Nonox D (BioDeep_00000859762)

   


代谢物信息卡片


InChI=1\C16H13N\c1-2-8-15(9-3-1)17-16-11-10-13-6-4-5-7-14(13)12-16\h1-12,17

化学式: C16H13N (219.1047938)
中文名称: N-苯基-2-萘胺
谱图信息: 最多检出来源 () 0%

分子结构信息

SMILES: C1=CC=C(C=C1)NC2=CC3=CC=CC=C3C=C2
InChI: InChI=1S/C16H13N/c1-2-8-15(9-3-1)17-16-11-10-13-6-4-5-7-14(13)12-16/h1-12,17H

描述信息

同义名列表

64 个代谢物同义名

InChI=1\C16H13N\c1-2-8-15(9-3-1)17-16-11-10-13-6-4-5-7-14(13)12-16\h1-12,17; 4-12-00-03128 (Beilstein Handbook Reference); N-Phenyl-.beta.-amino-naphthalene; N-Fenyl-2-aminonaftalen [Czech]; Fenyl-beta-naftylamin [Czech]; N-Phenyl-.beta.-naphthylamine; 2-Naphthalenamine, N-phenyl-; N-Phenyl-beta-naphthylamine; Phenyl-.beta.-naphthylamine; 2-Naphthylamine, N-phenyl-; .beta.-Naphthylphenylamine; N-Phenyl-2-naphthalenamine; N-Phenylnaphthalen-2-amine; Phenyl-beta-naphthylamine; 2-Phenylaminonaphthalene; Phenyl-beta-naphtilamine; N-Phenyl-2-naphthylamine; beta-Naphthylphenylamine; 2-naphthyl-phenyl-amine; Phenyl-2-naphthylamine; 2-Naphthylphenylamine; N-(2-Naphthyl)aniline; 2-Anilinonaphthalene; N-2-Naphthylaniline; Anilinonaphthalene; AK 1 (stabilizer); EINECS 205-223-9; Antioxidant 116; NCGC00091111-02; Antioxidant PBN; Stabilizator ar; NCGC00091111-01; Agerite powder; 178055_ALDRICH; WLN: L66J CMR; Oprea1_737712; Stabilizer ar; ZINC01669780; Vulkanox PBN; BRN 2211188; AIDS-417346; 84420-28-0; AIDS417346; NCI-C02915; Noclizer D; Nilox pbna; 52907-17-2; AI3-00068; ST5165453; HSDB 2888; aceto PBN; NSC 37151; CCRIS 853; Neozone D; Nonox DN; Nocrac D; 135-88-6; NSC37151; Neozon D; Naftam 2; Nonox D; Neozone; C14694; AK 1



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)

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

  • Long Cheng, Yan He, Yun Tian, Biyun Liu, Yongyuan Zhang, Qiaohong Zhou, Zhenbin Wu. Comparative biotoxicity of N-Phenyl-1-naphthylamine and N-Phenyl-2-naphthylamine on cyanobacteria Microcystis aeruginosa. Chemosphere. 2017 Jun; 176(?):183-191. doi: 10.1016/j.chemosphere.2017.02.110. [PMID: 28260658]
  • L A Lomovatskaya, L E Makarova, O V Kuzakova, A S Romanenko, A M Goncharova. [Effect of N-phenyl-2-naphthylamine on activity of adenylate cyclase signal system components and virulence of bacterial phytopathogens and mutualists]. Prikladnaia biokhimiia i mikrobiologiia. 2016 May; 52(3):306-11. doi: . [PMID: 29509386]
  • Tobias Weiss, Hermann M Bolt, Gerhard Schlüter, Stephan Koslitz, Dirk Taeger, Peter Welge, Thomas Brüning. Metabolic dephenylation of the rubber antioxidant N-phenyl-2-naphthylamine to carcinogenic 2-naphthylamine in rats. Archives of toxicology. 2013 Jul; 87(7):1265-72. doi: 10.1007/s00204-013-1025-5. [PMID: 23423714]
  • L E Makarova, V I Smirnov, L V Klyba, I G Petrova, L V Dudareva. [Role of allelopathic compositions in the regulation and development of legume-rhizobial symbiosis]. Prikladnaia biokhimiia i mikrobiologiia. 2012 Jul; 48(4):394-402. doi: ". [PMID: 23035572]
  • Haifeng Qian, Xiaoyan Xu, Wei Chen, Hong Jiang, Yuanxiang Jin, Weiping Liu, Zhengwei Fu. Allelochemical stress causes oxidative damage and inhibition of photosynthesis in Chlorella vulgaris. Chemosphere. 2009 Apr; 75(3):368-75. doi: 10.1016/j.chemosphere.2008.12.040. [PMID: 19171365]
  • Tobias Weiss, Thomas Brüning, Hermann M Bolt. Dephenylation of the rubber chemical N-phenyl-2-naphthylamine to carcinogenic 2-naphthylamine: a classical problem revisited. Critical reviews in toxicology. 2007; 37(7):553-66. doi: 10.1080/10408440701419637. [PMID: 17674211]
  • Rolf Altenburger, Werner Brack, William R Greco, Matthias Grote, Klaus Jung, Agnes Ovari, Janet Riedl, Katrin Schwab, Eberhard Küster. On the mode of action of N-phenyl-2-naphthylamine in plants. Environmental science & technology. 2006 Oct; 40(19):6163-9. doi: 10.1021/es060338e. [PMID: 17051816]
  • G Carlucci, L Airoldi, R Fanelli, B Laguzzi. Quantitative analysis of aromatic amines in human urine by gas chromatography-mass spectrometry-selected-ion monitoring. Journal of chromatography. 1984 Nov; 311(1):141-7. doi: 10.1016/s0378-4347(00)84700-3. [PMID: 6520155]
  • S Laham, M Potvin. Biological conversion of N-phenyl-2-naphthylamine to 2-naphthylamine in the Sprague-Dawley rat. Drug and chemical toxicology. 1983; 6(3):295-309. doi: 10.3109/01480548309017820. [PMID: 6628262]
  • P L Batten, D E Hathway. Dephenylation of N-phenyl-2-naphthylamine in dogs and its possible oncogenic implications. British journal of cancer. 1977 Mar; 35(3):342-6. doi: 10.1038/bjc.1977.48. [PMID: 856239]