THBS4
endoplasmic reticulum 4 HTT, OPRM1, PEF1, THBS4
extracellular space 6 APOA1, CRP, INS, SFTPA1, SFTPD, THBS4
perinuclear region of cytoplasm 2 AQP2, HTT
mitochondrion 3 HK1, OCIAD1, STYXL1
protein-containing complex 2 CD2, HTT
Single-pass type I membrane protein 1 CD2
Secreted 5 APOA1, CRP, INS, SFTPA1, THBS4
extracellular region 7 APOA1, CD2, CRP, INS, SFTPA1, SFTPD, THBS4
cytoplasmic side of plasma membrane 1 CD2
Mitochondrion outer membrane 1 HK1
mitochondrial outer membrane 1 HK1
Mitochondrion matrix 1 STYXL1
mitochondrial matrix 1 STYXL1
external side of plasma membrane 1 CD2
Extracellular vesicle 1 APOA1
Secreted, extracellular space, extracellular matrix 2 SFTPA1, THBS4
chylomicron 1 APOA1
high-density lipoprotein particle 1 APOA1
low-density lipoprotein particle 1 APOA1
multivesicular body 2 SFTPA1, SFTPD
very-low-density lipoprotein particle 1 APOA1
perikaryon 1 OPRM1
cytoplasmic vesicle 1 APOA1
nucleolus 1 TCIM
Early endosome 2 APOA1, HTT
cell-cell junction 1 CD2
recycling endosome 1 AQP2
postsynaptic membrane 2 HTR3A, HTT
Apical cell membrane 1 AQP2
Membrane raft 2 HK1, HTT
Cell junction, focal adhesion 1 HTT
focal adhesion 1 HTT
basement membrane 1 THBS4
collagen trimer 2 SFTPA1, SFTPD
sarcoplasmic reticulum 1 THBS4
collagen-containing extracellular matrix 2 APOA1, THBS4
lateral plasma membrane 1 AQP2
nuclear speck 1 TCIM
Postsynaptic cell membrane 1 HTR3A
Late endosome 1 HTT
Cell projection, neuron projection 1 HTT
neuron projection 3 HTR3A, HTT, OPRM1
centriole 1 HTT
Secreted, extracellular space 1 THBS4
Nucleus, nucleolus 1 TCIM
blood microparticle 1 APOA1
serotonin-activated cation-selective channel complex 1 HTR3A
transmembrane transporter complex 1 HTR3A
Basolateral cell membrane 1 AQP2
Cul3-RING ubiquitin ligase complex 1 PEF1
Endomembrane system 1 HTT
endosome lumen 1 INS
Cytoplasmic vesicle membrane 2 AQP2, HTT
Cell projection, dendrite 1 OPRM1
Nucleus speckle 1 TCIM
secretory granule lumen 2 APOA1, INS
Golgi lumen 1 INS
endoplasmic reticulum lumen 2 APOA1, INS
endocytic vesicle 2 APOA1, SFTPD
transport vesicle 1 INS
Endoplasmic reticulum-Golgi intermediate compartment membrane 1 INS
clathrin-coated endocytic vesicle 2 SFTPA1, SFTPD
ER to Golgi transport vesicle membrane 1 PEF1
postsynaptic cytosol 1 HTT
Cytoplasmic vesicle, COPII-coated vesicle membrane 1 PEF1
COPII vesicle coat 1 PEF1
presynaptic cytosol 1 HTT
spherical high-density lipoprotein particle 1 APOA1
endocytic vesicle lumen 1 APOA1
transport vesicle membrane 1 AQP2
inclusion body 1 HTT
lamellar body 1 SFTPA1
serotonergic synapse 1 HTT
[Isoform 12]: Cytoplasm 1 OPRM1
lumenal side of membrane 1 AQP2
[Huntingtin]: Cytoplasm 1 HTT
[Huntingtin, myristoylated N-terminal fragment]: Cytoplasmic vesicle, autophagosome 1 HTT
Secreted, extracellular space, surface film 1 SFTPA1


文献列表

  • Petra Maleš, Ivana Nikšić-Franjić, Anna Wang, Barbara Pem, Danijela Bakarić. Optical and molecular features of negatively curved surfaces created by POPE lipids: A crucial role of the initial conditions. Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy. 2024 Sep; 317(?):124462. doi: 10.1016/j.saa.2024.124462. [PMID: 38754204]
  • Alessandro Crnjar, Carla Molteni. Cholesterol content in the membrane promotes key lipid-protein interactions in a pentameric serotonin-gated ion channel. Biointerphases. 2021 01; 15(6):061018. doi: 10.1116/6.0000561. [PMID: 33397116]
  • Aml A Alnaas, Abena Watson-Siriboe, Sherleen Tran, Mikias Negussie, Jack A Henderson, J Ryan Osterberg, Nara L Chon, Beckston M Harrott, Julianna Oviedo, Tatyana Lyakhova, Cole Michel, Nichole Reisdorph, Richard Reisdorph, Colin T Shearn, Hai Lin, Jefferson D Knight. Multivalent lipid targeting by the calcium-independent C2A domain of synaptotagmin-like protein 4/granuphilin. The Journal of biological chemistry. 2021 Jan; 296(?):100159. doi: 10.1074/jbc.ra120.014618. [PMID: 33277360]
