2-Propenoic acid, 3-(3,4-dimethoxyphenyl)- (BioDeep_00001884129)

   


代谢物信息卡片


2-Propenoic acid, 3-(3,4-dimethoxyphenyl)-

化学式: C11H12O4 (208.0736)
中文名称:
谱图信息: 最多检出来源 () 0%

分子结构信息

SMILES: COC1=C(C=C(C=C1)C=CC(=O)O)OC
InChI: InChI=1S/C11H12O4/c1-14-9-5-3-8(4-6-11(12)13)7-10(9)15-2/h3-7H,1-2H3,(H,12,13)

描述信息

同义名列表

1 个代谢物同义名

2-Propenoic acid, 3-(3,4-dimethoxyphenyl)-



数据库引用编号

2 个数据库交叉引用编号

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)

11 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

  • Tracy L Farrell, Miren Gomez-Juaristi, Laure Poquet, Karine Redeuil, Kornél Nagy, Mathieu Renouf, Gary Williamson. Absorption of dimethoxycinnamic acid derivatives in vitro and pharmacokinetic profile in human plasma following coffee consumption. Molecular nutrition & food research. 2012 Sep; 56(9):1413-23. doi: 10.1002/mnfr.201200021. [PMID: 22865606]
  • Kornél Nagy, Karine Redeuil, Gary Williamson, Serge Rezzi, Fabiola Dionisi, Karin Longet, Frédéric Destaillats, Mathieu Renouf. First identification of dimethoxycinnamic acids in human plasma after coffee intake by liquid chromatography-mass spectrometry. Journal of chromatography. A. 2011 Jan; 1218(3):491-7. doi: 10.1016/j.chroma.2010.11.076. [PMID: 21167490]
  • Dimitra Hadjipavlou-Litina, George E Magoulas, Stavros E Bariamis, Denis Drainas, Konstantinos Avgoustakis, Dionissios Papaioannou. Does conjugation of antioxidants improve their antioxidative/anti-inflammatory potential?. Bioorganic & medicinal chemistry. 2010 Dec; 18(23):8204-17. doi: 10.1016/j.bmc.2010.10.012. [PMID: 21041094]
  • Maher M El-Domiaty, Michael Wink, Mahmoud M Abdel Aal, Maged M Abou-Hashem, Rehab H Abd-Alla. Antihepatotoxic activity and chemical constituents of Buddleja asiatica Lour. Zeitschrift fur Naturforschung. C, Journal of biosciences. 2009 Jan; 64(1-2):11-9. doi: 10.1515/znc-2009-1-203. [PMID: 19323260]
  • Ying Ling Lai, Masayoshi Yamaguchi. Phytocomponent p-hydroxycinnamic acid stimulates bone formation and inhibits bone resorption in rat femoral tissues in vitro. Molecular and cellular biochemistry. 2006 Nov; 292(1-2):45-52. doi: 10.1007/s11010-006-9175-x. [PMID: 17036165]
  • Alexis Zamble, Sevser Sahpaz, Thierry Hennebelle, Pascal Carato, François Bailleul. N1,N5,N10-Tris(4-hydroxycinnamoyl)spermidines from Microdesmis keayana roots. Chemistry & biodiversity. 2006 Sep; 3(9):982-9. doi: 10.1002/cbdv.200690107. [PMID: 17193330]
  • Christian Lindermayr, Judith Fliegmann, Jürgen Ebel. Deletion of a single amino acid residue from different 4-coumarate:CoA ligases from soybean results in the generation of new substrate specificities. The Journal of biological chemistry. 2003 Jan; 278(5):2781-6. doi: 10.1074/jbc.m202632200. [PMID: 12421821]