PC 36:1 (BioDeep_00000410754)

   

LipidSearch


代谢物信息卡片


1-(11Z-octadecenoyl)-2-octadecanoyl-sn-glycero-3-phosphocholine

化学式: C44H86NO8P (787.6090726)
中文名称:
谱图信息: 最多检出来源 Homo sapiens(lipidomics) 45.83%

分子结构信息

SMILES: CCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCC=CCCCCCCCC)COP(=O)([O-])OCC[N+](C)(C)C
InChI: InChI=1S/C44H86NO8P/c1-6-8-10-12-14-16-18-19-20-21-22-23-24-25-27-28-30-32-34-36-43(46)50-40-42(41-52-54(48,49)51-39-38-45(3,4)5)53-44(47)37-35-33-31-29-26-17-15-13-11-9-7-2/h19-20,42H,6-18,21-41H2,1-5H3/b20-19-/t42-/m1/s1

描述信息

Found in mouse brain; TwoDicalId=66; MgfFile=160720_brain_EPA_08_Neg; MgfId=1487

同义名列表

73 个代谢物同义名

1-(13Z-docosenoyl)-2-tetradecanoyl-sn-glycero-3-phosphocholine; PC(22:1(13Z)/14:0); PC(14:0_22:1); PC(36:1); PC 36:1; 1-tetradecanoyl-2-(13Z-docosenoyl)-sn-glycero-3-phosphocholine; PC(14:0/22:1(13Z)); 1-(11Z-docosenoyl)-2-tetradecanoyl-glycero-3-phosphocholine; PC(22:1(11Z)/14:0); 1-docosanoyl-2-(9Z-tetradecenoyl)-glycero-3-phosphocholine; PC(22:0/14:1(9Z)); PC(14:1_22:0); 1-heneicosanoyl-2-(9Z-pentadecenoyl)-glycero-3-phosphocholine; PC(21:0/15:1(9Z)); PC(15:1_21:0); 1-(11Z-eicosenoyl)-2-hexadecanoyl-glycero-3-phosphocholine; PC(20:1(11Z)/16:0); PC(16:0_20:1); 1-eicosanoyl-2-(9Z-hexadecenoyl)-glycero-3-phosphocholine; PC(20:0/16:1(9Z)); PC(16:1_20:0); 1-(9Z-nonadecenoyl)-2-heptadecanoyl-glycero-3-phosphocholine; PC(19:1(9Z)/17:0); PC(17:0_19:1); 1-nonadecanoyl-2-(9Z-heptadecenoyl)-glycero-3-phosphocholine; PC(19:0/17:1(9Z)); PC(17:1_19:0); 1-(9Z-heptadecenoyl)-2-nonadecanoyl-glycero-3-phosphocholine; PC(17:1(9Z)/19:0); 1-heptadecanoyl-2-(9Z-nonadecenoyl)-glycero-3-phosphocholine; PC(17:0/19:1(9Z)); 1-(9Z-hexadecenoyl)-2-eicosanoyl-glycero-3-phosphocholine; PC(16:1(9Z)/20:0); 1-hexadecanoyl-2-(11Z-eicosenoyl)-glycero-3-phosphocholine; PC(16:0/20:1(11Z)); 1-(9Z-pentadecenoyl)-2-heneicosanoyl-glycero-3-phosphocholine; PC(15:1(9Z)/21:0); 1-(9Z-tetradecenoyl)-2-docosanoyl-glycero-3-phosphocholine; PC(14:1(9Z)/22:0); 1-tetradecanoyl-2-(11Z-docosenoyl)-glycero-3-phosphocholine; PC(14:0/22:1(11Z)); 1-(9Z-octadecenoyl)-2-octadecanoyl-sn-glycero-3-phosphocholine; Choline phosphate, 3-ester with L-1-oleo-2-stearin; L-1-Oleoyl-2-stearoyl-3-phosphatidylcholine; L-1-Oleoyl-2-stearoyl lecithin; PC(18:1(9Z)/18:0); PC(18:1/18:0); PC(18:0_18:1); OSPC; 1-(11Z-octadecenoyl)-2-octadecanoyl-sn-glycero-3-phosphocholine; PC(18:1(11Z)/18:0); 1-octadecanoyl-2-(9Z-octadecenoyl)-sn-glycero-3-phosphocholine; Choline phosphate, 3-ester with L-2-oleo-1-stearin; 1-Stearoyl-2-oleoyl-sn-glycero-3-phosphocholine; L-alpha-1-Stearoyl-2-oleoylphosphatidylcholine; L-alpha-1-Stearoyl-2-oleoyl lecithin; PC(18:0/18:1(9Z)); PC(18:0/18:1); SOPC; 1-octadecanoyl-2-(9E-octadecenoyl)-sn-glycero-3-phosphocholine; PC(18:0/18:1(9E)); 1-octadecanoyl-2-(7Z-octadecenoyl)-sn-glycero-3-phosphocholine; PC(18:0/18:1(7Z)); 1-octadecanoyl-2-(6Z-octadecenoyl)-sn-glycero-3-phosphocholine; PC(18:0/18:1(6Z)); 1-octadecanoyl-2-(16Z-octadecenoyl)-sn-glycero-3-phosphocholine; PC(18:0/18:1(16Z)); 1-octadecanoyl-2-(13Z-octadecenoyl)-sn-glycero-3-phosphocholine; PC(18:0/18:1(13Z)); 1-octadecanoyl-2-(12Z-octadecenoyl)-sn-glycero-3-phosphocholine; PC(18:0/18:1(12Z)); 1-octadecanoyl-2-(11Z-octadecenoyl)-sn-glycero-3-phosphocholine; PC(18:0/18:1(11Z))



