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

Diaminobenzene     benzene-1,3-diamine

Synonyms: m-Aminoaniline, Developer C, Developer H, Developer M, Developer 11, ...
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 APCO 2330


High impact information on APCO 2330


Chemical compound and disease context of APCO 2330


Biological context of APCO 2330


Anatomical context of APCO 2330


Associations of APCO 2330 with other chemical compounds


Gene context of APCO 2330

  • These potential shifts represent 23 and 17 kJ/mol stabilization of the monolayers modified by 1,4- and 1,3-phenylenediamine, respectively [17].
  • m-Phenylenediamine (m-PDA, CAS: 108-45-2), a component of hair-dye formulations, was administered in the drinking-water to groups of female and male (C57BL/6 x C3H/He)F1 (B6C3F1) mice at concentrations of 0.02 or 0.04% for 78 wk [18].

Analytical, diagnostic and therapeutic context of APCO 2330


  1. Regulation of melanin production by Cryptococcus neoformans. Nurudeen, T.A., Ahearn, D.G. J. Clin. Microbiol. (1979) [Pubmed]
  2. Mutagens in rat urine after dermal application of 1,3-diaminobenzene. Clemmensen, S., Lam, H.R. Mutat. Res. (1984) [Pubmed]
  3. Mutagenicity of commercial hair dyes and detection of 2,7-diaminophenazine. Watanabe, T., Hirayama, T., Fukui, S. Mutat. Res. (1990) [Pubmed]
  4. In vivo brain glucose measurements: differential normal pulse voltammetry with enzyme-modified carbon fiber microelectrodes. Netchiporouk, L.I., Shram, N.F., Jaffrezic-Renault, N., Martelet, C., Cespuglio, R. Anal. Chem. (1996) [Pubmed]
  5. Pigment production by Cryptococcus neoformans and other Cryptococcus species from aminophenols and diaminobenzenes. Chaskes, S., Tyndall, R.L. J. Clin. Microbiol. (1978) [Pubmed]
  6. Plant activation of aromatic amines mediated by cytochromes P450 and flavin-containing monooxygenases. Chiapella, C., Radovan, R.D., Moreno, J.A., Casares, L., Barbé, J., Llagostera, M. Mutat. Res. (2000) [Pubmed]
  7. DNA damage induced by m-phenylenediamine and its derivative in the presence of copper ion. Chen, F., Murata, M., Hiraku, Y., Yamashita, N., Oikawa, S., Kawanishi, S. Free Radic. Res. (1998) [Pubmed]
  8. The mutagenic modulating effect of p-phenylenediamine on the oxidation of o- or m-phenylenediamine with hydrogen peroxide in the Salmonella test. Watanabe, T., Hirayama, T., Fukui, S. Mutat. Res. (1990) [Pubmed]
  9. Genotoxicity of m-phenylenediamine and 2-aminofluorene in Salmonella typhimurium and human lymphocytes with and without plant activation. Plewa, M.J., Wagner, E.D., Yu, T.W., Anderson, D. Environ. Mol. Mutagen. (1995) [Pubmed]
  10. Mutagenic synergy between paraoxon and mammalian or plant-activated aromatic amines. Wagner, E.D., Repetny, K., Tan, J.S., Gichner, T., Plewa, M.J. Environ. Mol. Mutagen. (1997) [Pubmed]
  11. Metabolic activation of m-phenylenediamine to products mutagenic in Salmonella typhimurium by medium isolated from tobacco suspension cell cultures. Gichner, T., Stavreva, D.A., Cerovská, N., Wagner, E.D., Plewa, M.J. Mutat. Res. (1995) [Pubmed]
  12. Structure-activity relationship within a series of m-diaminobenzene derivatives. Shahin, M.M., Bugaut, A., Kalopissis, G. Mutat. Res. (1980) [Pubmed]
  13. Plant activation of m-phenylenediamine by tobacco, cotton, and carrot cell suspension cultures. Lhotka, M.A., Plewa, M.J., Gentile, J.M. Environ. Mol. Mutagen. (1987) [Pubmed]
  14. The plant activation of m-phenylenediamine by Tradescantia clone 03 and clone 4430 cells in liquid suspension culture. Anderson, V.A., Plewa, M.J., Gentile, J.M. Mutat. Res. (1988) [Pubmed]
  15. Evaluation of cross-sensitization among dye-intermediate agents using a modified lymphocyte transformation test. Li, Q., Inagaki, H., Minami, M. Arch. Toxicol. (1996) [Pubmed]
  16. Amperometric biosensor with HRP immobilized on a sandwiched nano-Au / polymerized m-phenylenediamine film and ferrocene mediator. Li, J., Xiao, L.T., Liu, X.M., Zeng, G.M., Huang, G.H., Shen, G.L., Yu, R.Q. Analytical and bioanalytical chemistry. (2003) [Pubmed]
  17. Reductive desorption of 11-mercaptoundecanoic acid monolayers modified by covalent attachment of 1,3- and 1,4-phenylenediamine. Anderson, M.R., Baltzersen, R. Journal of colloid and interface science. (2003) [Pubmed]
  18. Carcinogenicity and toxicity study of m-phenylenediamine administered in the drinking-water to (C57BL/6 x C3H/He)F1 mice. Amo, H., Matsuyama, M., Amano, H., Yamada, C., Kawai, M., Miyata, N., Nakadate, M. Food Chem. Toxicol. (1988) [Pubmed]
  19. Ferrocene-conjugated m-phenylenediamine conducting polymer-incorporated peroxidase biosensors. Mulchandani, A., Pan, S. Anal. Biochem. (1999) [Pubmed]
  20. Characterization of a macromolecular matrix isolated from tobacco suspension cell cultures and its role in the activation of promutagenic m-phenylenediamine. Stavreva, D.A., Wagner, E.D., Plewa, M.J., Gichner, T. Mutat. Res. (1997) [Pubmed]
  21. Mutagenicity of nitro- and amino-substituted phenazines in Salmonella typhimurium. Watanabe, T., Hanasaki, Y., Hirayama, T., Fukui, S. Mutat. Res. (1989) [Pubmed]
  22. Host-guest complexation in capillary isotachophoresis. II. Determination of aminophenol and diaminobenzene isomers in permanent hair colorants by using capillary isotachophoresis. Fanali, S. J. Chromatogr. (1989) [Pubmed]
WikiGenes - Universities