Please use this identifier to cite or link to this item: https://hdl.handle.net/11147/6268
Title: Synthesis, cytotoxic and antimicrobial activities of novel cobalt and zinc complexes of benzimidazole derivatives
Authors: Apohan, Elif
Yılmaz, Ülkü
Yılmaz, Özgür
Serindağ, Ayfer
Küçükbay, Hasan
Yeşilada, Özfer
Baran, Yusuf
Baran, Yusuf
Izmir Institute of Technology. Molecular Biology and Genetics
Keywords: Antimicrobial
Benzimidazole complexes
Cytotoxicity
Lung cancer
Issue Date: Jan-2017
Publisher: Elsevier Ltd.
Source: Apohan, E. ,Yılmaz, Ü., Yılmaz, Ö., Serindağ, A., Küçükbay, H., Yeşilada, Ö., and Baran, Y. (2017). Synthesis, cytotoxic and antimicrobial activities of novel cobalt and zinc complexes of benzimidazole derivatives. Journal of Organometallic Chemistry, 828, 52-58. doi:10.1016/j.jorganchem.2016.11.020
Abstract: In this study fourteen novel cobalt (II) or zinc (II) complexes of benzimidazoles were synthesized from the 1-(4-substitutedbenzyl)-1H-benzimidazoles and CoCl2·6H2O or ZnCl2. Cytotoxic activities of novel complexes were investigated against lung cancer cells (A549) and BEAS-2B. Three of the examined compounds (1, 4 and 5) showed high cytotoxic activity against A549. While the IC50 of the cisplatin was 2.56 μg/mL for A549 cells at 72 h, the IC50 values of compounds 1, 4 and 5 were 1.97, 1.87 and 1.9 μg/mL, respectively. IC50 values of these compounds for BEAS-2B cells were higher than the IC50 values for A549. While the IC50 values for BEAS-2B cells were 59.8, 24.5 and 32.67 μg/mL, respectively, the IC50 of the cisplatin was determined as 2.53 μg/mL in the present work. Three of the compounds have also high antimicrobial activity against all the microorganisms used.
URI: http://doi.org/10.1016/j.jorganchem.2016.11.020
http://hdl.handle.net/11147/6268
ISSN: 0022-328X
Appears in Collections:Molecular Biology and Genetics / Moleküler Biyoloji ve Genetik
Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection
WoS İndeksli Yayınlar Koleksiyonu / WoS Indexed Publications Collection

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