11,14,15-THETA (BioDeep_00000010160)

Main id: BioDeep_00000629500

 

human metabolite Endogenous


代谢物信息卡片


(5Z,8Z,12E)-11,14,15-Trihydroxyeicosa-5,8,12-trienoic acid

化学式: C20H34O5 (354.2406)
中文名称:
谱图信息: 最多检出来源 Homo sapiens(lipidomics) 57.26%

分子结构信息

SMILES: CCCCCC(C(C=CC(CC=CCC=CCCCC(=O)O)O)O)O
InChI: InChI=1S/C20H34O5/c1-2-3-9-13-18(22)19(23)16-15-17(21)12-10-7-5-4-6-8-11-14-20(24)25/h4,6-7,10,15-19,21-23H,2-3,5,8-9,11-14H2,1H3,(H,24,25)

描述信息

11,14,15-trihydroxyeicosatrienoic acid (11,14,15-THETA) is a metabolite of the 15-lipoxygenase (15-LO) pathway of arachidonic acid (AA). Increased amounts of 11,14,15-THETA are synthesized in subacute hypoxia. Prolonged exposure to reduced PO2 activates 15-LO in small pulmonary arteries (PA); activation of 15-LO is associated with translocation of the enzyme from the cytosol to membrane. 11,14,15-THETA is an endothelium-derived relaxing factor. (PMID: 12690037, 9812980, 15388505, 14622984) [HMDB]
11,14,15-trihydroxyeicosatrienoic acid (11,14,15-THETA) is a metabolite of the 15-lipoxygenase (15-LO) pathway of arachidonic acid (AA). Increased amounts of 11,14,15-THETA are synthesized in subacute hypoxia. Prolonged exposure to reduced PO2 activates 15-LO in small pulmonary arteries (PA); activation of 15-LO is associated with translocation of the enzyme from the cytosol to membrane. 11,14,15-THETA is an endothelium-derived relaxing factor. (PMID: 12690037, 9812980, 15388505, 14622984).

同义名列表

18 个代谢物同义名

(5Z,8Z,12E)-11,14,15-Trihydroxyeicosa-5,8,12-trienoic acid; (5Z,8Z,12E)-11,14,15-Trihydroxyicosa-5,8,12-trienoic acid; (5Z,8Z,12E)-11,14,15-Trihydroxyeicosa-5,8,12-trienoate; (5Z,8Z,12E)-11,14,15-Trihydroxyicosa-5,8,12-trienoate; 11,14,15-Trihydroxy-(5Z,8Z,12E)-eicosatrienoic acid; (5Z,8Z,12E)-11,14,15-Trihydroxyeicosatrienoic acid; (5Z,8Z,12E)-11,14,15-Trihydroxyicosatrienoic acid; 11,14,15-trihydroxy-5Z,8Z,12E-eicosatrienoic acid; 11,14,15-Trihydroxy-(5Z,8Z,12E)-eicosatrienoate; 11,14,15-Trihydroxyeicosa-5,8,12-trienoic acid; (5Z,8Z,12E)-11,14,15-Trihydroxyeicosatrienoate; (5Z,8Z,12E)-11,14,15-Trihydroxyicosatrienoate; 11,14,15-Trihydroxy-5Z,8Z,12E-eicosatrienoate; 11,14,15-Trihydroxyeicosatetraenoic acid; 11,14,15-Trihydroxyicosatrienoic acid; 11,14,15-Trihydroxyicosatrienoate; 11,14,15-THETA; 11,14,15-THET



数据库引用编号

12 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

46 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(46)

PharmGKB(0)

1 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

  • S L Pfister, N Spitzbarth, K Nithipatikom, W S Edgemond, J R Falck, W B Campbell. Identification of the 11,14,15- and 11,12, 15-trihydroxyeicosatrienoic acids as endothelium-derived relaxing factors of rabbit aorta. The Journal of biological chemistry. 1998 Nov; 273(47):30879-87. doi: 10.1074/jbc.273.47.30879. [PMID: 9812980]
  • H Y Ho, P Y Wong. Transformation of 15-hydroperoxide of eicosapentaenoic acid to lipoxins and trihydroxyeicosatetraenoic acids by 5-lipoxygenase partially purified from potato tubers. Eicosanoids. 1990; 3(2):99-104. doi: . [PMID: 2206562]
  • R H Weiss, J L Arnold, R W Estabrook. Transformation of an arachidonic acid hydroperoxide into epoxyhydroxy and trihydroxy fatty acids by liver microsomal cytochrome P-450. Archives of biochemistry and biophysics. 1987 Jan; 252(1):334-8. doi: 10.1016/0003-9861(87)90039-7. [PMID: 3813540]