Design, Synthesis and Cytotoxicity Evaluationof New 1,2-diaryl-4, 5, 6, 7-Tetrahydro-1H-benzo[<i>d</i>] Imidazolesas Tubulin Inhibitors
| Author | Marzieh Amirmostofian | en |
| Author | Farzad Kobarfard | en |
| Author | Hamed Reihanfard | en |
| Author | Vida Mashayekhi | en |
| Author | Afshin Zarghi | en |
| Issued Date | 2015-01-31 | en |
| Abstract | A new series of 1,2-diaryl-4,5,6,7-tetrahydro-1H-benzo[d]imidazoles, possessing trimethoxyphenyl pharmacophore, were synthesized to evaluate their biological activities as tubulin inhibitors. Cytotoxic activity of the synthesized compounds 7a-f was assessed against several human cancer cell lines, including MCF-7 (breast cancer cell), HEPG2 (liver hepatocellular cells), A549 (adenocarcinomic human alveolar basal epithelial cells), T47D (Human ductal breast epithelial tumor cell line) and fibroblast. According to our results, HEPG2 seems to be the most sensitive, while MCF7 was the most resistant cell line to the compounds. All the compounds expect 7b, possessed satisfactory activity against HEPG2 with mean IC50 values ranging from 15.60 to 43.81 µM. | en |
| DOI | https://doi.org/10.22037/ijpr.2015.1627 | en |
| Keyword | 4 | en |
| Keyword | 5 | en |
| Keyword | 6 | en |
| Keyword | 7-Tetrahydro-1H-benzo[d]imidazole | en |
| Keyword | Antitubulin | en |
| Keyword | Molecular modeling | en |
| Keyword | Cytotoxicity | en |
| Publisher | Brieflands | en |
| Title | Design, Synthesis and Cytotoxicity Evaluationof New 1,2-diaryl-4, 5, 6, 7-Tetrahydro-1H-benzo[<i>d</i>] Imidazolesas Tubulin Inhibitors | en |
| Type | Original Article | en |
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