FA 20:5;O2 (BioDeep_00000629371)

 

Secondary id: BioDeep_00000006011, BioDeep_00000006017, BioDeep_00000010161, BioDeep_00000018157, BioDeep_00000054986, BioDeep_00000596139, BioDeep_00000895364, BioDeep_00001868832, BioDeep_00001869086

LipidSearch


代谢物信息卡片


4-((1R,5S)-5-((R,1E,5Z)-3-hydroxyundeca-1,5-dien-1-yl)-4-oxocyclopent-2-en-1-yl)butanoic acid

化学式: C20H30O4 (334.214398)
中文名称:
谱图信息: 最多检出来源 Macaca mulatta(otcml) 0.03%

分子结构信息

SMILES: C(/C=C/C=C/[C@@H]1O[C@H]1CCCC(=O)O)=C/C=C/[C@@H](O)CCCCC
InChI: InChI=1S/C20H30O4/c1-2-3-6-9-17(21)14-12-16-13-15-19(22)18(16)10-7-4-5-8-11-20(23)24/h4,7,13,15-16,18H,2-3,5-6,8-12,14H2,1H3,(H,23,24)/b7-4-/t16-,18+/m0/s1

描述信息

An oxylipin that is the (5S,6S)-epoxy-(15S)-hydroxy derivative of 7E,9E,11Z,13E-icosa-7,9,11,13-tetraenoic acid.
D000890 - Anti-Infective Agents > D000998 - Antiviral Agents
D000970 - Antineoplastic Agents

