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

Phenylazide     azidobenzene

Synonyms: Azidobenzene, azido-benzene, AGN-PC-00GIMI, Phenyl azide, AG-B-14344, ...
 
 
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 azidobenzene

  • Using phenyl-azide-mediated photocrosslinking, we show that the alpha carbon of amino acid 2 of the helix-turn-helix motif of bacteriophage lambda Cro is within 12 A of the bottom-strand nucleotides at positions 2 and 3 of the DNA half site in the Cro-DNA complex in solution [1].
 

High impact information on azidobenzene

  • A biologically active CT analogue, [Arg11,18, Lys14]sCT, derivatized with the photoreactive phenylazide cross-linking agent, N-hydroxysuccinimidyl-4-azidobenzoate, was used to identify receptor components of Mr approximately 88,000 and approximately 71,000 in both particulate placental membranes and the solubilized extract [2].
  • Specifically, two phr probes representing the 139-172 bp region of the MVM P4 promoter were constructed in which the highly phr phenylazide group was attached with a linker at nucleotide 168, towards the side of the GC box proximal to the TATA box [3].
  • The photoactivable compound phenylazide interacts reversibly with the frog's olfactory epithelium when delivered as an olfactory stimulus [4].
  • In bacteriorhodopsin, photoaffinity studies using a retinal with a C-10 tritiated phenylazide appended through a 13 A spacer cross-linked to Arg-175/Asn-176 on the cytoplasmic side of helix F; this indicates that 9-Me points toward the extracellular space [5].
  • Based on the photoreactive chemistry of a phenylazide group, a novel surface micropatterning technology for cultured cells was successfully developed [6].

References

  1. Phenyl-azide-mediated photocrosslinking analysis of Cro-DNA interaction. Chen, Y., Ebright, R.H. J. Mol. Biol. (1993) [Pubmed]
  2. Solubilization of functional calcitonin receptors. Nicholson, G.C., D'Santos, C.S., Evans, T., Moseley, J.M., Kemp, B.E., Martin, T.J. Biochem. J. (1988) [Pubmed]
  3. Localization of adjacent binding domains for cellular proteins over the minute virus of mice P4 promoter by site-specific photoaffinity labelling. Kumar, G., Sharma, A.K. Gene (1993) [Pubmed]
  4. Investigations of the discriminative properties of the frog's olfactory mucosa using a photoactivable odorant. Delaleu, J.C., Holley, A. Neurosci. Lett. (1983) [Pubmed]
  5. Photoaffinity labeling of rhodopsin and bacteriorhodopsin. Nakanishi, K., Zhang, H., Lerro, K.A., Takekuma, S., Yamamoto, T., Lien, T.H., Sastry, L., Baek, D.J., Moquin-Pattey, C., Boehm, M.F. Biophys. Chem. (1995) [Pubmed]
  6. Development of micropatterning technology for cultured cells. Matsuda, T., Inoue, K., Sugawara, T. ASAIO transactions / American Society for Artificial Internal Organs. (1990) [Pubmed]
 
WikiGenes - Universities