2553-17-5 (BioDeep_00000860517)

Main id: BioDeep_00000015367

 

Volatile Flavor Compounds


代谢物信息卡片


9-ketopelargonic acid

化学式: C9H16O3 (172.10993860000002)
中文名称: 9-氧代壬酸
谱图信息: 最多检出来源 () 0%

分子结构信息

SMILES: C(CCCC=O)CCCC(=O)O
InChI: InChI=1S/C9H16O3/c10-8-6-4-2-1-3-5-7-9(11)12/h8H,1-7H2,(H,11,12)

描述信息

同义名列表

10 个代谢物同义名

9-ketopelargonic acid; Nonanoic acid, 9-oxo-; 9-oxo-nonanoic acid; 9-Ketononanoic acid; 9-Oxononanoic acid; LMFA01060160; 2553-17-5; C16322; 9-Oxononanoic acid; 9-Oxononanoic acid



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)

10 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

  • Miguel A López, Jorge Vicente, Satish Kulasekaran, Tamara Vellosillo, Marta Martínez, Maria L Irigoyen, Tomas Cascón, Gerard Bannenberg, Mats Hamberg, Carmen Castresana. Antagonistic role of 9-lipoxygenase-derived oxylipins and ethylene in the control of oxidative stress, lipid peroxidation and plant defence. The Plant journal : for cell and molecular biology. 2011 Aug; 67(3):447-58. doi: 10.1111/j.1365-313x.2011.04608.x. [PMID: 21481031]
  • Fong-Chin Huang, Wilfried Schwab. Cloning and characterization of a 9-lipoxygenase gene induced by pathogen attack from Nicotiana benthamiana for biotechnological application. BMC biotechnology. 2011 Mar; 11(?):30. doi: 10.1186/1472-6750-11-30. [PMID: 21450085]
  • Matthew E Szapacs, Hye-Young H Kim, Ned A Porter, Daniel C Liebler. Identification of proteins adducted by lipid peroxidation products in plasma and modifications of apolipoprotein A1 with a novel biotinylated phospholipid probe. Journal of proteome research. 2008 Oct; 7(10):4237-46. doi: 10.1021/pr8001222. [PMID: 18778096]
  • Jirasak Wong-Ekkabut, Zhitao Xu, Wannapong Triampo, I-Ming Tang, D Peter Tieleman, Luca Monticelli. Effect of lipid peroxidation on the properties of lipid bilayers: a molecular dynamics study. Biophysical journal. 2007 Dec; 93(12):4225-36. doi: 10.1529/biophysj.107.112565. [PMID: 17766354]
  • Alexander N Grechkin, Fredi Brühlmann, Lucia S Mukhtarova, Yuri V Gogolev, Mats Hamberg. Hydroperoxide lyases (CYP74C and CYP74B) catalyze the homolytic isomerization of fatty acid hydroperoxides into hemiacetals. Biochimica et biophysica acta. 2006 Dec; 1761(12):1419-28. doi: 10.1016/j.bbalip.2006.09.002. [PMID: 17049304]
  • N Tijet, C Schneider, B L Muller, A R Brash. Biogenesis of volatile aldehydes from fatty acid hydroperoxides: molecular cloning of a hydroperoxide lyase (CYP74C) with specificity for both the 9- and 13-hydroperoxides of linoleic and linolenic acids. Archives of biochemistry and biophysics. 2001 Feb; 386(2):281-9. doi: 10.1006/abbi.2000.2218. [PMID: 11368353]
  • S Minamoto, K Kanazawa, H Ashida, M Natake. Effect of orally administered 9-oxononanoic acid on lipogenesis in rat liver. Biochimica et biophysica acta. 1988 Feb; 958(2):199-204. doi: 10.1016/0005-2760(88)90177-4. [PMID: 2892534]