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

o-Jodfenol     2-iodophenol

Synonyms: o-Jodphenol, o-Iodophenol, PubChem3963, SureCN5720, CHEMBL225564, ...
 
 
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 o-Jodphenol

  • On the other hand, the intramolecular cyclization of the prenyl ether of 2-iodophenol would proceed in a fashion similar to the conventional palladium-catalyzed transformation [1].
  • Inhibitors of the reaction catalyzed by TS PST, including 2,6-dichloro-4-nitrophenol-3'-phosphoadenosine- 5'-phosphate and NaCl, as well as 2-iodophenol, a competing substrate, inhibited the photolabeling of both of these proteins by [125I]IAP in a concentration-dependent fashion [2].
  • Intermediate and mechanism of hydroxylation of o-iodophenol by salicylate hydroxylase [3].
 

Biological context of o-Jodphenol

 

Associations of o-Jodphenol with other chemical compounds

References

  1. Cobalt-catalyzed trimethylsilylmethylmagnesium-promoted radical alkenylation of alkyl halides: A complement to the Heck reaction. Affo, W., Ohmiya, H., Fujioka, T., Ikeda, Y., Nakamura, T., Yorimitsu, H., Oshima, K., Imamura, Y., Mizuta, T., Miyoshi, K. J. Am. Chem. Soc. (2006) [Pubmed]
  2. Human liver thermostable phenol sulfotransferase: photoaffinity labeling with 2-iodo-4-azidophenol. Otterness, D.M., Powers, S.P., Miller, L.J., Weinshilboum, R.M. Mol. Pharmacol. (1989) [Pubmed]
  3. Intermediate and mechanism of hydroxylation of o-iodophenol by salicylate hydroxylase. Suzuki, K., Gomi, T., Itagaki, E. J. Biochem. (1991) [Pubmed]
  4. Hydroxylation of o-halogenophenol and o-nitrophenol by salicylate hydroxylase. Suzuki, K., Gomi, T., Kaidoh, T., Itagaki, E. J. Biochem. (1991) [Pubmed]
 
WikiGenes - Universities