数据库引用编号

62 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

24 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(24)

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

  • Poornima Budime Santhosh, Tihomir Tenev, Luka Šturm, Nataša Poklar Ulrih, Julia Genova. Effects of Hydrophobic Gold Nanoparticles on Structure and Fluidity of SOPC Lipid Membranes. International journal of molecular sciences. 2023 Jun; 24(12):. doi: 10.3390/ijms241210226. [PMID: 37373371]
  • Shea Foley, Elizabeth Miller, Samuel Braziel, Sunghee Lee. Molecular organization in mixed SOPC and SDPC model membranes: Water permeability studies of polyunsaturated lipid bilayers. Biochimica et biophysica acta. Biomembranes. 2020 09; 1862(9):183365. doi: 10.1016/j.bbamem.2020.183365. [PMID: 32454009]
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  • Hung-Hsun Lee, Martynas Gavutis, Živilė Ruželė, Ramu Nas Valiokas, Bo Liedberg. Mixed Self-Assembled Monolayers with Terminal Deuterated Anchors: Characterization and Probing of Model Lipid Membrane Formation. The journal of physical chemistry. B. 2018 08; 122(34):8201-8210. doi: 10.1021/acs.jpcb.8b05097. [PMID: 30085662]
  • 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]
  • Soohyung Park, Wonpil Im. Quantitative Characterization of Cholesterol Partitioning between Binary Bilayers. Journal of chemical theory and computation. 2018 Jun; 14(6):2829-2833. doi: 10.1021/acs.jctc.8b00140. [PMID: 29733641]
  • Julien Massiot, Ali Makky, Florent Di Meo, David Chapron, Patrick Trouillas, Véronique Rosilio. Impact of lipid composition and photosensitizer hydrophobicity on the efficiency of light-triggered liposomal release. Physical chemistry chemical physics : PCCP. 2017 May; 19(18):11460-11473. doi: 10.1039/c7cp00983f. [PMID: 28425533]
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  • Chiu-Hao Chen, Sárka Málková, Sai Venkatesh Pingali, Fei Long, Shekhar Garde, Wonhwa Cho, Mark L Schlossman. Configuration of PKCalpha-C2 domain bound to mixed SOPC/SOPS lipid monolayers. Biophysical journal. 2009 Nov; 97(10):2794-802. doi: 10.1016/j.bpj.2009.08.037. [PMID: 19917234]
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  • Jianjun Pan, Thalia T Mills, Stephanie Tristram-Nagle, John F Nagle. Cholesterol perturbs lipid bilayers nonuniversally. Physical review letters. 2008 May; 100(19):198103. doi: 10.1103/physrevlett.100.198103. [PMID: 18518492]
  • Rohit Sood, Yegor Domanov, Milla Pietiäinen, Vesa P Kontinen, Paavo K J Kinnunen. Binding of LL-37 to model biomembranes: insight into target vs host cell recognition. Biochimica et biophysica acta. 2008 Apr; 1778(4):983-96. doi: 10.1016/j.bbamem.2007.11.016. [PMID: 18166145]
  • Alexander I Greenwood, Jianjun Pan, Thalia T Mills, John F Nagle, Richard M Epand, Stephanie Tristram-Nagle. CRAC motif peptide of the HIV-1 gp41 protein thins SOPC membranes and interacts with cholesterol. Biochimica et biophysica acta. 2008 Apr; 1778(4):1120-30. doi: 10.1016/j.bbamem.2008.01.008. [PMID: 18262490]
