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

INDOPHENOL     4-(4- hydroxyphenyl)iminocyclohexa- 2,5-dien...

Synonyms: SureCN35153, AG-F-68019, CHEBI:50428, I5763_SIGMA, KB-52688, ...
 
 
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 INDOPHENOL

 

High impact information on INDOPHENOL

  • We show that an indophenol-based colorimetric method for acetaminophen (Clin Toxicol 15: 67-73, 1979) has less than maximal sensitivity because of (a) incomplete hydrolysis, related to suboptimal acid concentration; (b) suboptimal hydrolysis time; and (c) possible deterioration of the ammonium hydroxide reagent after 2.5 months [4].
  • A sensitive, optimized assay for serum AMP deaminase (EC 3.5.4.6) is presented, which is based on a colorimetric indophenol determination of ammonia liberated during the enzyme reaction [5].
  • These isolates were gram-negative, oxidative rods which were motile by means of a single polar flagellum; gave positive catalase, indophenol oxidase, urease, and amylase reactions; and grew slowly at 30 degrees C. Fourteen isolates conformed to the designated type strains Pseudomonas mesophilica ATCC 29983 and Protaminobacter ruber ATCC 8457 [6].
  • Two isolates of Pseudomonas aeruginosa lacking characteristic indophenol oxidase were recovered from a sputum specimen [7].
  • 2,6-Dichloro-phenol indophenol prevents switch-over of electrons between the cyanide-sensitive and -insensitive pathway of the mitochondrial electron transport chain in the presence of inhibitors [8].
 

Biological context of INDOPHENOL

 

Anatomical context of INDOPHENOL

 

Associations of INDOPHENOL with other chemical compounds

 

Gene context of INDOPHENOL

  • Urea produced by arginase was hydrolyzed to ammonia by urease, the ammonia was converted to indophenol, and the absorbance was measured at 570 nm [16].
  • In reverse micelles, some inhibitors of AChE (propidium, and d-tubocurarine) have much less effect upon indophenol-acetate hydrolysis than they do in a dilute solution environment [17].
 

Analytical, diagnostic and therapeutic context of INDOPHENOL

  • Analysis is carried out in end-point samples by Winkler's titration and indophenol-blue for oxygen and ammonia-N, respectively [18].

References

  1. Isolation of oxidase-negative Pseudomonas aeruginosa from urine culture. McCleskey, F.K., Adams, E.D. J. Clin. Microbiol. (1980) [Pubmed]
  2. Arterial ammonia with Blood Ammonia Checker II and with indophenol reaction to assess presence of hepatic encephalopathy. Huizenga, J.R., van Dam, G.M., Gips, C.H. Clin. Chim. Acta (1996) [Pubmed]
  3. Plesiomonas (Aeromonas) shigelloides septicemia and meningitis in a neonate. Dahm, L.J., Weinberg, A.G. South. Med. J. (1980) [Pubmed]
  4. Indophenol method for acetaminophen in serum examined. Novotny, P.E., Elser, R.C. Clin. Chem. (1984) [Pubmed]
  5. Sensitive, optimized assay for serum AMP deaminase. Pedersen, R.C., Berry, A.J. Clin. Chem. (1977) [Pubmed]
  6. Pseudomonas mesophilica and an unnamed taxon, clinical isolates of pink-pigmented oxidative bacteria. Gilardi, G.L., Faur, Y.C. J. Clin. Microbiol. (1984) [Pubmed]
  7. Isolation of oxidase-negative Pseudomonas aeruginosa from sputum culture. Hampton, K.D., Wasilauskas, B.L. J. Clin. Microbiol. (1979) [Pubmed]
  8. 2,6-Dichloro-phenol indophenol prevents switch-over of electrons between the cyanide-sensitive and -insensitive pathway of the mitochondrial electron transport chain in the presence of inhibitors. Kumar, S., Acharya, S.K. Anal. Biochem. (1999) [Pubmed]
  9. Multilocus enzyme analysis of the genus Aeromonas and its use for species identification. Altwegg, M., Reeves, M.W., Altwegg-Bissig, R., Brenner, D.J. Zentralbl. Bakteriol. (1991) [Pubmed]
  10. The role of chloride ion on the photoreactivation of the oxygen-evolving center of tris-washed, 2,6-dichlorophenol indophenol-treated grana. Yamashita, T., Ashizawa, A. Arch. Biochem. Biophys. (1985) [Pubmed]
  11. Determination of ammonia in cerebrospinal fluid using the indophenol direct method. Huizenga, J.R., Teelken, A.W., Tangerman, A., de Jager, A.E., Gips, C.H., Jansen, P.L. Mol. Chem. Neuropathol. (1998) [Pubmed]
  12. Redox reactions of tonoplast and plasma membranes isolated from soybean hypocotyls by free-flow electrophoresis. Barr, R., Sandelius, A.S., Crane, F.L., Morré, D.J. Biochim. Biophys. Acta (1986) [Pubmed]
  13. Spectrophotometric determination of oxyphenbutazone in drug formulations using the indophenol reaction. Verma, K.K., Jain, A. The Analyst. (1985) [Pubmed]
  14. Assays for allantoinase. Romanov, V., Merski, M.T., Hausinger, R.P. Anal. Biochem. (1999) [Pubmed]
  15. Sensitivity improvement of ammonia determination based on flow-injection indophenol spectrophotometry with manganese(II) ion as a catalyst and analysis of exhaust gas of thermal power plant. Tsuboi, T., Hirano, Y., Shibata, Y., Motomizu, S. Analytical sciences : the international journal of the Japan Society for Analytical Chemistry. (2002) [Pubmed]
  16. Assay and kinetics of arginase. Garganta, C.L., Bond, J.S. Anal. Biochem. (1986) [Pubmed]
  17. Reverse-micelle model: pH, electromagnetic field and inhibitor enzyme interaction. Chattopadhyay, S.K., Toews, K.A., Butt, S., Barlett, R., Brown, H.D. Cancer Biochem. Biophys. (1997) [Pubmed]
  18. Simultaneous measurements of oxygen consumption and ammonia-N excretion in embryos and larvae of marine invertebrates. Lemos, D., Jorge, R.L., Phan, V.N. Comp. Biochem. Physiol., Part A Mol. Integr. Physiol. (2003) [Pubmed]
 
WikiGenes - Universities