S-Trichlorovinyl-N-acetylcysteine (BioDeep_00000846637)

   


代谢物信息卡片


S-Trichlorovinyl-N-acetylcysteine

化学式: C7H8Cl3NO3S (290.92904680000004)
中文名称:
谱图信息: 最多检出来源 () 0%

分子结构信息

SMILES: CC(=O)NC(CSC(=C(Cl)Cl)Cl)C(=O)O
InChI: InChI=1S/C7H8Cl3NO3S/c1-3(12)11-4(7(13)14)2-15-6(10)5(8)9/h4H,2H2,1H3,(H,11,12)(H,13,14)/t4-/m0/s1

描述信息

同义名列表

1 个代谢物同义名

S-Trichlorovinyl-N-acetylcysteine



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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INOH(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

  • Tammie R Covington, P Robinan Gentry, Cynthia B Van Landingham, Melvin E Andersen, Janet E Kester, Harvey J Clewell. The use of Markov chain Monte Carlo uncertainty analysis to support a Public Health Goal for perchloroethylene. Regulatory toxicology and pharmacology : RTP. 2007 Feb; 47(1):1-18. doi: 10.1016/j.yrtph.2006.06.008. [PMID: 16901594]
  • W Völkel, A Pähler, W Dekant. Gas chromatography-negative ion chemical ionization mass spectrometry as a powerful tool for the detection of mercapturic acids and DNA and protein adducts as biomarkers of exposure to halogenated olefins. Journal of chromatography. A. 1999 Jun; 847(1-2):35-46. doi: 10.1016/s0021-9673(99)00022-9. [PMID: 10431350]
  • W Völkel, M Friedewald, E Lederer, A Pähler, J Parker, W Dekant. Biotransformation of perchloroethene: dose-dependent excretion of trichloroacetic acid, dichloroacetic acid, and N-acetyl-S-(trichlorovinyl)-L-cysteine in rats and humans after inhalation. Toxicology and applied pharmacology. 1998 Nov; 153(1):20-7. doi: 10.1006/taap.1998.8548. [PMID: 9875296]
  • G Birner, A Rutkowska, W Dekant. N-acetyl-S-(1,2,2-trichlorovinyl)-L-cysteine and 2,2,2-trichloroethanol: two novel metabolites of tetrachloroethene in humans after occupational exposure. Drug metabolism and disposition: the biological fate of chemicals. 1996 Jan; 24(1):41-8. doi: . [PMID: 8825189]
  • M J Bartels. Quantitation of the tetrachloroethylene metabolite N-acetyl-S-(trichlorovinyl)cysteine in rat urine via negative ion chemical ionization gas chromatography/tandem mass spectrometry. Biological mass spectrometry. 1994 Nov; 23(11):689-94. doi: 10.1002/bms.1200231107. [PMID: 7811758]
  • S Vamvakas, W Dekant, K Berthold, S Schmidt, D Wild, D Henschler. Enzymatic transformation of mercapturic acids derived from halogenated alkenes to reactive and mutagenic intermediates. Biochemical pharmacology. 1987 Sep; 36(17):2741-8. doi: 10.1016/0006-2952(87)90258-9. [PMID: 3307787]
  • W Dekant, M Metzler, D Henschler. Identification of S-1,2,2-trichlorovinyl-N-acetylcysteine as a urinary metabolite of tetrachloroethylene: bioactivation through glutathione conjugation as a possible explanation of its nephrocarcinogenicity. Journal of biochemical toxicology. 1986 Jun; 1(2):57-72. doi: 10.1002/jbt.2570010206. [PMID: 3271876]
  • 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]