Methyl Arachidonate (BioDeep_00000018231)

   

human metabolite Endogenous natural product


代谢物信息卡片


(5Z,8Z,11Z,14Z)-Methyl icosa-5,8,11,14-tetraenoate

化学式: C21H34O2 (318.2559)
中文名称: 花生四烯酸甲酯
谱图信息: 最多检出来源 Homo sapiens(not specific) 50%

分子结构信息

SMILES: CCCCC/C=C\C/C=C\C/C=C\C/C=C\CCCC(=O)OC
InChI: InChI=1S/C21H34O2/c1-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20-21(22)23-2/h7-8,10-11,13-14,16-17H,3-6,9,12,15,18-20H2,1-2H3/b8-7-,11-10-,14-13?,17-16-

描述信息

Methyl Arachidonate, also known as Arachidonate methyl ester or (5Z,8Z,11Z,14Z)-Icosatetraenoate methyl ester, is classified as a member of the Fatty acid methyl esters. Fatty acid methyl esters are compounds containing a fatty acid that is esterified with a methyl group. They have the general structure RC(=O)OR, where R=fatty aliphatic tail or organyl group and R=methyl group. Methyl Arachidonate is considered to be practically insoluble (in water) and basic. Methyl Arachidonate can be synthesized from arachidonic acid. Methyl Arachidonate can be synthesized into 12(R)-HPETE methyl ester and 12(S)-HPETE methyl ester

同义名列表

15 个代谢物同义名

(5Z,8Z,11Z,14Z)-Methyl icosa-5,8,11,14-tetraenoate; (5Z,8Z,11Z,14Z)-Icosatetraenoic acid methyl ester; Methyl (5Z,8Z,11Z,14Z)-5,8,11,14-icosatetraenoate; 1-O-Methyl (5Z,8Z,11Z,14Z)-eicosatetraenoic acid; methyl (5Z,11Z,14Z)-icosa-5,8,11,14-tetraenoate; Methyl all-cis-5,8,11,14-eicosatetraenoic acid; (5Z,8Z,11Z,14Z)-Icosatetraenoate methyl ester; 1-O-Methyl (5Z,8Z,11Z,14Z)-eicosatetraenoate; Methyl (5Z)-icosa-5,8,11,14-tetraenoic acid; Methyl all-cis-5,8,11,14-eicosatetraenoate; Arachidonic acid methyl ester; Arachidonate methyl ester; Methyl arachidonic acid; Methyl arachidonate; Methyl arachidonate



数据库引用编号

6 个数据库交叉引用编号

分类词条

相关代谢途径

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代谢反应

0 个相关的代谢反应过程信息。

Reactome(0)

BioCyc(0)

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Plant Reactome(0)

INOH(0)

PlantCyc(0)

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PharmGKB(0)

48 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。

亚细胞结构定位 关联基因列表


文献列表

  • Ekaterina A Placzek, Bruce R Cooper, Andrew T Placzek, Julia A Chester, V Jo Davisson, Eric L Barker. Lipidomic metabolism analysis of the endogenous cannabinoid anandamide (N-arachidonylethanolamide). Journal of pharmaceutical and biomedical analysis. 2010 Nov; 53(3):567-75. doi: 10.1016/j.jpba.2010.03.035. [PMID: 20417049]
  • Atnan Uğur, Ipek Süntar, Sinem Aslan, Ilkay Erdoğan Orhan, Murat Kartal, Nazim Sekeroğlu, Dursun Eşiyok, Bilge Sener. Variations in fatty acid compositions of the seed oil of Eruca sativa Mill. caused by different sowing periods and nitrogen forms. Pharmacognosy magazine. 2010 Oct; 6(24):305-8. doi: 10.4103/0973-1296.71801. [PMID: 21120033]
  • Carla Ferreri, Dimitris Anagnostopoulos, Ioannis N Lykakis, Chryssostomos Chatgilialoglu, Athanassia Siafaka-Kapadai. Synthesis of all-trans anandamide: a substrate for fatty acid amide hydrolase with dual effects on rabbit platelet activation. Bioorganic & medicinal chemistry. 2008 Sep; 16(18):8359-65. doi: 10.1016/j.bmc.2008.08.054. [PMID: 18782671]
  • Ross M Taylor, Thomas R Foubert, James B Burritt, Danas Baniulis, Linda C McPhail, Algirdas J Jesaitis. Anionic amphiphile and phospholipid-induced conformational changes in human neutrophil flavocytochrome b observed by fluorescence resonance energy transfer. Biochimica et biophysica acta. 2004 May; 1663(1-2):201-13. doi: 10.1016/j.bbamem.2004.03.009. [PMID: 15157622]
  • Carla Ferreri, M Rosaria Faraone Mennella, Cesare Formisano, Laura Landi, Chryssostomos Chatgilialoglu. Arachidonate geometrical isomers generated by thiyl radicals: the relationship with trans lipids detected in biological samples. Free radical biology & medicine. 2002 Dec; 33(11):1516-26. doi: 10.1016/s0891-5849(02)01083-3. [PMID: 12446209]
  • H Sprinz, S Adhikari, O Brede. Transformation of phospholipid membranes by thiyl radicals via cis-trans isomerization of fatty acid residues. Advances in colloid and interface science. 2001 Jan; 89-90(?):313-25. doi: 10.1016/s0001-8686(00)00063-4. [PMID: 11215801]