同义名列表

212 个代谢物同义名

(7E,9E,11Z,13E)-(5S,6S,15S)-5,6-Epoxy-15-hydroxyeicosa-7,9,11,13-tetraenoic acid; (7E,9E,11Z,13E)-(5S,6S,15S)-5,6-Epoxy-15-hydroxyicosa-7,9,11,13-tetraenoic acid; 5S,6S-epoxy-15S-hydroxy-7E,9E,11Z,13E-eicosatetraenoic acid; 5,6-Epoxytetraene; 5,6-Ep-15S-HETE; FA 20:5;O2; (R,5Z,9E)-8-hydroxy-10-((1R,5S)-4-oxo-5-pentylcyclopent-2-en-1-yl)deca-5,9-dienoic acid; (8R)-8-J2-IsoP[11R,15R]; 8,11-diepi-8-J2-IsoP; (S,5Z,9E)-8-hydroxy-10-((1R,5S)-4-oxo-5-pentylcyclopent-2-en-1-yl)deca-5,9-dienoic acid; (8S)-8-J2-IsoP[11R,15R]; 11-epi-8-J2-IsoP; (S,5Z,9E)-8-hydroxy-10-((1S,5R)-4-oxo-5-pentylcyclopent-2-en-1-yl)deca-5,9-dienoic acid; ent-8,11-diepi-8-J2-IsoP; (8S)-8-J2-IsoP[11S,15S]; (R,5Z,9E)-8-hydroxy-10-((1S,5R)-4-oxo-5-pentylcyclopent-2-en-1-yl)deca-5,9-dienoic acid; (8R)-8-J2-IsoP[11S,15S]; ent-11-epi-8-J2-IsoP; (R,E)-5-hydroxy-7-((S,E)-2-((Z)-oct-2-en-1-ylidene)-3-oxocyclopentyl)hept-6-enoic acid; (5R)-5-J2-IsoP[8R,12R]; 5,8-diepi-5-J2-IsoP; (S,E)-5-hydroxy-7-((S,E)-2-((Z)-oct-2-en-1-ylidene)-3-oxocyclopentyl)hept-6-enoic acid; (5S)-5-J2-IsoP[8R,12R]; 8-epi-5-J2-IsoP; (S,E)-5-hydroxy-7-((R,E)-2-((Z)-oct-2-en-1-ylidene)-3-oxocyclopentyl)hept-6-enoic acid; ent-5,8-diepi-5-J2-IsoP; (5S)-5-J2-IsoP[8S,12S]; (R,E)-5-hydroxy-7-((R,E)-2-((Z)-oct-2-en-1-ylidene)-3-oxocyclopentyl)hept-6-enoic acid; (5R)-5-J2-IsoP[8S,12S]; ent-8-epi-5-J2-IsoP; 4-((1R,5S)-5-((R,1E,5Z)-3-hydroxyundeca-1,5-dien-1-yl)-4-oxocyclopent-2-en-1-yl)butanoic acid; (12R)-12-J2-IsoP[5S,9R]; 5,12-diepi-12-J2-IsoP; 4-((1R,5S)-5-((S,1E,5Z)-3-hydroxyundeca-1,5-dien-1-yl)-4-oxocyclopent-2-en-1-yl)butanoic acid; (12S)-12-J2-IsoP[5S,9R]; 5-epi-12-J2-IsoP; 4-((1S,5R)-5-((S,1E,5Z)-3-hydroxyundeca-1,5-dien-1-yl)-4-oxocyclopent-2-en-1-yl)butanoic acid; ent-5,12-diepi-12-J2-IsoP; (12S)-12-J2-IsoP[5R,9S]; 4-((1S,5R)-5-((R,1E,5Z)-3-hydroxyundeca-1,5-dien-1-yl)-4-oxocyclopent-2-en-1-yl)butanoic acid; (12R)-12-J2-IsoP[5R,9S]; ent-5-epi-12-J2-IsoP; (R,5Z,9E)-8-hydroxy-10-((1S,5S)-2-oxo-5-pentylcyclopent-3-en-1-yl)deca-5,9-dienoic acid; (8R)-8-A2-IsoP[11S,15S]; ent-8-A2-IsoP; (S,5Z,9E)-8-hydroxy-10-((1S,5S)-2-oxo-5-pentylcyclopent-3-en-1-yl)deca-5,9-dienoic