2-((3-Oxo-3-phenylpropyl)amino)acetic acid (BioDeep_00000840599)
代谢物信息卡片
化学式: C11H13NO3 (207.0895388)
中文名称:
谱图信息:
最多检出来源 () 0%
分子结构信息
SMILES: C1=CC=C(C=C1)C(=O)CCNCC(=O)O
InChI: InChI=1S/C11H13NO3/c13-10(6-7-12-8-11(14)15)9-4-2-1-3-5-9/h1-5,12H,6-8H2,(H,14,15)
相关代谢途径
Reactome(0)
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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)
COVID-19 Disease Map(0)
PathBank(0)
PharmGKB(0)
0 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
- Hae Rim Jung, Yumi Oh, Dongjun Jang, Seungjae Shin, Soo-Jin Lee, Jiwon Kim, Sang Eun Lee, Jaeik Oh, Giyong Jang, Obin Kwon, Yeonmi Lee, Hui-Young Lee, Sung-Yup Cho. Gut bacteria-derived 3-phenylpropionylglycine mitigates adipocyte differentiation of 3T3-L1 cells by inhibiting adiponectin-PPAR pathway.
Genes & genomics.
2023 01; 45(1):71-81. doi:
10.1007/s13258-022-01332-y. [PMID: 36434390] - B Flath, B Rolinski, A A Roscher. Simple high-performance liquid chromatographic method for the detection of phenylpropionylglycine in urine as a diagnostic tool in inherited medium-chain acyl-coenzyme A dehydrogenase deficiency.
Journal of chromatography. B, Biomedical sciences and applications.
1997 Jun; 694(1):227-32. doi:
10.1016/s0378-4347(97)00145-x. [PMID: 9234867] - A Bhala, M J Bennett, K L McGowan, D E Hale. Limitations of 3-phenylpropionylglycine in early screening for medium-chain acyl-coenzyme A dehydrogenase deficiency.
The Journal of pediatrics.
1993 Jan; 122(1):100-3. doi:
10.1016/s0022-3476(05)83499-7. [PMID: 8419594] - J F Glasgow, R Moore, P H Robinson, P J McKiernan. The phenylpropionic acid load test: experience with 72 children at-risk for beta-oxidation disorders.
Irish journal of medical science.
1992 Oct; 161(10):586-8. doi:
10.1007/bf02942363. [PMID: 1478838] - M J Bennett, A Bhala, S F Poirier, M C Ragni, S M Willi, D E Hale. When do gut flora in the newborn produce 3-phenylpropionic acid? Implications for early diagnosis of medium-chain acyl-CoA dehydrogenase deficiency.
Clinical chemistry.
1992 Feb; 38(2):278-81. doi:
. [PMID: 1541011] - M J Bennett, R J Pollitt, L S Taitz, S Variend. Medium-chain acyl-CoA dehydrogenase deficiency: a useful diagnosis five years after death.
Clinical chemistry.
1990 Sep; 36(9):1695-7. doi:
. [PMID: 2208722] - M J Bennett, P M Coates, D E Hale, D S Millington, R J Pollitt, P Rinaldo, C R Roe, K Tanaka. Analysis of abnormal urinary metabolites in the newborn period in medium-chain acyl-CoA dehydrogenase deficiency.
Journal of inherited metabolic disease.
1990; 13(5):707-15. doi:
10.1007/bf01799572. [PMID: 2246856] - P Rinaldo, J J O'Shea, R D Welch, K Tanaka. Stable isotope dilution analysis of n-hexanoylglycine, 3-phenylpropionylglycine and suberylglycine in human urine using chemical ionization gas chromatography/mass spectrometry selected ion monitoring.
Biomedical & environmental mass spectrometry.
1989 Jul; 18(7):471-7. doi:
10.1002/bms.1200180705. [PMID: 2775902] - P Rinaldo, J J O'Shea, P M Coates, D E Hale, C A Stanley, K Tanaka. Medium-chain acyl-CoA dehydrogenase deficiency. Diagnosis by stable-isotope dilution measurement of urinary n-hexanoylglycine and 3-phenylpropionylglycine.
The New England journal of medicine.
1988 Nov; 319(20):1308-13. doi:
10.1056/nejm198811173192003. [PMID: 3054550] - J W Seakins, G Rumsby. The use of phenylpropionic acid as a loading test for medium-chain acyl-CoA dehydrogenase deficiency.
Journal of inherited metabolic disease.
1988; 11 Suppl 2(?):221-4. doi:
10.1007/bf01804241. [PMID: 3141707]