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5th World Congress on Cancer Therapy

Atlanta, USA

Mine Yarim

Yeditepe University, Turkey

Title: Synthesis and preliminary mechanistic evaluation of N-(Substituted-1,3-Benzothiazol-2-yl)-2- (4-Substituted-Piperazin-1-yl) Acetamide derivatives with potent antiproliferative activity on human cancer cell lines


Biography: Mine Yarim


This lecture will cover synthesis, characterization and cytotoxic activities of some new benzothiazole-piperazine derivatives. Structures of compounds N-(substituted-1,3-benzothiazol-2-yl)-2-(4-substituted-piperazin-1-yl)acetamide derivatives were clarifi ed with IR, 1H-NMR, 13C-NMR, mass spectroscopies and elemental analyses. In vitro cytotoxic activities of compounds were screened against hepatocellular (HUH-7), breast (MCF-7) and colorectal (HCT-116) cancer cell lines by sulphorhodamine B assay. Based on the GI50 values of the compounds, most of the benzothiazole-piperazine derivatives are active against HUH-7, MCF-7 and HCT-116 cancer cell lines. In addition, further investigation of compounds by Hoechst staining and FACS revealed that these compounds cause apoptosis by cell cycle arrest at subG1 phase. On the basis of their high potency in cellular environment, these straightforward benzothiazole-piperazine derivatives may possess potential in the design of more potent compounds for intervention with cancer cell proliferation.