(2'E,4'Z,8E)-Colneleic acid (BioDeep_00000004356)

 

Secondary id: BioDeep_00000631102

human metabolite Endogenous Volatile Flavor Compounds natural product


代谢物信息卡片


(8E)-9-[(1E,3Z)-Nona-1,3-dien-1-yloxy]non-8-enoic acid

化学式: C18H30O3 (294.21948299999997)
中文名称:
谱图信息: 最多检出来源 Viridiplantae(plant) 13.2%

分子结构信息

SMILES: C(C/C=C\C=C\O/C=C/CCCCCCC(=O)O)CCC
InChI: InChI=1S/C18H30O3/c1-2-3-4-5-7-10-13-16-21-17-14-11-8-6-9-12-15-18(19)20/h7,10,13-14,16-17H,2-6,8-9,11-12,15H2,1H3,(H,19,20)/b10-7-,16-13+,17-14+

描述信息

Product of the enzymic oxidation of potato lipids. (2E,4Z,8E)-Colneleic acid is found in alcoholic beverages and potato.
(2E,4Z,8E)-Colneleic acid is found in alcoholic beverages. Product of the enzymic oxidation of potato lipid

同义名列表

16 个代谢物同义名

(8E)-9-[(1E,3Z)-Nona-1,3-dien-1-yloxy]non-8-enoic acid; (8E)-9-[(1E,3Z)-Nona-1,3-dien-1-yloxy]non-8-enoate; (8E,1e,3z)-9-(1,3-Nonadienyloxy)-8-nonenoic acid; 9-(1,3-Nonadienyloxy)-(e,e,Z)-8-nonenoic acid; (8E,1e,3z)-9-(1,3-Nonadienyloxy)-8-nonenoate; 9-[1E,3Z-dien-1-yloxy]-non-8E-enoic acid; 9-(Nona-1,3-dienoxy)non-8-enoic acid; 9-nona-1,3-dienoxynon-8-enoic acid; (2E,4Z,8E)-Colneleic acid; (2e,4z,8E)-Colneleate; 9-Oxa-8t10t12c-C18:3; 9-Oxa-8t10t12c-18:3; Colneleinsaeure; Colneleic acid; Colneleate; Colneleate



数据库引用编号

15 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)

12 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

  • Guillaume Saubeau, Sophie Goulitquer, Dominique Barloy, Philippe Potin, Didier Andrivon, Florence Val. Differential induction of oxylipin pathway in potato and tobacco cells by bacterial and oomycete elicitors. Plant cell reports. 2013 May; 32(5):579-89. doi: 10.1007/s00299-012-1377-y. [PMID: 23479199]
  • Martin Mariutto, Francéline Duby, Akram Adam, Charlotte Bureau, Marie-Laure Fauconnier, Marc Ongena, Philippe Thonart, Jacques Dommes. The elicitation of a systemic resistance by Pseudomonas putida BTP1 in tomato involves the stimulation of two lipoxygenase isoforms. BMC plant biology. 2011 Feb; 11(?):29. doi: 10.1186/1471-2229-11-29. [PMID: 21294872]
  • Marie-Laure Fauconnier, Jorge Rojas-Beltran, Brice Dupuis, Pierre Delaplace, Patrick Frettinger, Virginie Gosset, Patrick du Jardin. Changes in oxylipin synthesis after Phytophthora infestans infection of potato leaves do not correlate with resistance. Plant physiology and biochemistry : PPB. 2008 Aug; 46(8-9):823-31. doi: 10.1016/j.plaphy.2008.04.010. [PMID: 18538577]
  • Ren Wang, Wenbiao Shen, Linglong Liu, Ling Jiang, Yuqiang Liu, Ning Su, Jianmin Wan. A novel lipoxygenase gene from developing rice seeds confers dual position specificity and responds to wounding and insect attack. Plant molecular biology. 2008 Mar; 66(4):401-14. doi: 10.1007/s11103-007-9278-0. [PMID: 18185911]
  • Lennart Eschen-Lippold, Grit Rothe, Michael Stumpe, Cornelia Göbel, Ivo Feussner, Sabine Rosahl. Reduction of divinyl ether-containing polyunsaturated fatty acids in transgenic potato plants. Phytochemistry. 2007 Mar; 68(6):797-801. doi: 10.1016/j.phytochem.2006.12.010. [PMID: 17258245]
  • Tracy Cowley, Dale Walters. Local and systemic effects of oxylipins on powdery mildew infection in barley. Pest management science. 2005 Jun; 61(6):572-6. doi: 10.1002/ps.1026. [PMID: 15668923]
  • Mats Hamberg. Hidden stereospecificity in the biosynthesis of divinyl ether fatty acids. The FEBS journal. 2005 Feb; 272(3):736-43. doi: 10.1111/j.1742-4658.2004.04510.x. [PMID: 15670154]
  • Marie Laure Fauconnier, Ruth Welti, Elizabeth Blée, Michel Marlier. Lipid and oxylipin profiles during aging and sprout development in potato tubers (Solanum tuberosum L.). Biochimica et biophysica acta. 2003 Jul; 1633(2):118-26. doi: 10.1016/s1388-1981(03)00105-7. [PMID: 12880871]
  • Cornelia Göbel, Ivo Feussner, Mats Hamberg, Sabine Rosahl. Oxylipin profiling in pathogen-infected potato leaves. Biochimica et biophysica acta. 2002 Sep; 1584(1):55-64. doi: 10.1016/s1388-1981(02)00268-8. [PMID: 12213493]
  • M Stumpe, R Kandzia, C Göbel, S Rosahl, I Feussner. A pathogen-inducible divinyl ether synthase (CYP74D) from elicitor-treated potato suspension cells. FEBS letters. 2001 Nov; 507(3):371-6. doi: 10.1016/s0014-5793(01)03019-8. [PMID: 11696374]
  • C Göbel, I Feussner, A Schmidt, D Scheel, J Sanchez-Serrano, M Hamberg, S Rosahl. Oxylipin profiling reveals the preferential stimulation of the 9-lipoxygenase pathway in elicitor-treated potato cells. The Journal of biological chemistry. 2001 Mar; 276(9):6267-73. doi: 10.1074/jbc.m008606200. [PMID: 11085991]
  • A Itoh, G A Howe. Molecular cloning of a divinyl ether synthase. Identification as a CYP74 cytochrome P-450. The Journal of biological chemistry. 2001 Feb; 276(5):3620-7. doi: 10.1074/jbc.m008964200. [PMID: 11060314]
  • H Weber, A Chételat, D Caldelari, E E Farmer. Divinyl ether fatty acid synthesis in late blight-diseased potato leaves. The Plant cell. 1999 Mar; 11(3):485-94. doi: 10.1105/tpc.11.3.485. [PMID: 10072406]
  • M Hamberg. A pathway for biosynthesis of divinyl ether fatty acids in green leaves. Lipids. 1998 Nov; 33(11):1061-71. doi: 10.1007/s11745-998-0306-7. [PMID: 9870900]
  • A N Grechkin, A V Ilyasov, M Hamberg. On the mechanism of biosynthesis of divinyl ether oxylipins by enzyme from garlic bulbs. European journal of biochemistry. 1997 Apr; 245(1):137-42. doi: 10.1111/j.1432-1033.1997.00137.x. [PMID: 9128734]