3-(3-Hydroxyphenyl)propanoate (BioDeep_00000897718)

   


代谢物信息卡片


3-(3-Hydroxyphenyl)propanoate

化学式: C9H9O3- (165.0552)
中文名称:
谱图信息: 最多检出来源 () 0%

分子结构信息

SMILES: C1=CC(=CC(=C1)O)CCC(=O)[O-]
InChI: InChI=1S/C9H10O3/c10-8-3-1-2-7(6-8)4-5-9(11)12/h1-3,6,10H,4-5H2,(H,11,12)/p-1

描述信息

A monocarboxylic acid anion that is the conjugate base of 3-(3-hydroxyphenyl)propanoic acid.

同义名列表

1 个代谢物同义名

3-(3-Hydroxyphenyl)propanoate



数据库引用编号

3 个数据库交叉引用编号

分类词条

相关代谢途径

Reactome(0)

BioCyc(1)

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)

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。

亚细胞结构定位 关联基因列表


文献列表

  • Ying Xu, Ning-Yi Zhou. MhpA Is a Hydroxylase Catalyzing the Initial Reaction of 3-(3-Hydroxyphenyl)Propionate Catabolism in Escherichia coli K-12. Applied and environmental microbiology. 2020 02; 86(4):. doi: 10.1128/aem.02385-19. [PMID: 31811039]
  • Noriko Hiraishi, Daisaku Kaneko, Shu Taira, Siqian Wang, Masayuki Otsuki, Junji Tagami. Mussel-mimetic, bioadhesive polymers from plant-derived materials. Journal of investigative and clinical dentistry. 2015 Feb; 6(1):59-62. doi: 10.1111/jicd.12054. [PMID: 23857900]
  • E G Stanley, N J C Bailey, M E Bollard, J N Haselden, C J Waterfield, E Holmes, J K Nicholson. Sexual dimorphism in urinary metabolite profiles of Han Wistar rats revealed by nuclear-magnetic-resonance-based metabonomics. Analytical biochemistry. 2005 Aug; 343(2):195-202. doi: 10.1016/j.ab.2005.01.024. [PMID: 15993369]
  • Laurent Y Rios, Marie-Paule Gonthier, Christian Rémésy, Isabelle Mila, Catherine Lapierre, Sheryl A Lazarus, Gary Williamson, Augustin Scalbert. Chocolate intake increases urinary excretion of polyphenol-derived phenolic acids in healthy human subjects. The American journal of clinical nutrition. 2003 Apr; 77(4):912-8. doi: 10.1093/ajcn/77.4.912. [PMID: 12663291]
  • R E Williams, H W Eyton-Jones, M J Farnworth, R Gallagher, W M Provan. Effect of intestinal microflora on the urinary metabolic profile of rats: a (1)H-nuclear magnetic resonance spectroscopy study. Xenobiotica; the fate of foreign compounds in biological systems. 2002 Sep; 32(9):783-94. doi: 10.1080/00498250210143047. [PMID: 12396275]
  • C L Gavaghan, J K Nicholson, S C Connor, I D Wilson, B Wright, E Holmes. Directly coupled high-performance liquid chromatography and nuclear magnetic resonance spectroscopic with chemometric studies on metabolic variation in Sprague--Dawley rats. Analytical biochemistry. 2001 Apr; 291(2):245-52. doi: 10.1006/abio.2000.5034. [PMID: 11401298]
  • U Justesen, E Arrigoni. Electrospray ionisation mass spectrometric study of degradation products of quercetin, quercetin-3-glucoside and quercetin-3-rhamnoglucoside, produced by in vitro fermentation with human faecal flora. Rapid communications in mass spectrometry : RCM. 2001; 15(7):477-83. doi: 10.1002/rcm.250. [PMID: 11268131]
  • B L Goodwin, C R Ruthven, M Sandler. Gut flora and the origin of some urinary aromatic phenolic compounds. Biochemical pharmacology. 1994 Jun; 47(12):2294-7. doi: 10.1016/0006-2952(94)90268-2. [PMID: 8031324]
  • L A GRIFFITHS. m-Hydroxyphenylpropionic acid, a major urinary metabolite of catechin in the rat. Nature. 1962 Jun; 194(?):869-70. doi: 10.1038/194869b0. [PMID: 13901876]