Diethyl succinate (BioDeep_00000017739)

 

Secondary id: BioDeep_00000618715, BioDeep_00000869288

human metabolite PANOMIX_OTCML-2023 Endogenous


代谢物信息卡片


InChI=1/C8H14O4/c1-3-11-7(9)5-6-8(10)12-4-2/h3-6H2,1-2H

化学式: C8H14O4 (174.0892044)
中文名称: 琥珀酸二乙酯, 丁二酸二乙酯
谱图信息: 最多检出来源 Chinese Herbal Medicine(otcml) 3.13%

分子结构信息

SMILES: CCOC(=O)CCC(=O)OCC
InChI: InChI=1S/C8H14O4/c1-3-11-7(9)5-6-8(10)12-4-2/h3-6H2,1-2H3

描述信息

Diethyl succinate is a fatty acid ester.
Diethyl succinate is a natural product found in Mimusops elengi, Opuntia ficus-indica, and other organisms with data available.
Diethyl butanedioate is a metabolite found in or produced by Saccharomyces cerevisiae.
Diethyl succinate, also known as diethyl butanedioate, belongs to the class of organic compounds known as fatty acid esters. These are carboxylic ester derivatives from a fatty acid.
Flavour ingredient

同义名列表

35 个代谢物同义名

InChI=1/C8H14O4/c1-3-11-7(9)5-6-8(10)12-4-2/h3-6H2,1-2H; Diethyl succinate, Vetec(TM) reagent grade, 98\\%; 4-02-00-01914 (Beilstein Handbook Reference); Diethyl succinate, ReagentPlus(R), 99\\%; Diethylester kyseliny jantarove [Czech]; Diethyl succinate, natural, >=99\\%, FG; Diethyl succinate, analytical standard; Butanedioic acid, 1,4-diethyl ester; Diethyl succinate, >=99\\%, FCC, FG; Diethyl ester of butanedioic acid; SUCCINIC ACID DIETHYL ESTER [MI]; Diethylester kyseliny jantarove; Butanedioic acid, diethyl ester; butanedioic acid diethyl ester; 1,4-Diethyl butanedioic acid; Succinic acid, diethyl ester; Succinic acid-diethyl ester; Diethyl ethanedicarboxylate; Succinic acid diethyl ester; DIETHYL SUCCINATE [FHFI]; DIETHYL SUCCINATE [INCI]; 1,4-diethyl butanedioate; Diethyl succinate, 98\\%; DIETHYL SUCCINATE [FCC]; Diethyl succinic acid; Diethyl butanedioate; Diethyl butanoate; Diethyl succinate; DIETHYLSUCCINATE; UNII-ELP55C13DR; Ethyl succinate; Tox21_300286; WLN: 2OV2VO2; ELP55C13DR; AI3-00682



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)

3 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

  • Alvaro Orjuela, Andrea Orjuela, Carl T Lira, Dennis J Miller. A novel process for recovery of fermentation-derived succinic acid: process design and economic analysis. Bioresource technology. 2013 Jul; 139(?):235-41. doi: 10.1016/j.biortech.2013.03.174. [PMID: 23665683]
  • Zuoshan Feng, Yujia Bai, Fanglin Lu, Wenshu Huang, Xinmin Li, Xiaosong Hu. Effect of asafoetida extract on growth and quality of Pleurotus ferulic. International journal of molecular sciences. 2009 Dec; 11(1):41-51. doi: 10.3390/ijms11010041. [PMID: 20162000]
  • Koichi Takahashi, Hitomi Sakano, Nanako Numata, Shiho Kuroda, Nobuyasu Mizuno. Effect of fatty acid diesters on permeation of anti-inflammatory drugs through rat skin. Drug development and industrial pharmacy. 2002 Nov; 28(10):1285-94. doi: 10.1081/ddc-120015362. [PMID: 12476874]
  • M B Ashour, D E Moody, B D Hammock. Apparent induction of microsomal carboxylesterase activities in tissues of clofibrate-fed mice and rats. Toxicology and applied pharmacology. 1987 Jul; 89(3):361-9. doi: 10.1016/0041-008x(87)90155-4. [PMID: 3603566]