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

Diphenyl urea     1,1-diphenylurea

Synonyms: SureCN75883, SureCN75885, CHEMBL169502, NSC-8715, CCRIS 4635, ...
 
 
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.
 

Disease relevance of NSC8715

 

High impact information on NSC8715

  • Activation of human ether-a-go-go-related gene potassium channels by the diphenylurea 1,3-bis-(2-hydroxy-5-trifluoromethyl-phenyl)-urea (NS1643) [2].
  • Computational docking experiments indicate how diphenylurea compounds bind to the plasmepsin active site and inhibit the enzyme [3].
  • Here we further show that AHK4 is a primary receptor that directly binds a variety of natural and synthetic cytokinins (e.g. not only N(6)-substituted aminopurines such as isopentenyl-adenine, trans-zeatin, benzyl-adenine, but also diphenylurea derivatives such as thidiazuron), in a highly specific manner (K(d) = 4.55+/-0.48x10(-9) M) [4].
  • Some widely used standard protocols for the separation of phenylthiohydantoin amino acid derivatives by reverse-phase gradient HPLC do not provide separation of the phenylthiohydantoin derivative of tryptophan (PTH-Trp) from diphenylurea (DPU), a by-product generated during Edman degradation of proteins in variable amounts [5].

References

  1. Quantitative structure activity relationship in diphenyl ureas for insect growth regulating activity. George, N., Vasuki, V. Indian J. Med. Res. (1991) [Pubmed]
  2. Activation of human ether-a-go-go-related gene potassium channels by the diphenylurea 1,3-bis-(2-hydroxy-5-trifluoromethyl-phenyl)-urea (NS1643). Hansen, R.S., Diness, T.G., Christ, T., Demnitz, J., Ravens, U., Olesen, S.P., Grunnet, M. Mol. Pharmacol. (2006) [Pubmed]
  3. New class of small nonpeptidyl compounds blocks Plasmodium falciparum development in vitro by inhibiting plasmepsins. Jiang, S., Prigge, S.T., Wei, L., Gao Ye, n.u.l.l., Hudson, T.H., Gerena, L., Dame, J.B., Kyle, D.E. Antimicrob. Agents Chemother. (2001) [Pubmed]
  4. The Arabidopsis AHK4 histidine kinase is a cytokinin-binding receptor that transduces cytokinin signals across the membrane. Yamada, H., Suzuki, T., Terada, K., Takei, K., Ishikawa, K., Miwa, K., Yamashino, T., Mizuno, T. Plant Cell Physiol. (2001) [Pubmed]
  5. A method for the unambiguous identification of tryptophan in automated protein sequence analysis. Müller-Michel, T., Böhlen, P. Anal. Biochem. (1990) [Pubmed]
 
WikiGenes - Universities