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Mutagenicity induced in Salmonella strains TA98 and TA100 by diphenylthiophenes

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Warianty tytułu
Języki publikacji
EN
Abstrakty
EN
Mutagenic properties of four different diphenylthiophenes: 3,4-diphenylthiophene, 3,4-di(4'-methylphenyl)thiophene, 3,4-di(4'-methoxyphenyl)thiophene and 3,4-di(4'-pentoxyphenyl)thiophene were investigated applying the Salmonella test. The research was done on two strains of Salmonella Typhimurium: TA98 and TA100, tested in two variants: with (+S9) and without (-S9) enzymatic activation. Only one compound 3,4-di(4'-methylphenyl)thiophene showed mutagenic activity when studied with metabolic activation (+S9) and its mutagenic rate (MR) score was 3.41 for the dose of 10.00µg*plate-1. Other studied compounds did not show any mutagenic activity (+/-S9) and their MR score did not exceed the threshold value of 2.0.
Słowa kluczowe
Rocznik
Strony
65--69
Opis fizyczny
Bibliogr. 21 poz., tab., wykr.
Twórcy
autor
autor
autor
  • Department of Environmental Biotechnology, University of Warmia and Mazury in Olsztyn, Sloneczna 45G, 10-718 Olsztyn, Poland, kinga.budzikur@uwm.edu.pl
Bibliografia
  • Benigni, R., C. Bossa. 2008. Structure alerts for carcinogenicity, and the Salmonella assay system: A novel insight through the chemical relational databases technology. Mutation Research 695: 248-261.
  • Bressler, D.C., J.A. Norman, P.M. Fedorak. 1997. Ring cleavage of sulfur heterocycles: how does it happen? Biodegradation 8: 297-311.
  • Boctor, S., M.K. Ross, T. Salib, C.R. Shank. 1995. Modulation of DNA adduct formation by successive exposures of DNA to small and bulky chemical carcinogens. Carcinogenesis 16: 3057-3062.
  • Chadwick, D.J., J. Chambers, G.D. Meakins, R.L. Snowden. 1972. Preparation of thiophene esters by the Hinsberg reaction. Journal of the Chemical Society Perkin Transactions 1: 2079-2081.
  • Dang, Y., Y. Chen. 2007. Oxidation of 3,4-diaryl-2,5-dihydrothiophenes to 3,4-diarylthiophenes using CuBr2: Simple and efficient preparation of 3,4-diarylthiophenes. European Journal of Organic Chemistry 34: 5661-5666.
  • Dansette, M.P., G. Bertho, D. Mansuy. 2005. First evidence that cytochrome P450 may catalyze both S-oxidation and epoxidation of thiophene derivatives. Biochemical and Biophysical Research Communications 338: 450-455.
  • Dreiem, A., F. Fonnum. 2004. Thiophene is toxic to cerebellar granule cells in culture after bioactivation by rat liver enzymes. NeuroToxicology 25: 959-966.
  • Du, H., J. Wang, J. Watzl, X. Zhang, Z. Hu. 2008. Classification structure-activity relationship (CSAR) studies for prediction of genotoxicity of thiophene derivatives. Toxicology Letters 177: 10-19.
  • Grunwell, J.R., D.L. Foerst, M.J. Sanders. 1977. Mechanism of thiophene formation upon photolysis of enethiol esters. Journal of Organic Chemistry 42: 1142-1145.
  • Helgesen,M., F.C. Krebs. 2010. Photovoltaic performance of polymers based on dithienylthienopyrazines bearing thermocleavable benzoate esters. Macromolecules 43: 1253-1260.
  • Henckens, A., K. Colladet, S. Fourier, T.J. Cleij, L. Lutsen, J. Gelan, D. Vanderzande. 2005. Synthesis of 3,4-diphenyl-substituted poly(thienylene vinylene), low-band-gap polymers via the dithiocarbamate route. Macromolecules 38: 19-26.
  • Lin, H.L, H. Zhang, C. Medower, P.F. Hollenberg, W.W. Johnson. 2011. Inactivation of cytochrome P450 (P450) 3A4 but not P450 3A5 by OSI-930, a thiophene-containing anticancer drug. Drug Metabolism and Disposition 39: 345-350.
  • Maron, D.M., B.N. Ames. 1983. Revised methods for the Salmonella mutagenicity test. Mutation Research 113: 173-215.
  • Mortelmans, K., E. Zeiger. 2000. The Ames Salmonella/microsome mutagenicity assay. Mutation Research 455: 29-60.
  • Nakayama, J., H. Machina, M. Hoshino. 1985. General synthesis of 2,5-dihydrothiophenes (3-thiolenes) from diketo sulfides. Tetrahedron Letters 26: 1981-1982.
  • Odaci, D., S. Kiralp Kayahan, S. Timur, L. Toppare. 2008. Use of a thiophene-based conducting polymer in microbial biosensing. Electrochimica Acta 53: 4104-4108.
  • Ortiz de Montellano, P.R. 2005. Cytochrome P450: Structure, Mechanism and Biochemistry. 689 p. Kluwer Academic/Plenum Publishers, New York.
  • Perepichka, F.I, D.F. Perepichka. 2009. Handbook of Thiophene-Based Materiales vol 1: Synthesis and Theory. 865 p. John Wiley & Sons Ltd, Chichester, West Sussex.
  • Parvez, M., R.P. Jiminez, T.C. Sutherland, J. Viccars. 2009. Synthesis and optical and electronic properties of thiophene derivatives. European Journal of Organic Chemistry 32: 5635-5646.
  • Skotheim, T., J. Reynolds. 2007. Conjugated Polymers - Theory, Synthesis, Properties and Characterization. 992p. CRC Press. Boca Raton.
  • Speight, J.G. 1980. The Chemistry and Technology of Petroleum. 498p. Marcel Dekker Inc., New York.
Typ dokumentu
Bibliografia
Identyfikator YADDA
bwmeta1.element.baztech-article-BAR0-0066-0020
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