N-Methylalanine (BioDeep_00000003148)
Secondary id: BioDeep_00000181323, BioDeep_00000400253, BioDeep_00001868905
natural product human metabolite PANOMIX_OTCML-2023
代谢物信息卡片
化学式: C4H9NO2 (103.0633)
中文名称: N-甲基-DL-丙氨酸, NG-甲基-L-精氨酸, N-甲基丙氨酸, N-甲基-L-丙氨酸
谱图信息:
最多检出来源 Homo sapiens(blood) 20.48%
分子结构信息
SMILES: CC(C(=O)O)NC
InChI: InChI=1S/C4H9NO2/c1-3(5-2)4(6)7/h3,5H,1-2H3,(H,6,7)
描述信息
N-Methylalanine, also known as (S)-2-methylaminopropanoate or N-methyl-L-alanine, is classified as an alanine or an alanine derivative. Alanines are compounds containing alanine or a derivative thereof resulting from reaction of alanine at the amino group or the carboxy group, or from the replacement of any hydrogen of glycine by a heteroatom. N-Methylalanine is considered to be soluble (in water) and acidic. (ChemoSummarizer)
Acquisition and generation of the data is financially supported in part by CREST/JST.
KEIO_ID M028
同义名列表
14 个代谢物同义名
N-Methylalanine hydrochloride, (DL-ala)-isomer; N-Methylalanine hydrobromide, (L-ala)-isomer; (2S)-2-(methylamino)propanoic acid; N-Methylalanine, (beta-ala)-isomer; N-Methylalanine, (L-ala)-isomer; (S)-2-Methylaminopropanoic acid; (S)-2-Methylaminopropanoate; N-Methyl-DL-alanine; N-Me-DL-Ala-OH.HCl; N-Methyl-L-alanine; N-Methylalanine; N-Methylalanine; N-Methyl-L-alanine; N-Methyl-L-alanine
数据库引用编号
29 个数据库交叉引用编号
- ChEBI: CHEBI:143269
- ChEBI: CHEBI:17519
- KEGG: C02721
- PubChem: 5288725
- PubChem: 4377
- HMDB: HMDB0094692
- Metlin: METLIN65818
- ChEMBL: CHEMBL1234201
- MetaCyc: CPD-298
- CAS: 28413-45-8
- CAS: 3913-67-5
- CAS: 600-21-5
- MoNA: KO003361
- MoNA: KO001367
- MoNA: KO001366
- MoNA: PS031002
- MoNA: KO001368
- MoNA: KO003359
- MoNA: KO003357
- MoNA: KO003358
- MoNA: PR100184
- MoNA: PS031001
- MoNA: KO003360
- PMhub: MS000008279
- PubChem: 5683
- PDB-CCD: MAA
- NIKKAJI: J130.628F
- RefMet: N-Methylalanine
- KNApSAcK: 17519
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)
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。
文献列表
- Dorottya Nagy-Szakal, Dinesh K Barupal, Bohyun Lee, Xiaoyu Che, Brent L Williams, Ellie J R Kahn, Joy E Ukaigwe, Lucinda Bateman, Nancy G Klimas, Anthony L Komaroff, Susan Levine, Jose G Montoya, Daniel L Peterson, Bruce Levin, Mady Hornig, Oliver Fiehn, W Ian Lipkin. Insights into myalgic encephalomyelitis/chronic fatigue syndrome phenotypes through comprehensive metabolomics.
Scientific reports.
2018 07; 8(1):10056. doi:
10.1038/s41598-018-28477-9. [PMID: 29968805] - Caixia Ren, Jia Liu, Juntuo Zhou, Hui Liang, Yayun Wang, Yinping Sun, Bin Ma, Yuxin Yin. Low levels of serum serotonin and amino acids identified in migraine patients.
Biochemical and biophysical research communications.
2018 02; 496(2):267-273. doi:
10.1016/j.bbrc.2017.11.203. [PMID: 29294327] - Oliver Fiehn, W Timothy Garvey, John W Newman, Kerry H Lok, Charles L Hoppel, Sean H Adams. Plasma metabolomic profiles reflective of glucose homeostasis in non-diabetic and type 2 diabetic obese African-American women.
PloS one.
2010 Dec; 5(12):e15234. doi:
10.1371/journal.pone.0015234. [PMID: 21170321] - Beatrice Adams, Peter Pörzgen, Emily Pittman, Wesley Y Yoshida, Hans E Westenburg, F David Horgen. Isolation and structure determination of malevamide E, a dolastatin 14 analogue, from the marine cyanobacterium Symploca laete-viridis.
Journal of natural products.
2008 May; 71(5):750-4. doi:
10.1021/np070346o. [PMID: 18361518] - Y Nishina, R Miura, H Tojo, Y Miyake, H Watari, K Shiga. A resonance Raman study on the structures of complexes of flavoprotein D-amino acid oxidase.
Journal of biochemistry.
1986 Feb; 99(2):329-37. doi:
10.1093/oxfordjournals.jbchem.a135487. [PMID: 2871015]
