2-Anisidine (BioDeep_00001868031)

Main id: BioDeep_00000012676

 

Volatile Flavor Compounds


代谢物信息卡片


2-Anisidine

化学式: C7H9NO (123.0684104)
中文名称: 邻氨基苯甲醚, 邻茴香胺
谱图信息: 最多检出来源 () 0%

分子结构信息

SMILES: COC1=CC=CC=C1N
InChI: InChI=1S/C7H9NO/c1-9-7-5-3-2-4-6(7)8/h2-5H,8H2,1H3

描述信息

同义名列表

4 个代谢物同义名

2-Anisidine; O-ANISIDINE; ortho-Anisidine; O-Anisidine



数据库引用编号

8 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。



文献列表

  • Rui Gao, Xiangbo Ma, Lihong Liu, Shan Gao, Xianfa Zhang, Yingming Xu, Xiaoli Cheng, Hui Zhao, Lihua Huo. In-situ deposition of POMA/ZnO nanorods array film by vapor phase polymerization for detection of trace ammonia in human exhaled breath at room temperature. Analytica chimica acta. 2022 Mar; 1199(?):339563. doi: 10.1016/j.aca.2022.339563. [PMID: 35227376]
  • D Sangamithirai, S Munusamy, V Narayanan, A Stephen. A strategy to promote the electroactive platform adopting poly(o-anisidine)-silver nanocomposites probed for the voltammetric detection of NADH and dopamine. Materials science & engineering. C, Materials for biological applications. 2017 Nov; 80(?):425-437. doi: 10.1016/j.msec.2017.06.014. [PMID: 28866184]
  • Hiroshi Matsumoto, Fumiyo Saito, Masahiro Takeyoshi. Investigation of the early-response genes in chemical-induced renal carcinogenicity for the prediction of chemical carcinogenicity in rats. The Journal of toxicological sciences. 2017; 42(2):175-181. doi: 10.2131/jts.42.175. [PMID: 28321044]
  • Karel Naiman, Martin Dracínský, Petr Hodek, Markéta Martínková, Heinz H Schmeiser, Eva Frei, Marie Stiborová. Formation, persistence, and identification of DNA adducts formed by the carcinogenic environmental pollutant o-anisidine in rats. Toxicological sciences : an official journal of the Society of Toxicology. 2012 Jun; 127(2):348-59. doi: 10.1093/toxsci/kfs104. [PMID: 22403159]
  • Birgitta Kütting, Thomas Göen, Ursula Schwegler, Hermann Fromme, Wolfgang Uter, Jürgen Angerer, Hans Drexler. Monoarylamines in the general population--a cross-sectional population-based study including 1004 Bavarian subjects. International journal of hygiene and environmental health. 2009 May; 212(3):298-309. doi: 10.1016/j.ijheh.2008.07.004. [PMID: 18789761]
  • Shilpa Ramani, Jayabaskaran Chelliah. UV-B-induced signaling events leading to enhanced-production of catharanthine in Catharanthus roseus cell suspension cultures. BMC plant biology. 2007 Nov; 7(?):61. doi: 10.1186/1471-2229-7-61. [PMID: 17988378]
  • Marie Stiborová, Markéta Miksanová, Miroslav Sulc, Helena Rýdlová, Heinz H Schmeiser, Eva Frei. Identification of a genotoxic mechanism for the carcinogenicity of the environmental pollutant and suspected human carcinogen o-anisidine. International journal of cancer. 2005 Sep; 116(5):667-78. doi: 10.1002/ijc.21122. [PMID: 15828049]
  • Marie Stiborová, Markéta Miksanová, Stanislav Smrcek, Christian A Bieler, Andrea Breuer, Karl A Klokow, Heinz H Schmeiser, Eva Frei. Identification of a genotoxic mechanism for 2-nitroanisole carcinogenicity and of its carcinogenic potential for humans. Carcinogenesis. 2004 May; 25(5):833-40. doi: 10.1093/carcin/bgh061. [PMID: 14729594]
  • Andrzej Sapota, Bogdan Czerski, Marian Jedrzejczak. Tissue distribution, excretion and metabolism of o-anisidine in rats. International journal of occupational medicine and environmental health. 2003; 16(4):351-7. doi: NULL. [PMID: 14964645]
  • Tobias Weiss, Jürgen Angerer. Simultaneous determination of various aromatic amines and metabolites of aromatic nitro compounds in urine for low level exposure using gas chromatography-mass spectrometry. Journal of chromatography. B, Analytical technologies in the biomedical and life sciences. 2002 Oct; 778(1-2):179-92. doi: 10.1016/s0378-4347(01)00542-4. [PMID: 12376125]
  • E Richter, S Rösler, G Scherer, J G Gostomzyk, A Grübl, U Krämer, H Behrendt. Haemoglobin adducts from aromatic amines in children in relation to area of residence and exposure to environmental tobacco smoke. International archives of occupational and environmental health. 2001 Aug; 74(6):421-8. doi: 10.1007/s004200100243. [PMID: 11563605]
  • Y F Sasaki, E Nishidate, Y Q Su, N Matsusaka, S Tsuda, N Susa, Y Furukawa, S Ueno. Organ-specific genotoxicity of the potent rodent bladder carcinogens o-anisidine and p-cresidine. Mutation research. 1998 Jan; 412(2):155-60. doi: 10.1016/s1383-5718(97)00183-6. [PMID: 9539969]