2-2--azino-di-(3-ethylbenzothiazoline)-6-sulfonic-acid and Carcinoma

2-2--azino-di-(3-ethylbenzothiazoline)-6-sulfonic-acid has been researched along with Carcinoma* in 1 studies

Other Studies

1 other study(ies) available for 2-2--azino-di-(3-ethylbenzothiazoline)-6-sulfonic-acid and Carcinoma

ArticleYear
Complex formation, thermal behavior and stability competition between Cu(II) ion and Cu(0) nanoparticles with some new azo dyes. Antioxidant and in vitro cytotoxic activity.
    Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 2013, Apr-15, Volume: 107

    Four triazole and thiadiazole-based azo chromophores namely [(E)-4-((1H-1,2,4-triazol-3-yl)diazenyl)benzene-1,3-diol.(HL(1)), (E)-4-((5-(methylthio)-1H-1,2,4-triazol-3-yl)diazenyl)benzene-1,3-diol.(HL(2)), (E)-4-((1,3,4-thiadiazol-2-yl)diazenyl)benzene-1,3-diol.(HL(3)) and (E)-4-((5-mercapto-1,3,4-thiadiazol-2-yl)diazenyl)benzene-1,3-diol.(HL(4))] were synthesized and characterized by elemental analyses, IR, UV-Vis as well as mass spectroscopy. Cu(II) complexes of the investigated azo dyes have been synthesized and characterized by elemental analyses, IR, electronic and ESR spectra, magnetic susceptibility and thermogravimetric analyses. The bond lengths and bond angles have been calculated to confirm the geometry of the ligands and their Cu(II) complexes. The mode of interaction of the azodyes to copper nanoparticles was described as coordination mode of charged dye molecules on the colloidal Cu(0) surface through anchoring OH(-) group. The apparent association constants of the colloidal copper nanoparticles azodye complexes in solution were evaluated using the spectral method and compared with the formation constant of the Cu(II) azo complexes. The antitumor and antioxidant activities of the synthesized azo dyes and their Cu(II) azo complexes have been evaluated.

    Topics: Animals; Antineoplastic Agents; Antioxidants; Azo Compounds; Benzothiazoles; Carcinoma; Coloring Agents; Coordination Complexes; Copper; Female; Mice; Nanoparticles; Spectrum Analysis; Sulfonic Acids; Thiadiazoles; Triazoles

2013