(10E,12Z)-(9S)-9-Hydroperoxyoctadeca-10,12-dienoic acid (BioDeep_00000055078)

Main id: BioDeep_00000003310

 

human metabolite Endogenous Volatile Flavor Compounds


代谢物信息卡片


(9S,10E,12Z,15Z)-9-Hydroperoxy-10,12,15-octadecadienoic acid

化学式: C18H32O4 (312.2300472)
中文名称:
谱图信息: 最多检出来源 Homo sapiens(lipidomics) 0.12%

分子结构信息

SMILES: C(CCCCCCC[C@H](OO)/C=C/C=C\CCCCC)(=O)O
InChI: InChI=1S/C18H32O4/c1-2-3-4-5-6-8-11-14-17(22-21)15-12-9-7-10-13-16-18(19)20/h6,8,11,14,17,21H,2-5,7,9-10,12-13,15-16H2,1H3,(H,19,20)/b8-6-,14-11+/t17-/m1/s1

描述信息

(9s,10e,12z,15z)-9-hydroperoxy-10,12,15-octadecadienoate, also known as 9(S)-hpod or 9-hydroperoxy-11,12-octadecadienoic acid, belongs to lineolic acids and derivatives class of compounds. Those are derivatives of lineolic acid. Lineolic acid is a polyunsaturated omega-6 18 carbon long fatty acid, with two CC double bonds at the 9- and 12-positions. Thus, (9s,10e,12z,15z)-9-hydroperoxy-10,12,15-octadecadienoate is considered to be an octadecanoid lipid molecule (9s,10e,12z,15z)-9-hydroperoxy-10,12,15-octadecadienoate is practically insoluble (in water) and a weakly acidic compound (based on its pKa). (9s,10e,12z,15z)-9-hydroperoxy-10,12,15-octadecadienoate can be found in a number of food items such as burdock, oat, parsnip, and cocoa bean, which makes (9s,10e,12z,15z)-9-hydroperoxy-10,12,15-octadecadienoate a potential biomarker for the consumption of these food products.
(10E,12Z)-(9S)-9-Hydroperoxyoctadeca-10,12-dienoic acid, also known as 9(S)-HPOD or (9S,10E,12Z)-9-Hydroperoxy-10,12-octadecadienoate, is classified as a lineolic acid or a Lineolic acid derivative. Lineolic acids are derivatives of lineolic acid. Lineolic acid is a polyunsaturated omega-6 18 carbon long fatty acid, with two CC double bonds at the 9- and 12-positions. (10E,12Z)-(9S)-9-Hydroperoxyoctadeca-10,12-dienoic acid is considered to be practically insoluble (in water) and acidic. (10E,12Z)-(9S)-9-Hydroperoxyoctadeca-10,12-dienoic acid is an octadecanoid lipid molecule. (10E,12Z)-(9S)-9-Hydroperoxyoctadeca-10,12-dienoic acid can be found throughout numerous foods such as Barley, Prunus (Cherry, Plum), Cherimoya, and Prairie turnips
D004791 - Enzyme Inhibitors > D016859 - Lipoxygenase Inhibitors
D009676 - Noxae > D016877 - Oxidants > D010545 - Peroxides

同义名列表

17 个代谢物同义名

(9S,10E,12Z,15Z)-9-Hydroperoxy-10,12,15-octadecadienoic acid; (9S,10E,12Z,15Z)-9-hydroperoxy-10,12,15-octadecadienoate; (10E,12Z)-(9S)-9-Hydroperoxyoctadeca-10,12-dienoic acid; 9-Hydroperoxy-11,12-octadecadienoic acid, (Z,e)-isomer; 9-Hydroperoxy-11,12-octadecadienoic acid, (e,Z)-isomer; (9S,10E,12Z)-9-Hydroperoxy-10,12-octadecadienoic acid; (9S,10E,12Z)-9-hydroperoxyoctadeca-10,12-dienoic acid; (10E,12Z)-(9S)-9-Hydroperoxyoctadeca-10,12-dienoate; (9S,10E,12Z)-9-Hydroperoxy-10,12-octadecadienoate; 9S-hydroperoxy-10E,12Z-octadecadienoic acid; 9-Hydroperoxy-11,12-octadecadienoic acid; FA 18:2;O2; 9(S)-HPODE; 9(S)-HPOD; 9S-HpODE; 9-HpODE; 9(S)-HPODE



数据库引用编号

13 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)

5 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

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  • Markus K Muellner, Sabine M Schreier, Hilde Laggner, Marcela Hermann, Harald Esterbauer, Markus Exner, Bernhard M K Gmeiner, Stylianos Kapiotis. Hydrogen sulfide destroys lipid hydroperoxides in oxidized LDL. The Biochemical journal. 2009 May; 420(2):277-81. doi: 10.1042/bj20082421. [PMID: 19265508]
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  • Wei-Gen Li, Lynn L Stoll, James B Rice, Shao-Ping Xu, Francis J Miller, Papri Chatterjee, Ling Hu, Larry W Oberley, Arthur A Spector, Neal L Weintraub. Activation of NAD(P)H oxidase by lipid hydroperoxides: mechanism of oxidant-mediated smooth muscle cytotoxicity. Free radical biology & medicine. 2003 Apr; 34(7):937-46. doi: 10.1016/s0891-5849(03)00032-7. [PMID: 12654483]
  • Alberto Nuñez, Brett J Savary, Thomas A Foglia, George J Piazza. Purification of lipoxygenase from Chlorella: production of 9- and 13-hydroperoxide derivatives of linoleic acid. Lipids. 2002 Nov; 37(11):1027-32. doi: 10.1007/s11745-002-0996-x. [PMID: 12558051]
  • Yoshihiko Akakabe, Kenji Matsui, Tadahiko Kajiwara. Enantioselective formation of (R)-9-HPODE and (R)-9-HPOTrE in marine green alga Ulva conglobata. Bioorganic & medicinal chemistry. 2002 Oct; 10(10):3171-3. doi: 10.1016/s0968-0896(02)00212-2. [PMID: 12150862]
  • Heiko Weichert, Adelheid Kolbe, Angelika Kraus, Claus Wasternack, Ivo Feussner. Metabolic profiling of oxylipins in germinating cucumber seedlings--lipoxygenase-dependent degradation of triacylglycerols and biosynthesis of volatile aldehydes. Planta. 2002 Aug; 215(4):612-9. doi: 10.1007/s00425-002-0779-4. [PMID: 12172844]
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