The world's first wiki where authorship really matters (Nature Genetics, 2008). Due credit and reputation for authors. Imagine a global collaborative knowledge base for original thoughts. Search thousands of articles and collaborate with scientists around the globe.

wikigene or wiki gene protein drug chemical gene disease author authorship tracking collaborative publishing evolutionary knowledge reputation system wiki2.0 global collaboration genes proteins drugs chemicals diseases compound
Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)
 
Chemical Compound Review

Nitrosophenol     4-nitrosophenol

Synonyms: Quinone oxime, CHEMBL104353, NSC-3124, ACMC-1BVF6, CCRIS 4710, ...
 
 
Welcome! If you are familiar with the subject of this article, you can contribute to this open access knowledge base by deleting incorrect information, restructuring or completely rewriting any text. Read more.
 

High impact information on Quinone oxime

 

Anatomical context of Quinone oxime

 

Associations of Quinone oxime with other chemical compounds

 

Analytical, diagnostic and therapeutic context of Quinone oxime

  • The enzyme as it was prepared was colorless, but, after oxidation with p-nitrosophenol followed by gel filtration in the absence of NADH, it showed the absorption spectrum of a flavoprotein [9].

References

  1. Oxidation of phenylhydroxylamine in aqueous solution: a model for study of the carcinogenic effect of primary aromatic amines. Becker, A.R., Sternson, L.A. Proc. Natl. Acad. Sci. U.S.A. (1981) [Pubmed]
  2. Mechanism of p-nitrosophenol reduction catalyzed by horse liver and human pi-alcohol dehydrogenase (ADH). Human pi-ADH as a quinone reductase. Maskos, Z., Winston, G.W. J. Biol. Chem. (1994) [Pubmed]
  3. Catalysis of nitrosation in vitro and in vivo in rats by catechin and resorcinol and inhibition by chlorogenic acid. Pignatelli, B., Bereziat, J.C., Descotes, G., Bartsch, H. Carcinogenesis (1982) [Pubmed]
  4. Nitrosation by peroxynitrite: use of phenol as a probe. Uppu, R.M., Lemercier, J.N., Squadrito, G.L., Zhang, H., Bolzan, R.M., Pryor, W.A. Arch. Biochem. Biophys. (1998) [Pubmed]
  5. p-nitrosophenol reduction by liver cytosol from ADH-positive and -negative deermice (Peromyscus maniculatus). Dudley, B.F., Winston, G.W. Arch. Biochem. Biophys. (1995) [Pubmed]
  6. Correlation between fluidising effects on phospholipid membranes and mitochondrial respiration of propofol and p-nitrosophenol homologues. Momo, F., Fabris, S., Wisniewska, A., Fiore, C., Bindoli, A., Scutari, G., Stevanato, R. Biophys. Chem. (2003) [Pubmed]
  7. New aspects in the reaction mechanism of phenol with peroxynitrite: the role of phenoxy radicals. Daiber, A., Mehl, M., Ullrich, V. Nitric Oxide (1998) [Pubmed]
  8. Formation of a mutagenic diazoquinone by interaction of phenol with nitrite. Kikugawa, K., Kato, T. Food Chem. Toxicol. (1988) [Pubmed]
  9. Studies on the enzymatic reduction of C-nitroso compounds. V. Molecular properties of porcine heart C-nitrosoreductase and identity of this enzyme with NAD(P)H dehydrogenase. Horie, S., Watanabe, T., Ohta, A. J. Biochem. (1982) [Pubmed]
 
WikiGenes - Universities