acid; (8S)-8-A2-IsoP[11S,15S]; ent-8-epi-8-A2-IsoP; (S,5Z,9E)-8-hydroxy-10-((1R,5S)-2-oxo-5-pentylcyclopent-3-en-1-yl)deca-5,9-dienoic acid; ent-8,11-diepi-8-A2-IsoP; (8S)-8-A2-IsoP[11R,15S]; (R,5Z,9E)-8-hydroxy-10-((1R,5S)-2-oxo-5-pentylcyclopent-3-en-1-yl)deca-5,9-dienoic acid; (8R)-8-A2-IsoP[11R,15S]; ent-11-epi-8-A2-IsoP; (R,5Z,9E)-8-hydroxy-10-((1R,5R)-2-oxo-5-pentylcyclopent-3-en-1-yl)deca-5,9-dienoic acid; (8R)-8-A2-IsoP[11R,15R]; 8-epi-8-A2-IsoP; (R,5Z,9E)-8-hydroxy-10-((1S,5R)-2-oxo-5-pentylcyclopent-3-en-1-yl)deca-5,9-dienoic acid; (8R)-8-A2-IsoP[11S,15R]; 8,11-diepi-8-A2-IsoP; (S,5Z,9E)-8-hydroxy-10-((1S,5R)-2-oxo-5-pentylcyclopent-3-en-1-yl)deca-5,9-dienoic acid; 11-epi-8-A2-IsoP; 5S-hydroxy-9-oxo-6E,10,14Z-prostatrienoic acid-cyclo[8R,12S]; (5S)-5-A2-IsoP[8R,12S]; ent-8-epi-5-A2-IsoP; (R,E)-5-hydroxy-7-((1S,2S)-2-((Z)-oct-2-en-1-yl)-5-oxocyclopent-3-en-1-yl)hept-6-enoic acid; (5R)-5-A2-IsoP[8S,12S]; ent-5-A2-IsoP; (S,E)-5-hydroxy-7-((1S,2S)-2-((Z)-oct-2-en-1-yl)-5-oxocyclopent-3-en-1-yl)hept-6-enoic acid; (5S)-5-A2-IsoP[8S,12S]; ent-5-epi-5-A2-IsoP; (S,E)-5-hydroxy-7-((1R,2S)-2-((Z)-oct-2-en-1-yl)-5-oxocyclopent-3-en-1-yl)hept-6-enoic acid; ent-5,8-diepi-5-A2-IsoP; 5S-hydroxy-9-oxo-6E,10,14Z-prostatrienoic acid-cyclo[8S,12R]; (5S)-5-A2-IsoP[8S,12R]; 8-epi-5-A2-IsoP; (R,E)-5-hydroxy-7-((1R,2R)-2-((Z)-oct-2-en-1-yl)-5-oxocyclopent-3-en-1-yl)hept-6-enoic acid; (5R)-5-A2-IsoP[8R,12R]; 5-epi-5-A2-IsoP; (R,E)-5-hydroxy-7-((1S,2R)-2-((Z)-oct-2-en-1-yl)-5-oxocyclopent-3-en-1-yl)hept-6-enoic acid; (5R)-5-A2-IsoP[8S,12R]; 5,8-diepi-5-A2-IsoP; 4-((1R,2S)-2-((R,1E,5Z)-3-hydroxyundeca-1,5-dien-1-yl)-5-oxocyclopent-3-en-1-yl)butanoic acid; (12R)-12-A2-IsoP[5R,9S]; ent-5-epi-12-A2-IsoP; 4-((1R,2S)-2-((S,1E,5Z)-3-hydroxyundeca-1,5-dien-1-yl)-5-oxocyclopent-3-en-1-yl)butanoic acid; ent-5,12-diepi-12-A2-IsoP; (12S)-12-A2-IsoP[5R,9S]; 4-((1S,2S)-2-((R,1E,5Z)-3-hydroxyundeca-1,5-dien-1-yl)-5-oxocyclopent-3-en-1-yl)butanoic acid; (12R)-12-A2-IsoP[5S,9S]; ent-12-A2-IsoP; 4-((1S,2S)-2-((S,1E,5Z)-3-hydroxyundeca-1,5-dien-1-yl)-5-oxocyclopent-3-en-1-yl)butanoic acid; (12S)-12-A2-IsoP[5S,9S]; ent-12-epi-12-A2-IsoP; 