D-Malic acid (BioDeep_00000000728)
Secondary id: BioDeep_00000001119, BioDeep_00000400399, BioDeep_00000415844, BioDeep_00000419033
natural product human metabolite PANOMIX_OTCML-2023 Endogenous Volatile Flavor Compounds
代谢物信息卡片
化学式: C4H6O5 (134.0215226)
中文名称: D-(+)-苹果酸
谱图信息:
最多检出来源 Viridiplantae(plant) 0.18%
分子结构信息
SMILES: C(C(C(=O)O)O)C(=O)O
InChI: InChI=1S/C4H6O5/c5-2(4(8)9)1-3(6)7/h2,5H,1H2,(H,6,7)(H,8,9)/t2-/m1/s1
描述信息
(R)-malic acid is an optically active form of malic acid having (R)-configuration. It is a conjugate acid of a (R)-malate(2-). It is an enantiomer of a (S)-malic acid.
(R)-Malate is a metabolite found in or produced by Escherichia coli (strain K12, MG1655).
D-malate is a natural product found in Vaccinium macrocarpon, Pogostemon cablin, and other organisms with data available.
D-Malic acid is found in herbs and spices. This enantiomer of rare occurrence; reported from fruits and leaves of Hibiscus sabdariffa (roselle) although there are many more isolations of malic acid with no opt. rotn. given and some may be of the R-for
An optically active form of malic acid having (R)-configuration.
COVID info from PDB, Protein Data Bank
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Acquisition and generation of the data is financially supported in part by CREST/JST.
D-(+)-Malic acid (D-Malic acid), an active enantiomer of Malic acid, is a competitive inhibitor of L(--)malic acid transport[1].
D-(+)-Malic acid (D-Malic acid), an active enantiomer of Malic acid, is a competitive inhibitor of L(--)malic acid transport[1].
同义名列表
38 个代谢物同义名
(2R)-2-HYDROXYBUTANEDIOIC ACID; 2-HYDROXY-SUCCINIC ACID; D-(+)-Malic acid, unnatural form, >=97.0\\% (T); AAF7D69B-7713-4E35-92ED-EA50BA0FCDCE; BUTANEDIOIC ACID, 2-HYDROXY-, (2R)-; D-Malic acid, analytical standard; Butanedioic acid, hydroxy-, (2R)-; (R)-(+)-2-Hydroxysuccinic acid; (2R)-2-hydroxybutanedioic acid; (R)-2-hydroxybutanedioic acid; Hydroxy-(R)-Butanedioic acid; (r)-(+)-hydroxysuccinic acid; BJEPYKJPYRNKOW-UWTATZPHSA-N; (R)-Hydroxybutanedioic acid; (R)-2-Hydroxysuccinic acid; MALIC ACID D-(+)-FORM [MI]; (R)-2-Hydroxysuccinicacid; (R)-2-Hydroxybutanedioate; D-Hydroxybutanedioic acid; 2-HYDROXY-SUCCINIC ACID; Malic acid D-(+)-form; ApfelsA currencyure; 2-HYDROXY-succinate; Malic acid, L(+)-; D-(+)-Malic acid; D-(+)-Apple Acid; (+)-D-malic acid; D(+)-Malic acid; L(+)-Malic acid; .+-.-Malic acid; (R)-malic acid; Malic acid, D-; (+)-Malic acid; D-malic acid; (+)-D-Malate; R-Malic acid; (R)-malate; D-malate; (R)-Malate
数据库引用编号
26 个数据库交叉引用编号
- ChEBI: CHEBI:30796
- KEGG: C00497
- PubChem: 92824
- HMDB: HMDB0031518
- Metlin: METLIN63096
- DrugBank: DB03499
- ChEMBL: CHEMBL225986
- Wikipedia: Malic_acid
- ChemIDplus: 0000636613
- MetaCyc: CPD-660
- foodb: FDB008115
- chemspider: 83793
- CAS: 636-61-3
- MoNA: PR100541
- MoNA: PS020007
- medchemexpress: HY-20558
- MetaboLights: MTBLC30796
- ChEBI: CHEBI:15588
- PubChem: 3780
- PDB-CCD: MLT
- 3DMET: B01268
- NIKKAJI: J14.674I
- RefMet: D-Malic acid
- LOTUS: LTS0237082
- wikidata: Q27104149
- KNApSAcK: 15588
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)
8 个相关的物种来源信息
- 3702 - Arabidopsis thaliana:
- 9606 - Homo sapiens: -
- 33090 - Plants: -
- 28511 - Pogostemon cablin: 10.1021/JF304466T
- 28901 - Salmonella enterica: 10.1039/C3MB25598K
- 5691 - Trypanosoma brucei: 10.1128/AAC.00044-13
- 13750 - Vaccinium macrocarpon: 10.1021/JF061058L
- 569774 - 金线莲: -
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
- Zhibing Lu, Xiaohua Feng, Ling Song, Ying Han, Alexander Kim, Osnat Herzberg, William R Woodson, Brian M Martin, Patrick S Mariano, Debra Dunaway-Mariano. Diversity of function in the isocitrate lyase enzyme superfamily: the Dianthus caryophyllus petal death protein cleaves alpha-keto and alpha-hydroxycarboxylic acids.
Biochemistry.
2005 Dec; 44(50):16365-76. doi:
10.1021/bi051776l
. [PMID: 16342929]