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New compounds based on a benzimidazole nucleus: synthesis, characterization and cytotoxic activity against breast and colon cancer cell lines

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dc.creator Akkoc, Senem
dc.creator Kayser, Veysel
dc.creator Hawkins, Bryson
dc.creator Williams, Peter A.
dc.creator Hibbs, David E.
dc.creator Lai, Felcia
dc.creator GÖK, YETKİN
dc.creator İLHAN, İLHAN ÖZER
dc.date 2017-06-14T21:00:00Z
dc.date.accessioned 2020-10-06T12:02:52Z
dc.date.available 2020-10-06T12:02:52Z
dc.identifier f897321b-bc21-4b2b-b711-c26abb448de0
dc.identifier 10.1016/j.jorganchem.2017.03.037
dc.identifier https://avesis.sdu.edu.tr/publication/details/f897321b-bc21-4b2b-b711-c26abb448de0/oai
dc.identifier.uri http://acikerisim.sdu.edu.tr/xmlui/handle/123456789/76607
dc.description Benzimidazolium salts and their Pyridine Enhanced Precatalyst Preparation Stabilization and Initiation (PEPPSI) palladium N-heterocyclic carbene (Pd-NHC) based complexes have been synthesized and their structures characterized with a number of different instrumental techniques including NMR (H-1 and C-13), IR, EI-MS (for 2), X-ray (for 1, 2 and 4) and elemental analysis. The cytotoxicity of all the compounds was tested using the human embryonic kidney (HEK-293T), human breast epithelial adenocarcinoma (MDA-MB-231), and human colon epithelial colorectal adenocarcinoma (DLD-1) cell lines. The benzimidazolium salts (2-5) had more cytotoxic activity against cancerous cells compared with the metal complexes (6-9), which curiously exhibited no activity against any of the cell lines. Based on the IC50 values, compound 5 displayed the highest in vitro anticancer activity among compounds 2-9. Crown Copyright (C) 2017 Published by Elsevier B.V. All rights reserved.
dc.language eng
dc.rights info:eu-repo/semantics/closedAccess
dc.title New compounds based on a benzimidazole nucleus: synthesis, characterization and cytotoxic activity against breast and colon cancer cell lines
dc.type info:eu-repo/semantics/article


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