4-((1S,2R)-2-((S,1E,5Z)-3-hydroxyundeca-1,5-dien-1-yl)-5-oxocyclopent-3-en-1-yl)butanoic acid; (12S)-12-A2-IsoP[5S,9R]; 5-epi-12-A2-IsoP; 4-((1S,2R)-2-((R,1E,5Z)-3-hydroxyundeca-1,5-dien-1-yl)-5-oxocyclopent-3-en-1-yl)butanoic acid; (12R)-12-A2-IsoP[5S,9R]; 5,12-diepi-12-A2-IsoP; 4-((1R,2R)-2-((R,1E,5Z)-3-hydroxyundeca-1,5-dien-1-yl)-5-oxocyclopent-3-en-1-yl)butanoic acid; (12R)-12-A2-IsoP[5R,9R]; 12-epi-12-A2-IsoP; 9-oxo-15R-hydroxy-5Z,10,13E-prostatrienoic acid-cyclo[8S,12R]; (15R)-15-A2-IsoP[8S,12R]; 8,15-diepi-15-A2-IsoP; 9-oxo-15S-hydroxy-5Z,10,13E-prostatrienoic acid-cyclo[8S,12R]; (15S)-15-A2-IsoP[8S,12R]; 8-epi-15-A2-IsoP; 9-oxo-15S-hydroxy-5Z,10,13E-prostatrienoic acid-cyclo[8S,12S]; (15S)-15-A2-IsoP[8S,12S]; ent-15-epi-15-A2-IsoP; 9-oxo-15R-hydroxy-5Z,10,13E-prostatrienoic acid-cyclo[8R,12R]; (15R)-15-A2-IsoP[8R,12R]; 15-epi-15-A2-IsoP; 9-oxo-15S-hydroxy-5Z,10,13E-prostatrienoic acid-cyclo[8R,12R]; (15S)-15-A2-IsoP[8R,12R]; 15-A2-IsoP; 9-oxo-15R-hydroxy-5Z,10,13E-prostatrienoic acid-cyclo[8S,12S]; (15R)-15-A2-IsoP[8S,12S]; ent-15-A2-IsoP; 11-oxo-15R-hydroxy-5Z,9,13E-prostatrienoic acid-cyclo[8R,12S]; (15R)-15-J2-IsoP[8R,12S]; 8,15-diepi-15-J2c-IsoP; 11-oxo-15R-hydroxy-5Z,9,13E-prostatrienoic acid-cyclo[8S,12R]; (15R)-15-J2-IsoP[8S,12R]; 8,15-diepi-15-J2t-IsoP; 11-oxo-15S-hydroxy-5Z,9,13E-prostatrienoic acid-cyclo[8R,12S]; (15S)-15-J2-IsoP[8R,12S]; 8-epi-15-J2-IsoP; 15S-hydroxy-11-oxo-5Z,9,13E-prostatrienoic acid-cyclo[8R,12R]; (15S)-15-J2-IsoP[8R,12R]; ent-15-epi-15-J2-IsoP; 15R-hydroxy-11-oxo-5Z,9,13E-prostatrienoic acid-cyclo[8S,12S]; (15R)-15-J2-IsoP[8S,12S]; 15-epi-15-J2-IsoP; 15R-hydroxy-11-oxo-5Z,9,13E-prostatrienoic acid-cyclo[8R,12R]; (15R)-15-J2-IsoP[8R,12R]; ent-15-J2-IsoP; 12S-hydroxy-8-oxo-6,10E,14Z-prostatrienoic acid-cyclo[5R,9R]; (12S)-12-J2-IsoP[5R,9R]; ent-12-epi-12-J2-IsoP; 12R-hydroxy-8-oxo-6,10E,14Z-prostatrienoic acid-cyclo[5S,9S]; (12R)-12-J2-IsoP[5S,9S]; 12-epi-12-J2-IsoP; 12S-hydroxy-8-oxo-6,10E,14Z-prostatrienoic acid-cyclo[5S,9S]; (12S)-12-J2-IsoP[5S,9S]; 12-J2-IsoP; 12R-hydroxy-8-oxo-6,10E,14Z-prostatrienoic acid-cyclo[5R,9R]; (12R)-12-J2-IsoP[5R,9R]; ent-12-J2-IsoP; 