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Eur J Med Chem ; 46(9): 4366-73, 2011 Sep.
Article in English | MEDLINE | ID: mdl-21802797

ABSTRACT

Novel tricyclic carbazoles 4a-k were synthesized in one-pot employing sydnone derivatives 3a-k as masked hydrazines by the ring transformation in presence of conc. HCl and cyclohexanone. The title compounds were screened for anti-tubercular, anti cancer, DNA cleavage, antioxidant activity. MIC, GI50, LC50, TGI were evaluated. The title compounds have exhibited significant antitubercular, DNA cleavage and antioxidant activities and partial anticancer activity.


Subject(s)
Carbazoles/chemical synthesis , Carbazoles/pharmacology , DNA/chemistry , Pyrazoles/chemical synthesis , Pyrazoles/pharmacology , Antineoplastic Agents/chemical synthesis , Antineoplastic Agents/chemistry , Antineoplastic Agents/pharmacology , Antioxidants/chemical synthesis , Antioxidants/chemistry , Antioxidants/pharmacology , Antitubercular Agents/chemical synthesis , Antitubercular Agents/chemistry , Antitubercular Agents/pharmacology , Carbazoles/chemistry , Cell Line, Tumor , Gas Chromatography-Mass Spectrometry , Humans , Magnetic Resonance Spectroscopy , Mass Spectrometry , Microbial Sensitivity Tests , Pyrazoles/chemistry , Spectroscopy, Fourier Transform Infrared
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