  • Mehdi Azouz, Alexandre Therrien, Corinne Buré, Caroline Tokarski, Sophie Lecomte, Michel Lafleur. Lipid selectivity in detergent extraction from bilayers. Biochemical and biophysical research communications. 2020 10; 531(2):140-143. doi: 10.1016/j.bbrc.2020.07.065. [PMID: 32782150]
  • Ming Li, William T Heller, Chung-Hao Liu, Carrie Y Gao, Yutian Cai, Yiming Hou, Mu-Ping Nieh. Effects of fluidity and charge density on the morphology of a bicellar mixture - A SANS study. Biochimica et biophysica acta. Biomembranes. 2020 09; 1862(9):183315. doi: 10.1016/j.bbamem.2020.183315. [PMID: 32304755]
  • Laura J Fox, Lauren Matthews, Holly Stockdale, Supakit Pichai, Tim Snow, Robert M Richardson, Wuge H Briscoe. Structural changes in lipid mesophases due to intercalation of dendritic polymer nanoparticles: Swollen lamellae, suppressed curvature, and augmented structural disorder. Acta biomaterialia. 2020 03; 104(?):198-209. doi: 10.1016/j.actbio.2019.12.036. [PMID: 31904557]
  • Yunhan Zhang, Tongwei Chen, Zhimeng Pan, Xianbao Sun, Xue Yin, Miao He, Shiyan Xiao, Haojun Liang. Theoretical Insights into the Interactions between Star-Shaped Antimicrobial Polypeptides and Bacterial Membranes. Langmuir : the ACS journal of surfaces and colloids. 2018 11; 34(44):13438-13448. doi: 10.1021/acs.langmuir.8b02677. [PMID: 30350688]
  • S C Lopes, G Ivanova, B de Castro, P Gameiro. Revealing cardiolipins influence in the construction of a significant mitochondrial membrane model. Biochimica et biophysica acta. Biomembranes. 2018 11; 1860(11):2465-2477. doi: 10.1016/j.bbamem.2018.07.006. [PMID: 30040925]
  • Simou Sun, Anne M Sendecki, Saranya Pullanchery, Da Huang, Tinglu Yang, Paul S Cremer. Multistep Interactions between Ibuprofen and Lipid Membranes. Langmuir : the ACS journal of surfaces and colloids. 2018 09; 34(36):10782-10792. doi: 10.1021/acs.langmuir.8b01878. [PMID: 30148644]
  • 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]
  • Marta Kolasinska-Sojka, Magdalena Wlodek, Michal Szuwarzynski, Sami Kereiche, Lubomir Kovacik, Piotr Warszynski. Properties of POPC/POPE supported lipid bilayers modified with hydrophobic quantum dots on polyelectrolyte cushions. Colloids and surfaces. B, Biointerfaces. 2017 Oct; 158(?):667-674. doi: 10.1016/j.colsurfb.2017.07.046. [PMID: 28763774]
  • Chun Shen, Minmin Xue, Hu Qiu, Wanlin Guo. Insertion of Neurotransmitters into a Lipid Bilayer Membrane and Its Implication on Membrane Stability: A Molecular Dynamics Study. Chemphyschem : a European journal of chemical physics and physical chemistry. 2017 Mar; 18(6):626-633. doi: 10.1002/cphc.201601184. [PMID: 28054433]
  • Jordi H Borrell, M Teresa Montero, Òscar Domènech. Mapping phase diagrams of supported lipid bilayers by atomic force microscopy. Microscopy research and technique. 2017 01; 80(1):4-10. doi: 10.1002/jemt.22655. [PMID: 27001606]
  • Oscar D Bello, Sarah M Auclair, James E Rothman, Shyam S Krishnakumar. Using ApoE Nanolipoprotein Particles To Analyze SNARE-Induced Fusion Pores. Langmuir : the ACS journal of surfaces and colloids. 2016 Mar; 32(12):3015-23. doi: 10.1021/acs.langmuir.6b00245. [PMID: 26972604]
  • Magdalena Wlodek, Michal Szuwarzynski, Marta Kolasinska-Sojka. Effect of Supporting Polyelectrolyte Multilayers and Deposition Conditions on the Formation of 1-Palmitoyl-2-oleoyl-sn-glycero-3-phosphocholine/1-Palmitoyl-2-oleoyl-sn-glycero-3-phosphoethanolamine Lipid Bilayers. Langmuir : the ACS journal of surfaces and colloids. 2015 Sep; 31(38):10484-92. doi: 10.1021/acs.langmuir.5b02560. [PMID: 26334376]
  • Maksym Golub, Dieter Lott, Vasil M Garamus, Daniel Laipple, Michael Stoermer, Erik B Watkins, Andreas Schreyer, Regine Willumeit-Römer. Neutron study of phospholipids 1-palmitoyl-2-oleoyl-sn-glycero-3-phospho-ethanolamine spray coating on titanium implants. Biointerphases. 2015 Mar; 11(1):011002. doi: 10.1116/1.4938556. [PMID: 26714450]
  • I P Kompiang, W R Gibson. Effect of hypophysectomy and insulin on lipogenesis in cockerels. Hormone and metabolic research = Hormon- und Stoffwechselforschung = Hormones et metabolisme. 1976 Sep; 8(5):340-5. doi: 10.1055/s-0028-1093629. [PMID: 10239]