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Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)
 
Chemical Compound Review: 

PubChem2545     3,4,5,6-tetrachlorobenzene- 1,2-diol

Synonyms: CCRIS 4061, AG-D-43027, ACMC-20fatz, CHEBI:26889, NSC-29027, ...
 
 
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Disease relevance of NSC 29027

 

High impact information on NSC 29027

  • The analogous SERR difference spectroscopy experiment is also carried out for the enzyme-inhibitor (EI) complex of CCD with tetrachlorocatechol (TCC) [2].
  • In contrast, 4c, which is prepared from a 1:2 molar mixture of B(OH)(3) and tetrachlorocatechol, is effective as a Lewis acid-assisted Brønsted acid (LBA) catalyst for Ritter reaction [3].
  • The catechol 1,2-dioxygenase from strain CH34 is unique in its property to transform tetrachlorocatechol; however, excess substrate led to a marked reversible inhibition [4].
  • Product identification suggested that the reaction may include two parallel reactions to form either dimers or 2,3,5,6-tetrachloro-1,4-hydroquinone and tetrachlorocatechol via simultaneous dehydrochlorination and hydroxylation [5].
  • The formation of tetrachlorocatechol during biotransformation was monitored, and its inhibitory effect on growth of strain PH-05 was analyzed at a range of concentrations [6].
 

Biological context of NSC 29027

  • The kinetics of decomposition of tetrachlorobenzo-1,2-quinone in aqueous solutions were studied in detail and showed the formation of tetrachlorocatechol, 2,5-dichloro-3,6-dihydroxybenzo-1,4-quinone, 1,2,3-trihydroxy-4,5,6-trichlorobenzene, 1,2,4-trihydroxy-3,5,6-trichlorobenzene, dichloromaleic acid, and a trichlorocyclopentendione [7].
 

Analytical, diagnostic and therapeutic context of NSC 29027

References

  1. Chlorocatechols substituted at positions 4 and 5 are substrates of the broad-spectrum chlorocatechol 1,2-dioxygenase of Pseudomonas chlororaphis RW71. Potrawfke, T., Armengaud, J., Wittich, R.M. J. Bacteriol. (2001) [Pubmed]
  2. Evidence for retention of biological activity of a non-heme iron enzyme adsorbed on a silver colloid: a surface-enhanced resonance Raman scattering study. Broderick, J.B., Natan, M.J., O'Halloran, T.V., Van Duyne, R.P. Biochemistry (1993) [Pubmed]
  3. 4,5,6,7-Tetrachlorobenzo[d][1,3,2]dioxaborol- 2-ol as an Effective Catalyst for the Amide Condensation of Sterically Demanding Carboxylic Acids. Maki, T., Ishihara, K., Yamamoto, H. Org. Lett. (2006) [Pubmed]
  4. Characterisation of a chromosomally encoded catechol 1,2-dioxygenase (E.C. 1.13.11.1) from Alcaligenes eutrophus CH34. Sauret-Ignazi, G., Gagnon, J., Béguin, C., Barrelle, M., Markowicz, Y., Pelmont, J., Toussaint, A. Arch. Microbiol. (1996) [Pubmed]
  5. Oxidation kinetics of pentachlorophenol by manganese dioxide. Zhao, L., Yu, Z., Peng, P., Huang, W., Feng, S., Zhou, H. Environ. Toxicol. Chem. (2006) [Pubmed]
  6. A novel catabolic activity of Pseudomonas veronii in biotransformation of pentachlorophenol. Nam, I.H., Chang, Y.S., Hong, H.B., Lee, Y.E. Appl. Microbiol. Biotechnol. (2003) [Pubmed]
  7. Chlorinated benzo-1,2-quinones: an example of chemical transformation of toxicants during tests with aquatic organisms. Remberger, M., Hynning, P.A., Neilson, A.H. Ecotoxicol. Environ. Saf. (1991) [Pubmed]
 
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