7-(Benzyloxy)-4-(trifluoromethyl)-2H-chromen-2-one (BioDeep_00000841935)

   


代谢物信息卡片


7-(Benzyloxy)-4-(trifluoromethyl)-2H-chromen-2-one

化学式: C17H11F3O3 (320.0660252)
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)COC2=CC3=C(C=C2)C(=CC(=O)O3)C(F)(F)F
InChI: InChI=1S/C17H11F3O3/c18-17(19,20)14-9-16(21)23-15-8-12(6-7-13(14)15)22-10-11-4-2-1-3-5-11/h1-9H,10H2

描述信息

同义名列表

1 个代谢物同义名

7-(Benzyloxy)-4-(trifluoromethyl)-2H-chromen-2-one



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

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代谢反应

0 个相关的代谢反应过程信息。

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BioCyc(0)

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Plant Reactome(0)

INOH(0)

PlantCyc(0)

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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

  • A Stefanski, M Mevissen, A-M Möller, K Kuehni-Boghenbor, A Schmitz. Induction of cytochrome P450 enzymes in primary equine hepatocyte culture. Toxicology in vitro : an international journal published in association with BIBRA. 2013 Oct; 27(7):2023-30. doi: 10.1016/j.tiv.2013.07.009. [PMID: 23916975]
  • Christiaan J Malherbe, Dalene De Beer, Elizabeth Joubert. Development of on-line high performance liquid chromatography (HPLC)-biochemical detection methods as tools in the identification of bioactives. International journal of molecular sciences. 2012; 13(3):3101-3133. doi: 10.3390/ijms13033101. [PMID: 22489144]
  • Robert D Finn, Lesley A McLaughlin, Sebastien Ronseaux, Ian Rosewell, J Brian Houston, Colin J Henderson, C Roland Wolf. Defining the in Vivo Role for cytochrome b5 in cytochrome P450 function through the conditional hepatic deletion of microsomal cytochrome b5. The Journal of biological chemistry. 2008 Nov; 283(46):31385-93. doi: 10.1074/jbc.m803496200. [PMID: 18805792]
  • Torstein Schrøder Hansen, Odd Georg Nilsen. In vitro CYP3A4 metabolism: inhibition by Echinacea purpurea and choice of substrate for the evaluation of herbal inhibition. Basic & clinical pharmacology & toxicology. 2008 Nov; 103(5):445-9. doi: 10.1111/j.1742-7843.2008.00307.x. [PMID: 18947363]
  • Miao Hao, Yuqing Zhao, Peizhan Chen, He Huang, Hong Liu, Hualiang Jiang, Ruiwen Zhang, Hui Wang. Structure-activity relationship and substrate-dependent phenomena in effects of ginsenosides on activities of drug-metabolizing P450 enzymes. PloS one. 2008 Jul; 3(7):e2697. doi: 10.1371/journal.pone.0002697. [PMID: 18628990]
  • Steven H Yale, Ingrid Glurich. Analysis of the inhibitory potential of Ginkgo biloba, Echinacea purpurea, and Serenoa repens on the metabolic activity of cytochrome P450 3A4, 2D6, and 2C9. Journal of alternative and complementary medicine (New York, N.Y.). 2005 Jun; 11(3):433-9. doi: 10.1089/acm.2005.11.433. [PMID: 15992226]