H-Dab.HBr (BioDeep_00000875166)
Main id: BioDeep_00000001361
PANOMIX_OTCML-2023
代谢物信息卡片
化学式: C4H10N2O2 (118.0742)
中文名称: L-2,4-二氨基丁酸氢溴酸盐
谱图信息:
最多检出来源 () 0%
分子结构信息
SMILES: C(CN)C(C(=O)O)N
InChI: InChI=1S/C4H10N2O2/c5-2-1-3(6)4(7)8/h3H,1-2,5-6H2,(H,7,8)/t3-/m0/s1
描述信息
A 2,4-diaminobutyric acid that has S-configuration.
2,4-diaminobutyric acid, also known as L-2,4-diaminobutanoate or alpha,gamma-diaminobutyrate, is a member of the class of compounds known as L-alpha-amino acids. L-alpha-amino acids are alpha amino acids which have the L-configuration of the alpha-carbon atom. 2,4-diaminobutyric acid is soluble (in water) and a moderately acidic compound (based on its pKa). 2,4-diaminobutyric acid can be synthesized from butyric acid. 2,4-diaminobutyric acid is also a parent compound for other transformation products, including but not limited to, N(4)-acetyl-L-2,4-diaminobutyric acid, (2S)-2-acetamido-4-aminobutanoic acid, and L-alpha-amino-gamma-oxalylaminobutyric acid. 2,4-diaminobutyric acid can be found in a number of food items such as caraway, chia, atlantic herring, and chayote, which makes 2,4-diaminobutyric acid a potential biomarker for the consumption of these food products. 2,4-diaminobutyric acid can be found primarily in blood and urine. Moreover, 2,4-diaminobutyric acid is found to be associated with alzheimers disease.
L-DABA (L-2,4-Diaminobutyric acid) is a week GABA transaminase inhibitor with an IC50 of larger than 500 μM; exhibits antitumor activity in vivo and in vitro.
L-DABA (L-2,4-Diaminobutyric acid) is a week GABA transaminase inhibitor with an IC50 of larger than 500 μM; exhibits antitumor activity in vivo and in vitro.
同义名列表
数据库引用编号
15 个数据库交叉引用编号
- ChEBI: CHEBI:48950
- KEGG: C03283
- PubChem: 134490
- DrugBank: DB03817
- ChEMBL: CHEMBL321357
- foodb: FDB030953
- CAS: 1758-80-1
- MetaboLights: MTBLC48950
- PubChem: 6142
- KNApSAcK: C00001353
- PDB-CCD: DAB
- 3DMET: B00574
- NIKKAJI: J80.310C
- medchemexpress: HY-101414
- KNApSAcK: 48950
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)
4 个相关的物种来源信息
- 3039 - Euglena gracilis: 10.3389/FBIOE.2021.662655
- 154494 - Lathyrus latifolius: 10.1016/S0031-9422(96)00425-6
- 1886 - Streptomyces albidoflavus: 10.1128/AEM.01992-09
- 1902 - Streptomyces coelicolor: 10.1128/AEM.01992-09
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
- Sea-Yong Kim, Per Hedberg, Monika Winder, Sara Rydberg. Evidence of 2,4-diaminobutyric acid (DAB) production as a defense mechanism in diatom Thalassiosira pseudonana.
Aquatic toxicology (Amsterdam, Netherlands).
2022 Aug; 249(?):106210. doi:
10.1016/j.aquatox.2022.106210
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Ecotoxicology and environmental safety.
2021 Jan; 208(?):111515. doi:
10.1016/j.ecoenv.2020.111515
. [PMID: 33099142] - Le-Ni Sun, Dan-Dan Pan, Xiang-Wei Wu, En-Dong Yang, Ri-Mao Hua, Qing X Li. Leucobacter triazinivorans sp. nov., a s-triazine herbicide prometryn-degrading bacterium isolated from sludge.
International journal of systematic and evolutionary microbiology.
2018 Jan; 68(1):204-210. doi:
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. [PMID: 29139349] - Peter B Nunn, Geoffrey A Codd. Metabolic solutions to the biosynthesis of some diaminomonocarboxylic acids in nature: Formation in cyanobacteria of the neurotoxins 3-N-methyl-2,3-diaminopropanoic acid (BMAA) and 2,4-diaminobutanoic acid (2,4-DAB).
Phytochemistry.
2017 Dec; 144(?):253-270. doi:
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2017 Jul; 67(7):2248-2252. doi:
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Analytical and bioanalytical chemistry.
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Toxins.
2014 Jan; 6(2):488-508. doi:
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Biochimica et biophysica acta.
2012 Jul; 1818(7):1663-72. doi:
10.1016/j.bbamem.2012.03.001
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Current microbiology.
2012 May; 64(5):441-8. doi:
10.1007/s00284-012-0089-4
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International journal of systematic and evolutionary microbiology.
2012 Apr; 62(Pt 4):786-790. doi:
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Journal of microbiology (Seoul, Korea).
2012 Feb; 50(1):161-5. doi:
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International journal of systematic and evolutionary microbiology.
2011 Mar; 61(Pt 3):502-506. doi:
10.1099/ijs.0.021360-0
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Toxins.
2011 03; 3(3):260-93. doi:
10.3390/toxins3030260
. [PMID: 22069709] - E Martin, N Lodders, U Jäckel, P Schumann, P Kämpfer. Leucobacter aerolatus sp. nov., from the air of a duck barn.
International journal of systematic and evolutionary microbiology.
2010 Dec; 60(Pt 12):2838-2842. doi:
10.1099/ijs.0.021303-0
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International journal of systematic and evolutionary microbiology.
2010 Apr; 60(Pt 4):866-870. doi:
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. [PMID: 19661491] - Thomas Krüger, Bettina Mönch, Steven Oppenhäuser, Bernd Luckas. LC-MS/MS determination of the isomeric neurotoxins BMAA (beta-N-methylamino-L-alanine) and DAB (2,4-diaminobutyric acid) in cyanobacteria and seeds of Cycas revoluta and Lathyrus latifolius.
Toxicon : official journal of the International Society on Toxinology.
2010 Feb; 55(2-3):547-57. doi:
10.1016/j.toxicon.2009.10.009
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International journal of systematic and evolutionary microbiology.
2008 Nov; 58(Pt 11):2574-8. doi:
10.1099/ijs.0.2008/001065-0
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2007 Feb; 57(Pt 2):405-408. doi:
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Journal of neurobiology.
2004 Nov; 61(2):189-208. doi:
10.1002/neu.20061
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Cancer gene therapy.
2004 Feb; 11(2):103-8. doi:
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Journal of molecular biology.
2002 Jan; 315(2):103-11. doi:
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British journal of pharmacology.
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2001 Nov; 51(Pt 6):2073-2079. doi:
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Cancer chemotherapy and pharmacology.
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Nature.
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