Diethyl malonate (BioDeep_00000018217)

   

human metabolite Endogenous


代谢物信息卡片


Methanedicarboxylic acid, diethyl ester

化学式: C7H12O4 (160.0736)
中文名称: 丙二酸二乙酯
谱图信息: 最多检出来源 Homo sapiens(not specific) 5%

分子结构信息

SMILES: CCOC(=O)CC(=O)OCC
InChI: InChI=1S/C7H12O4/c1-3-10-6(8)5-7(9)11-4-2/h3-5H2,1-2H3

描述信息

Diethyl malonate, also known as dicarbethoxymethane or ethyl propanedioate, belongs to the class of organic compounds known as dicarboxylic acids and derivatives. These are organic compounds containing exactly two carboxylic acid groups. Diethyl malonate is a sweet, apple, and fruity tasting compound. Diethyl malonate has been detected, but not quantified, in a few different foods, such as alcoholic beverages, evergreen blackberries, and fruits. Like other esters, this compound can undergo bromination at the alpha position. Fischer esterification gives diethyl malonate: One of the principal uses of this compound is in the malonic ester synthesis. It occurs naturally in grapes and strawberries as a colourless liquid with an apple-like odour, and is used in perfumes. Malonic acid is a rather simple dicarboxylic acid, with the two carboxyl groups close together. The hydrogen atoms on a carbon adjacent to two carbonyl groups are even more acidic because the carbonyl groups help stabilize the carbanion resulting from the removal of that proton. Like many other esters, this compound can undergo the Claisen ester condensation. This alkylated 1,3-dicarbonyl compound (3) readily undergoes decarboxylation with loss of carbon dioxide, to give a substituted acetic acid, using Sodium ethoxide as the preferred base. The use of aqueous sodium hydroxide may give the base hydrolysis products: sodium malonate and ethanol.
Diethyl malonate is a flavouring ingredient. It is a rather simple dicarboxylic acid, with two carboxyl groups close together in its molecule. In forming diethyl malonate from malonic acid, the hydroxyl group (-OH) on both of the carboxyl groups is replaced by an ethoxy group (-OEt; -OCH2CH3). The methylene group (-CH2-) in the middle of the malonic part of the diethyl malonate molecule is neighboured by two carbonyl groups (-C(=O)-). Diethyl malonate is found in alcoholic beverages such as wines, and in fruits such as guava, melon, concord grape, pineapple, blackberry.

同义名列表

20 个代谢物同义名

Methanedicarboxylic acid, diethyl ester; Propanedioic acid, 1,3-diethyl ester; Propanedioic acid, diethyl ester; 1,3-Diethyl propanedioic acid; Malonic acid, diethyl ester; Malonic acid diethyl ester; Ethyl methanedicarboxylate; Diethyl propanedioate, 9ci; 1,3-diethyl propanedioate; Carbethoxyacetic ester; Diethyl propanedioate; Diethyl malonic acid; Ethyl propanedioate; Dicarbethoxymethane; DIETHYL MALONATE; Diethylmalonate; Ethyl malonate; Malonic ester; FEMA 2375; Diethyl malonate



数据库引用编号

9 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。

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BioCyc(0)

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INOH(0)

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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。

亚细胞结构定位 关联基因列表


文献列表

  • Vangavaragu Jhansi Rani, Raghavendra Aminedi, Kishore Polireddy, Kanala Jagadeeswarareddy. Synthesis and spectral characterization of new bis(2-(pyrimidin-2-yl)ethoxy)alkanes and their pharmacological activity. Archiv der Pharmazie. 2012 Aug; 345(8):663-9. doi: 10.1002/ardp.201200021. [PMID: 22592977]
  • Hak Sung Kim, Kenneth A Jacobson. Synthesis of a novel conformationally locked carbocyclic nucleoside ring system. Organic letters. 2003 May; 5(10):1665-8. doi: 10.1021/ol034326z. [PMID: 12735747]
  • V V Frol'kis, V V Bezrukov, K K Muradyan. [Age-related properties of inductive synthesis of glucose-6-phosphatase, fructose-1,6-diphosphatase, tyrosine aminotransferase and tryptophan pyrrolase in hypothalamus stimulation]. Voprosy meditsinskoi khimii. 1975 Jul; 21(4):400-6. doi: NULL. [PMID: 3019]