BENZANILIDE (BioDeep_00000275440)

   


代谢物信息卡片


BENZANILIDE

化学式: C13H11NO (197.0841)
中文名称: N-苯甲酰替苯胺
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)NC2=CC=CC=C2
InChI: InChI=1S/C13H11NO/c15-13(11-7-3-1-4-8-11)14-12-9-5-2-6-10-12/h1-10H,(H,14,15)

描述信息

CONFIDENCE standard compound; INTERNAL_ID 8081

同义名列表

1 个代谢物同义名

BENZANILIDE



数据库引用编号

5 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)

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

  • Trent Kunkle, Sanofar Abdeen, Nilshad Salim, Anne-Marie Ray, Mckayla Stevens, Andrew J Ambrose, José Victorino, Yangshin Park, Quyen Q Hoang, Eli Chapman, Steven M Johnson. Hydroxybiphenylamide GroEL/ES Inhibitors Are Potent Antibacterials against Planktonic and Biofilm Forms of Staphylococcus aureus. Journal of medicinal chemistry. 2018 12; 61(23):10651-10664. doi: 10.1021/acs.jmedchem.8b01293. [PMID: 30392371]
  • Sarah R Dennison, Timothy J Snape, David A Phoenix. Thermodynamic interactions of a cis and trans benzanilide with Escherichia coli bacterial membranes. European biophysics journal : EBJ. 2012 Aug; 41(8):687-93. doi: 10.1007/s00249-012-0835-3. [PMID: 22782185]
  • Joanne V Allen, Catherine Bardelle, Kevin Blades, Dave Buttar, Louise Chapman, Nicola Colclough, Alexander G Dossetter, Andrew P Garner, Alan Girdwood, Christine Lambert, Andrew G Leach, Brian Law, John Major, Helen Plant, Anthony M Slater. The discovery of benzanilides as c-Met receptor tyrosine kinase inhibitors by a directed screening approach. Bioorganic & medicinal chemistry letters. 2011 Sep; 21(18):5224-9. doi: 10.1016/j.bmcl.2011.07.047. [PMID: 21835616]
  • Andrew K L Goey, Rolf W Sparidans, Irma Meijerman, Hilde Rosing, Jan H M Schellens, Jos H Beijnen. A sensitive LC-MS/MS method for the quantitative analysis of the Echinacea purpurea constituent undeca-2-ene-8,10-diynoic acid isobutylamide in human plasma. Journal of chromatography. B, Analytical technologies in the biomedical and life sciences. 2011 Jan; 879(1):41-8. doi: 10.1016/j.jchromb.2010.11.007. [PMID: 21123121]
  • Karin Woelkart, Reginald F Frye, Hartmut Derendorf, Rudolf Bauer, Veronika Butterweck. Pharmacokinetics and tissue distribution of dodeca-2E,4E,8E,10E/Z-tetraenoic acid isobutylamides after oral administration in rats. Planta medica. 2009 Oct; 75(12):1306-13. doi: 10.1055/s-0029-1185631. [PMID: 19399718]
  • Matthew Danish, Erin R Gardner, Xiaohong Chen, William D Figg. Determination of a benzamide histone deacetylase inhibitor, MS-275, in human plasma by liquid chromatography with mass-spectrometric detection. Journal of chromatography. B, Analytical technologies in the biomedical and life sciences. 2009 Jan; 877(3):355-9. doi: 10.1016/j.jchromb.2008.12.018. [PMID: 19117815]
  • Yoshiaki Shimada, Nobuaki Taniguchi, Akira Matsuhisa, Takeyuki Yatsu, Atsuo Tahara, Akihiro Tanaka. Preparation of non-peptide, highly potent and selective antagonists of arginine vasopressin V1A receptor by introduction of alkoxy groups. Chemical & pharmaceutical bulletin. 2003 Sep; 51(9):1075-80. doi: 10.1248/cpb.51.1075. [PMID: 12951451]
  • B Dietz, J Heilmann, R Bauer. Absorption of dodeca-2E,4E,8Z,10E/Z-tetraenoic acid isobutylamides after oral application of Echinacea purpurea tincture. Planta medica. 2001 Dec; 67(9):863-4. doi: 10.1055/s-2001-18846. [PMID: 11745026]
  • S C Mitchell, H M Norbury, R H Waring, P M Gadsden, P B Wood. A comparison of the metabolism and elimination of benzanilide and salicylanilide in the rat. Xenobiotica; the fate of foreign compounds in biological systems. 1982 Feb; 12(2):93-9. doi: 10.3109/00498258209046782. [PMID: 7090426]