DL-Dopa (BioDeep_00000027616)

Main id: BioDeep_00000000461

 

human metabolite PANOMIX_OTCML-2023 Endogenous blood metabolite BioNovoGene_Lab2019


代谢物信息卡片


alpha-amino-3,4-Dihydroxy-benzenepropanoic acid

化学式: C9H11NO4 (197.0688046)
中文名称: 3-(3,4-二羟苯基)-DL-丙氨酸, DL-二羟基苯丙氨酸
谱图信息: 最多检出来源 () 0%

分子结构信息

SMILES: NC(CC1=CC=C(O)C(O)=C1)C(O)=O
InChI: InChI=1S/C9H11NO4/c10-6(9(13)14)3-5-1-2-7(11)8(12)4-5/h1-2,4,6,11-12H,3,10H2,(H,13,14)

描述信息

DL-DOPA, also known as (+-)-DOPA or (R,S)-DOPA or DL-3,4-dihydroxyphenylalanine is an alpha amino acid. These are amino acids in which the amino group is attached to the carbon atom immediately adjacent to the carboxylate group (alpha carbon). DL-DOPA also belongs to the class of organic compounds known as tyrosines and derivatives. Tyrosines and derivatives are compounds containing tyrosine or a derivative thereof resulting from reaction of tyrosine at the amino group or the carboxy group, or from the replacement of any hydrogen of glycine by a heteroatom. DL-DOPA is a racemic mixture of both D-DOPA and L-DOPA. D-DOPA is similar to L-DOPA (levodopa), but with opposite chirality. Levo- and dextro- rotation refer to a molecules ability to rotate planes of polarized light in one or the other direction. Whereas L-DOPA is moderately effective in the treatment of Parkinsons disease (PD) by stimulating the production of dopamine in the brain, D-DOPA was at one time thought to be biologically inactive. However, it has recently been found that D-DOPA can be converted to L-DOPA and then to dopamine via the human enzyme known as D-amino acid oxidase and that racemic mixtures of DL-DOPA can be effective in treating Parkinsonism (PMID: 17924443; PMID: 3129126; PMID: 17042912). The biological production or biosynthesis of D-DOPA is thought to occur through bacterial conversion of tyrosine. L-DOPA is found naturally in both animals and plants. It is made via biosynthesis from the amino acid L-tyrosine by the enzyme tyrosine hydroxylase. L-DOPA is the precursor to the neurotransmitters dopamine, norepinephrine (noradrenaline), and epinephrine (adrenaline), which are collectively known as catecholamines.
The naturally occurring form of DIHYDROXYPHENYLALANINE and the immediate precursor of DOPAMINE. Unlike dopamine itself, it can be taken orally and crosses the blood-brain barrier. It is rapidly taken up by dopaminergic neurons and converted to DOPAMINE. It is used for the treatment of PARKINSONIAN DISORDERS and is usually given with agents that inhibit its conversion to dopamine outside of the central nervous system. [HMDB]
DL-Dopa is a beta-hydroxylated derivative of phenylalanine.
DL-Dopa is a beta-hydroxylated derivative of phenylalanine.

同义名列表

41 个代谢物同义名

alpha-amino-3,4-Dihydroxy-benzenepropanoic acid; 2-amino-3-(3,4-Dihydroxyphenyl)propanoic acid; alpha-amino-3,4-Dihydroxy-benzenepropanoate; beta-(3,4-Dihydroxyphenyl)-DL-alpha-alanine; Dihydroxyphenylalanine hydrochloride, (2:1); DL-beta-(3,4-Dihydroxyphenyl)-alpha-alanine; a-amino-3,4-Dihydroxy-benzenepropanoic acid; 2-amino-3-(3,4-Dihydroxyphenyl)propanoate; beta-(3,4-Dihydroxyphenyl)-alpha-alanine; a-amino-3,4-Dihydroxy-benzenepropanoate; (+/-) 3-(3,4-dihydroxyphenyl)alanine; Β-(3,4-dihydroxyphenyl)-DL-α-alanine; DL-beta-(3,4-Dihydroxyphenyl)alanine; DL-b-(3,4-Dihydroxyphenyl)-a-alanine; DL-Β-(3,4-dihydroxyphenyl)-α-alanine; b-(3,4-Dihydroxyphenyl)-DL-a-alanine; (+-)-3-(3,4-Dihydroxyphenyl)alanine; 3-(3,4-Dihydroxyphenyl)-DL-alanine; DL-Β-(3,4-dihydroxyphenyl)alanine; DL-b-(3,4-Dihydroxyphenyl)alanine; b-(3,4-Dihydroxyphenyl)-a-alanine; 3,4-Dihydroxy-DL-phenylalanine; alpha-amino-Hydrocaffeic acid; DL-3,4-Dihydroxyphenylalanine; DL-4,5-Dihydroxyphenylalanine; 3,4-Dihydroxyphenylalanine; 3,4 Dihydroxyphenylalanine; DL-Dihydroxyphenylalanine; dihydroxyphenylalanine; 3-Hydroxy-DL-tyrosine; 3 Hydroxy DL tyrosine; DL-Dioxyphenylalanine; beta Hydroxytyrosine; DL-3-Hydroxytyrosine; beta-Hydroxytyrosine; 3-Hydroxytyrosine; DL-3,4-Dopa; (R,S)-Dopa; (+-)-Dopa; DL-Dopa; Dopa



数据库引用编号

10 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)

WikiPathways(0)

Plant Reactome(0)

INOH(0)

PlantCyc(0)

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2 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。



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