  • Gary J Dever, Robert Benson, Cherry L Wainwright, Simon Kennedy, Corinne M Spickett. Phospholipid chlorohydrin induces leukocyte adhesion to ApoE-/- mouse arteries via upregulation of P-selectin. Free radical biology & medicine. 2008 Feb; 44(3):452-63. doi: 10.1016/j.freeradbiomed.2007.10.038. [PMID: 18005671]
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  • Sumit Garg, Jürgen Rühe, Karin Lüdtke, Rainer Jordan, Christoph A Naumann. Domain registration in raft-mimicking lipid mixtures studied using polymer-tethered lipid bilayers. Biophysical journal. 2007 Feb; 92(4):1263-70. doi: 10.1529/biophysj.106.091082. [PMID: 17114215]
  • Valeriya M Ioffe, Galyna P Gorbenko, P K J Kinnunen, Anatoliy L Tatarets, Olga S Kolosova, Leonid D Patsenker, Ewald A Terpetschnig. Tracing lysozyme-lipid interactions with long-wavelength squaraine dyes. Journal of fluorescence. 2007 Jan; 17(1):65-72. doi: 10.1007/s10895-006-0142-4. [PMID: 17192821]
  • Ivan V Polozov, Klaus Gawrisch. NMR detection of lipid domains. Methods in molecular biology (Clifton, N.J.). 2007; 398(?):107-26. doi: 10.1007/978-1-59745-513-8_9. [PMID: 18214377]
  • Sárka Málková, Robert V Stahelin, Sai V Pingali, Wonhwa Cho, Mark L Schlossman. Orientation and penetration depth of monolayer-bound p40phox-PX. Biochemistry. 2006 Nov; 45(45):13566-75. doi: 10.1021/bi061133l. [PMID: 17087510]
  • Feng Gao, Erwen Mei, Manho Lim, Robin M Hochstrasser. Probing lipid vesicles by bimolecular association and dissociation trajectories of single molecules. Journal of the American Chemical Society. 2006 Apr; 128(14):4814-22. doi: 10.1021/ja058098a. [PMID: 16594718]
  • Y Gambin, R Lopez-Esparza, M Reffay, E Sierecki, N S Gov, M Genest, R S Hodges, W Urbach. Lateral mobility of proteins in liquid membranes revisited. Proceedings of the National Academy of Sciences of the United States of America. 2006 Feb; 103(7):2098-102. doi: 10.1073/pnas.0511026103. [PMID: 16461891]
  • Sárka Málková, Fei Long, Robert V Stahelin, Sai V Pingali, Diana Murray, Wonhwa Cho, Mark L Schlossman. X-ray reflectivity studies of cPLA2{alpha}-C2 domains adsorbed onto Langmuir monolayers of SOPC. Biophysical journal. 2005 Sep; 89(3):1861-73. doi: 10.1529/biophysj.105.061515. [PMID: 15994899]
  • Yong Zhou, Robert M Raphael. Effect of salicylate on the elasticity, bending stiffness, and strength of SOPC membranes. Biophysical journal. 2005 Sep; 89(3):1789-801. doi: 10.1529/biophysj.104.054510. [PMID: 15951377]
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  • Oliver Purrucker, Anton Förtig, Karin Lüdtke, Rainer Jordan, Motomu Tanaka. Confinement of transmembrane cell receptors in tunable stripe micropatterns. Journal of the American Chemical Society. 2005 Feb; 127(4):1258-64. doi: 10.1021/ja045713m. [PMID: 15669865]
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