AI3-26793 (BioDeep_00000868787)

Main id: BioDeep_00000017689

 

PANOMIX_OTCML-2023


代谢物信息卡片


InChI=1\C8H11N\c1-9-7-8-5-3-2-4-6-8\h2-6,9H,7H2,1H

化学式: C8H11N (121.0891446)
中文名称: N-苄基甲胺
谱图信息: 最多检出来源 () 0%

分子结构信息

SMILES: CNCC1=CC=CC=C1
InChI: InChI=1S/C8H11N/c1-9-7-8-5-3-2-4-6-8/h2-6,9H,7H2,1H3

描述信息

N-methylbenzylamine is a member of phenylmethylamines. N-methylbenzylamine can be found in carrot, which makes N-methylbenzylamine a potential biomarker for the consumption of these food products[1].
N-methylbenzylamine is a member of phenylmethylamines. N-methylbenzylamine can be found in carrot, which makes N-methylbenzylamine a potential biomarker for the consumption of these food products[1].

同义名列表

38 个代谢物同义名

InChI=1\C8H11N\c1-9-7-8-5-3-2-4-6-8\h2-6,9H,7H2,1H; N-Methyl aminomethylated polystyrene; N-Methylaminomethyl polystyrene; Benzenemethanamine, N-methyl-; N-methyl-1-phenyl-methanamine; Benzylamine, N-methyl- (8CI); N-methyl-1-phenylmethanamine; 13426-94-3 (HYDROCHLORIDE); N-benzyl-N-methylamine; Benzylamine, N-methyl-; BENZYLAMINE, N-METHYL; N-Methy-N-benzylamine; SDCCGMLS-0066901.P001; N-Methylbenzylamine; Benzyl(methyl)amine; N-Benzylmethylamine; Benzyl-methyl-amine; Benzylmethylamine; Methylbenzylamine; Spectrum5_000347; EINECS 203-133-4; Spectrum4_001764; NCGC00166047-01; Spectrum_001362; 538779_ALDRICH; B25606_ALDRICH; KBioSS_001842; KBioGR_002247; KBio2_006978; KBio2_001842; KBio2_004410; AIDS-011069; AIDS011069; AI3-26793; NSC 8059; 103-67-3; 1AMA-0-0; NSC8059



数据库引用编号

4 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)

2 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

  • Nachwa Jarkas, Ronald J Voll, Larry Williams, Mark M Goodman. Validation of two fluoro-analogues of N,N-dimethyl-2-(2'-amino-4'-hydroxymethyl-phenylthio)benzylamine as serotonin transporter imaging agents using microPET. Nuclear medicine and biology. 2010 Jul; 37(5):593-603. doi: 10.1016/j.nucmedbio.2010.03.004. [PMID: 20610164]
  • A A N de Paula, J B L Martins, M L dos Santos, L de C Nascente, L A S Romeiro, T F M A Areas, K S T Vieira, N F Gambôa, N G Castro, R Gargano. New potential AChE inhibitor candidates. European journal of medicinal chemistry. 2009 Sep; 44(9):3754-9. doi: 10.1016/j.ejmech.2009.03.045. [PMID: 19446931]
  • Takeshi Kumazawa, Chika Hasegawa, Xiao-Pen Lee, Kenji Hara, Hiroshi Seno, Osamu Suzuki, Keizo Sato. Simultaneous determination of methamphetamine and amphetamine in human urine using pipette tip solid-phase extraction and gas chromatography-mass spectrometry. Journal of pharmaceutical and biomedical analysis. 2007 Jun; 44(2):602-7. doi: 10.1016/j.jpba.2006.12.025. [PMID: 17267160]
  • Nicola J Curtin, Hannah C Barlow, Karen J Bowman, A Hilary Calvert, Richard Davison, Bernard T Golding, Bing Huang, Peter J Loughlin, David R Newell, Peter G Smith, Roger J Griffin. Resistance-modifying agents. 11.(1) Pyrimido[5,4-d]pyrimidine modulators of antitumor drug activity. Synthesis and structure-activity relationships for nucleoside transport inhibition and binding to alpha1-acid glycoprotein. Journal of medicinal chemistry. 2004 Sep; 47(20):4905-22. doi: 10.1021/jm040772w. [PMID: 15369395]
  • A Pagliara, B Testa, P A Carrupt, P Jolliet, C Morin, D Morin, S Urien, J P Tillement, J P Rihoux. Molecular properties and pharmacokinetic behavior of cetirizine, a zwitterionic H1-receptor antagonist. Journal of medicinal chemistry. 1998 Mar; 41(6):853-63. doi: 10.1021/jm9704311. [PMID: 9526560]
  • Y Xu, C Han. [Prevention of in vivo formation of NMBz A and the formation of oesophageal tumour by tea in rats]. Zhonghua yu fang yi xue za zhi [Chinese journal of preventive medicine]. 1991 Jul; 25(4):201-4. doi: ". [PMID: 1782821]
  • F Karoum. N-propargylbenzylamine, a major metabolite of pargyline, is a potent inhibitor of monoamine oxidase type B in rats in vivo: a comparison with deprenyl. British journal of pharmacology. 1987 Feb; 90(2):335-45. doi: 10.1111/j.1476-5381.1987.tb08963.x. [PMID: 3103805]
  • L Giuliani, G Carmignani, E Belgrano, P Puppo. Transcatheter arterial embolization in urological tumors: the use of isobutyl-2-cyanoacrylate. The Journal of urology. 1979 May; 121(5):630-4. doi: 10.1016/s0022-5347(17)56913-x. [PMID: 439260]
  • A W Mondorf. [Evidence of urinary tubular proteins in inflammatory and toxic kidney damage]. Wiener medizinische Wochenschrift. Supplement. 1975; 27(?):20-3. doi: NULL. [PMID: 5816]