Methyl dodecanoate (BioDeep_00000017681)

 

Secondary id: BioDeep_00000616651

human metabolite PANOMIX_OTCML-2023 Endogenous


代谢物信息卡片


Methyl laurate, United States Pharmacopeia (USP) Reference Standard

化学式: C13H26O2 (214.1932696)
中文名称: 月桂酸甲酯
谱图信息: 最多检出来源 Chinese Herbal Medicine(otcml) 1.63%

分子结构信息

SMILES: CCCCCCCCCCCC(=O)OC
InChI: InChI=1S/C13H26O2/c1-3-4-5-6-7-8-9-10-11-12-13(14)15-2/h3-12H2,1-2H3

描述信息

Methyl laurate is a fatty acid methyl ester of lauric acid. It has a role as a metabolite. It is a fatty acid methyl ester and a dodecanoate ester.
Methyl dodecanoate is a natural product found in Astragalus mongholicus, Cocos nucifera, and other organisms with data available.
Methyl dodecanoate is found in alcoholic beverages. Methyl dodecanoate is found in concord grape (Vitis labrusca), melon, pineapple, heated blackberry, red chilli (Capsicum frutescens) and other fruits. Also present in cheeses, hop oil, white wine, spirits and other foodstuffs. Methyl dodecanoate is a flavouring agent. Methyl dodecanoate belongs to the family of Fatty Acid Esters. These are carboxylic ester derivatives of a fatty acid.
Methyl dodecanoate is found in alcoholic beverages. Methyl dodecanoate is found in concord grape (Vitis labrusca), melon, pineapple, heated blackberry, red chilli (Capsicum frutescens) and other fruits. Also present in cheeses, hop oil, white wine, spirits and other foodstuffs. Methyl dodecanoate is a flavouring agent
Found in concord grape (Vitis labrusca), melon, pineapple, heated blackberry, red chilli (Capsicum frutescens) and other fruitsand is also present in cheeses, hop oil, white wine, spirits and other foodstuffs. Flavouring agent.
A fatty acid methyl ester of lauric acid.
Methyl laurate, a 12-carbon saturated fatty acid, is an esterified version of lauric acid[1].
Methyl laurate, a 12-carbon saturated fatty acid, is an esterified version of lauric acid[1].

同义名列表

45 个代谢物同义名

Methyl laurate, United States Pharmacopeia (USP) Reference Standard; Methyl laurate, certified reference material, TraceCERT(R); 4-02-00-01090 (Beilstein Handbook Reference); Methyl dodecanoate, analytical standard; Dodecanoic acid methyl ester (FAME MIX); lauric acid methyl ester, C14-labeled; Methyl laurate, natural, 98\\%, FG; Dodecanoic acid, methyl ester; dodecanoic acid methyl ester; dodecanoic acid-methyl ester; Methyl laurate, >=98\\%, FG; METHYL DODECANOATE, 99.8\\%; Lauric acid, methyl ester; METHYL DODECANOATE [HSDB]; Methyl N-dodecanoic acid; lauric acid methyl ester; METHYL LAURATE [USP-RS]; Methyl laurate, 99.5\\%; Laic acid methyl ester; Methyl dodecanoic acid; Methyl dodecylic acid; METHYL LAURATE [INCI]; METHYL LAURATE [FHFI]; Methyl n-dodecanoate; Methyl laurinic acid; METHYL LAURATE [II]; Methyl dodecanoate; Laate methyl ester; Uniphat A40 IN 511; Methyl dodecylate; Methyl laurinate; UNII-8IPS6BI6KW; Methyl-Laurate; Metholene 2296; Methyl laurate; Tox21_201488; WE(1:0/12:0); Tox21_300555; Uniphat A40; 8IPS6BI6KW; Stepan C40; FEMA 2715; AI3-00669; SFE 13:0; C12 FAME



数据库引用编号

15 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)

12 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

  • Takao Roppongi, Naho Mizuno, Yayoi Miyagawa, Takashi Kobayashi, Kyuya Nakagawa, Shuji Adachi. Solubility and mass transfer coefficient of oxygen through gas- and water-lipid interfaces. Journal of food science. 2021 Mar; 86(3):867-873. doi: 10.1111/1750-3841.15641. [PMID: 33580513]
  • Herny Ei Simbala, Edwin De Queljoe, Max Rj Runtuwene, Trina Ekawati Tallei. Bioactive compounds in Pinang Yaki (Areca vestiaria) fruit as potential source of antifertility agent. Pakistan journal of pharmaceutical sciences. 2017 Sep; 30(5(Supplementary)):1929-1937. doi: ". [PMID: 29105623]
  • Eriko Harada, Jun Nakagawa, Tsunaki Asano, Masato Taoka, Hiroyuki Sorimachi, Yoshihiro Ito, Toshiro Aigaki, Takashi Matsuo. Functional evolution of duplicated odorant-binding protein genes, Obp57d and Obp57e, in Drosophila. PloS one. 2012; 7(1):e29710. doi: 10.1371/journal.pone.0029710. [PMID: 22238638]
  • Abderrahim Bouaid, Mercedes Martínez, José Aracil. Biorefinery approach for coconut oil valorisation: a statistical study. Bioresource technology. 2010 Jun; 101(11):4006-12. doi: 10.1016/j.biortech.2009.12.074. [PMID: 20129777]
  • Anh N Hoang, Kanyile K Ncokazi, Katherine A de Villiers, David W Wright, Timothy J Egan. Crystallization of synthetic haemozoin (beta-haematin) nucleated at the surface of lipid particles. Dalton transactions (Cambridge, England : 2003). 2010 Feb; 39(5):1235-44. doi: 10.1039/b914359a. [PMID: 20104349]
  • Gretel Mara Hunzicker. A novel regulatory system in plants involving medium-chain fatty acids. Planta. 2009 Dec; 231(1):143-53. doi: 10.1007/s00425-009-1032-1. [PMID: 19876644]
  • Dapeng Li, Jin Shen, Tao Wu, Yunfeng Xu, Xiaojuan Zong, Dequan Li, Huairui Shu. Overexpression of the apple alcohol acyltransferase gene alters the profile of volatile blends in transgenic tobacco leaves. Physiologia plantarum. 2008 Nov; 134(3):394-402. doi: 10.1111/j.1399-3054.2008.01152.x. [PMID: 18636987]
  • Muhammad Ishtiaq Ch, Yang F Wen, YiYu Cheng. Gas chromatographic/mass spectrometric analysis of the essential oil of Houttuynia cordata Thunb by using on-column methylation with tetramethylammonium acetate. Journal of AOAC International. 2007 Jan; 90(1):60-7. doi: . [PMID: 17373437]
  • Lalatendu Panigrahi, Snigdha Pattnaik, Saroj K Ghosal. The effect of pH and organic ester penetration enhancers on skin permeation kinetics of terbutaline sulfate from pseudolatex-type transdermal delivery systems through mouse and human cadaver skins. AAPS PharmSciTech. 2005 Sep; 6(2):E167-73. doi: 10.1208/pt060225. [PMID: 16353974]