5S-hydroxy-11-oxo-6E,14Z,12-prostatrienoic acid-cyclo[8S,12R]; (5S)-5-J2-IsoP[8S,12R]; ent-5-epi-5-J2-IsoP; 5R-hydroxy-11-oxo-6E,14Z,12-prostatrienoic acid-cyclo[8R,12S]; (5R)-5-J2-IsoP[8R,12S]; 5-epi-5-J2-IsoP; 5R-hydroxy-11-oxo-6E,14Z,12-prostatrienoic acid-cyclo[8S,12R]; (5R)-5-J2-IsoP[8S,12R]; ent-5-J2-IsoP; 8S-hydroxy-14-oxo-5Z,9E,12-prostatrienoic acid-cyclo[11S,15R]; (8S)-8-J2-IsoP[11S,15R]; ent-8-epi-8-J2-IsoP; 8R-hydroxy-14-oxo-5Z,9E,12-prostatrienoic acid-cyclo[11R,15S]; (8R)-8-J2-IsoP[11R,15S]; 8-epi-8-J2-IsoP; 8R-hydroxy-14-oxo-5Z,9E,12-prostatrienoic acid-cyclo[11S,15R]; (8R)-8-J2-IsoP[11S,15R]; ent-8-J2-IsoP; 9S,15S-dihydroxy-5Z,7E,11Z,13E,17Z-eicosapentaenoic acid; 9,15-diHEPE; 12R,13R-dihydroxy-eicosa-5Z,8Z,10E,14Z,17Z-pentaenoic acid; 8,18-dihydroxy-5Z,9E,11Z,14Z,16E-eicosapentaenoic acid; 8,18-di-HEPE; 12,18-dihydroxy-5Z,8Z,10E,14Z,16E-eicosapentaenoic acid; 12,18-di-HEPE; 11,18-dihydroxy-5Z,8Z,12E,14Z,16E-eicosapentaenoic acid; 11,18-di-HEPE; 14,15-epoxy-13-hydroxy-5Z,8Z,11Z,17Z-eicosatetraenoic acid; 14,15-epoxy,13-HETE; 13,14-HepETE; 14,15-epoxy-16-hydroxy-5Z,8Z,11Z,17Z-eicosapentaenoic acid; 14,15-epoxy,16-HETE; 16,14-HepETE; (6E,8E,10E,12R,14Z)-12-hydroxy-5-oxoicosa-6,8,10,14-tetraenoic acid; 5-Oxo-6-trans-leukotriene B4; 5S-hydroxy-12-keto-6Z,8E,10E,14Z-eicosatetraenoic acid; 12-oxo-Leukotriene B4; 12-Oxo-ltb4; 5S,12R-dihydroxy-6Z,8E,10E-eicosatriene-14-ynoic acid; 14,15-dehydro-Leukotriene B4; 14,15-dehydro-LTB4; 9-oxo-11R-hydroxy-5Z,13E-prostadienoic acid-1,15S-lactone; Prostaglandin E2 1,15-lactone; PGE2 1,15-lactone; 9S,11R-dihydroxy-5Z,13E,17Z-prostatrienoic acid-1,15S-lactone; Prostaglandin F3alpha-1,15-lactone; PGF3alpha-1,15-lactone; 9oxo-15S-hydroxy-5E,10Z,13E-prostatrienoic acid; 5-trans-Prostaglandin A2; 5-trans-PGA2; 9S-hydroxy-11-oxo-5Z,12E,14E-prostatrienoic acid; 15-deoxy-delta-12,14-Prostaglandin D2; 15-deoxy-delta-12,14-PGD2; 15-deoxy-PGD2; 13,14-dihydro-15-keto-Prostaglandin A2; 9,15-dioxo-5Z,10-prostadienoic acid; 13,14-dihydro-15-keto-PGA2; 11-oxo-15S-hydroxy-5Z,9Z,13E-prostatrienoic acid; delta-12-Prostaglandin J2; delta-12-PGJ2; 5Z,8Z,11Z,14Z-Eicosatetraenedioic acid



