Ranganatha, S. R. and Kavitha, C. V. and Vinaya, K. and Prasanna, D. S. and Chandrappa, S. and Sathees Raghavan, C. and Rangappa, K. S. (2009) Synthesis and cytotoxic evaluation of novel 2-(4-(2,2,2-trifluoroethoxy)-3-methylpyridin-2-ylthio)-1H-benzodimidazole derivatives. Archives of Pharmacal Research, 32 (10). pp. 1335-1343. ISSN 1976-3786
Full text not available from this repository. (Request a copy)Abstract
The present work deals with the anticancer effect of benzimidazole derivatives associated with the pyridine framework. By varying the functional group at N-terminal of the benzimidazole by different L-amino acids, several 2-(4-(2,2,2-trifluoroethoxy)-3-methylpyridin-2-ylthio)-1Hbenzo[d]imidazole derivatives 9(a-j) were synthesized. Their chemical structures were confirmed by 1H NMR, IR and mass spectroscopic techniques. The synthesized compounds were examined for their antiproliferative effects against human leukemia cell lines, K562 and CEM. The preliminary results showed most of the derivatives had moderate antitumor activity. Compound 9j containing cysteine residue exhibited good inhibition compared to other amino acid resides. In addition DNA fragmentation results suggest that 9j is more cytotoxic and able to induce apoptosis.
| Item Type: | Article |
|---|---|
| Uncontrolled Keywords: | Benzimidazole and Amino Acids and Cytotoxicity and Chronic Myelogenous Leukemia |
| Subjects: | C Chemical Science > Chemistry |
| Divisions: | Department of > Chemistry |
| Depositing User: | Users 19 not found. |
| Date Deposited: | 04 Sep 2019 05:44 |
| Last Modified: | 04 Sep 2019 05:44 |
| URI: | http://eprints.uni-mysore.ac.in/id/eprint/7504 |
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