数据库引用编号

177 个数据库交叉引用编号

分类词条

相关代谢途径

Reactome(5)

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)

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

  • Xiang Fang, Joseph S Dillon, Shanming Hu, Shawn D Harmon, Jianrong Yao, Siddam Anjaiah, J R Falck, Arthur A Spector. 20-carboxy-arachidonic acid is a dual activator of peroxisome proliferator-activated receptors alpha and gamma. Prostaglandins & other lipid mediators. 2007 Jan; 82(1-4):175-84. doi: 10.1016/j.prostaglandins.2006.05.002. [PMID: 17164145]
  • Wolfgang Neuhofer, Konstantin Holzapfel, Maria-Luisa Fraek, Nengtai Ouyang, Jens Lutz, Franz-X Beck. Chronic COX-2 inhibition reduces medullary HSP70 expression and induces papillary apoptosis in dehydrated rats. Kidney international. 2004 Feb; 65(2):431-41. doi: 10.1111/j.1523-1755.2004.00387.x. [PMID: 14717913]
  • Akos Heinemann, Rufina Schuligoi, Ian Sabroe, Adele Hartnell, Bernhard A Peskar. Delta 12-prostaglandin J2, a plasma metabolite of prostaglandin D2, causes eosinophil mobilization from the bone marrow and primes eosinophils for chemotaxis. Journal of immunology (Baltimore, Md. : 1950). 2003 May; 170(9):4752-8. doi: 10.4049/jimmunol.170.9.4752. [PMID: 12707356]
  • E F Mc Clay. The effects of Delta(12)-PGJ(2) on malignant cells. Prostaglandins & other lipid mediators. 2000 Jun; 62(1):75-90. doi: 10.1016/s0090-6980(00)00076-9. [PMID: 10936416]
  • K W Marvin, R L Eykholt, J A Keelan, T A Sato, M D Mitchell. The 15-deoxy-delta(12,14)-prostaglandin J(2)receptor, peroxisome proliferator activated receptor-gamma (PPARgamma) is expressed in human gestational tissues and is functionally active in JEG3 choriocarcinoma cells. Placenta. 2000 May; 21(4):436-40. doi: 10.1053/plac.1999.0485. [PMID: 10833383]
  • D H Wright, K M Metters, M Abramovitz, A W Ford-Hutchinson. Characterization of the recombinant human prostanoid DP receptor and identification of L-644,698, a novel selective DP agonist. British journal of pharmacology. 1998 Apr; 123(7):1317-24. doi: 10.1038/sj.bjp.0701708. [PMID: 9579725]
  • S Fukushima, S Kishimoto, Y Takeuchi, M Fukushima, M Suzuki, K Furuta, R Noyori, H Sasaki, Y Kikuchi, M Nakano, S Kurozumi. [Pharmaceutical and pharmacological development of antitumor prostaglandins]. Nihon rinsho. Japanese journal of clinical medicine. 1998 Mar; 56(3):663-9. doi: . [PMID: 9549353]
  • T Yokomizo, T Izumi, T Takahashi, T Kasama, Y Kobayashi, F Sato, Y Taketani, T Shimizu. Enzymatic inactivation of leukotriene B4 by a novel enzyme found in the porcine kidney. Purification and properties of leukotriene B4 12-hydroxydehydrogenase. The Journal of biological chemistry. 1993 Aug; 268(24):18128-35. doi: . [PMID: 8394361]
  • C Amici, A T Palamara, E Garaci, M G Santoro. Inhibition of Sendai virus replication by delta 12-prostaglandin J2: induction of heat shock protein synthesis and alteration of protein glycosylation. Antiviral research. 1992 Aug; 19(2):129-38. doi: 10.1016/0166-3542(92)90072-d. [PMID: 1332600]
  • M A Carroll, M P Garcia, J R Falck, J C McGiff. Cyclooxygenase dependency of the renovascular actions of cytochrome P450-derived arachidonate metabolites. The Journal of pharmacology and experimental therapeutics. 1992 Jan; 260(1):104-9. doi: . [PMID: 1731035]
  • G Nishimura. [Antitumor activity and cell cycle effects of delta 12-PGJ2 in vivo]. Nihon Gan Chiryo Gakkai shi. 1990 Mar; 25(3):632-9. doi: . [PMID: 2351856]
  • Y Kikawa, S Narumiya, M Fukushima, H Wakatsuka, O Hayaishi. 9-Deoxy-delta 9, delta 12-13,14-dihydroprostaglandin D2, a metabolite of prostaglandin D2 formed in human plasma. Proceedings of the National Academy of Sciences of the United States of America. 1984 Mar; 81(5):1317-21. doi: 10.1073/pnas.81.5.1317. [PMID: 6584883]