Design, synthesis, characterization and pharmacological screening of some novel 2 substituted and 1(h)-substituted Benzimidazole derivatives
Keywords:
benzimidazole, anticancer, QSAR, characterization, pharmacologoical activityAbstract
The most of drugs containing Benzimidazole ring is a prominent structural motif found in numerous therapeutically active compounds. Benzimidazole and its synthetic analogues have been found to exhibit industrial, agricultural and biological application such asantitubercular, anti-inflammatory, analgesic, anticancer, anticoagulant, as well as good antifungal and anti microbial activity.Recent advances in technology considers microwave irradiation energy as the most efficient means of heating reactions for chemical transformations that can be accomplished in a minutes. Microwave irradiation assists organic synthesis (MAOS) not only help in implementing green chemistry but also led to progress in organic synthesis. We report pharmacological screening of some novel 2 substituted and 1(h)-substituted Benzimidazole derivatives.
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References
Welsch, M. E.; Snyder, S. A.; Stockwell, B. R. Privileged Scaffolds for Library Design and Drug Discovery. Curr.Opin.Chem. Biol. (2010), 14, 347.
(a) Bansal, Y.; Silakari, O. The therapeutic journey of benzimidazoles.Bioorg.Med. Chem. (2012,) 20, 6208.
Hernandez-Luis, F.; Hernandez-Campos, A.; Castillo, R.; Navarrete-Vazquez, G.; Soria-Arteche, O.; Hernandez-Hernandez, M.; Yepez-Mulia, L. Synthesis and biological activity of 2-(trifluoromethyl)- 1H-benzimidazole derivatives against some protozoa and Tricheinellaspiralis. Eur. J. Med. Chem. (2010), 45, 3135.
Khalil, A. M.; Berghot, M. A.; Gouda, M. A. Synthesis and study of some new 1,3-isoinodoledione derivatives as potential antibacterial agents. Eur. J. Med. Chem. (2010), 45, 1552.
Kamal, A.; Ponnampalli, S.; Vishnuvardhan, M. V. P. S.; Rao, M. P. N.; Mullagiri, K.; Nayak, V. L.; Chandrakant, B. Synthesis of imidazothiadiazole-benzimidazole conjugates as mitochondrial apoptosis inducers. MedChemComm(2014), 5, 1644.
Saour, K.; Lafta, D. Synthesis of New Benzimidazoles and Benzothiazole Disulfide Metal Complexes as G-quadruplex Binding Ligands. Anti-Cancer Agents Med. Chem. (2016), 16, 891.
Zou, R.; Ayres, K. R.; Drach, J. C.; Townsend, L. B. Synthesis and Antiviral Evaluation of Certain Disubstituted Benzimidazole Ribonucleosides. J. Med. Chem. (1996), 39, 3477.
Chassaing, C.; Berger, M.; Heckeroth, A.; Ilg, T.; Jaeger, M.; Kern, C.; Schmid, K.; Uphoff, M. Highly Water-Soluble Prodrugs of Anthelmintic Benzimidazole Carbamates: Synthesis, Pharmacodynamics, and Pharmacokinetics. J. Med. Chem. (2008), 51, 1111.
Mavrova, A. T.; Yancheva, D.; Anastassova, N.; Anichina, K.; Zvezdanovic, J.; Djordjevic, A.; Markovic, D.; Smelcerovic, A. Synthesis, electronic properties, antioxidant and antibacterial activity of some new benzimidazoles. Bioorg.Med. Chem. (2015), 23, 6317.
Cereda, E.; Turconi, M.; Ezhaya, A.; Bellora, E.; Brambilla, A.; Pagani, F.; Donetti, A. Anti-secretory and ‘anti-ulcer activities of some new 2-(2-pyridylmethyl-sulfinyl)-benzimidazoles. Eur. J. Med. Chem. (1987), 22, 527.
Wang, J.-L.; Zhang, J.; Zhou, Z.-M.; Li, Z.-H.; Xue, W.-Z.; Xu, D.; Hao, L.-P.; Han, X.-F.; Fei, F.; Liu, T.; Liang, A.-H. Design, synthesis and biological evaluation of 6-substituted aminocarbonylbenzimidazole derivatives as nonpeptidic angiotensin II AT1 receptor antagonists. Eur. J. Med. Chem. (2012), 49, 183.
Hameed P, S.; Raichurkar, A.; Madhavapeddi, P.; Menasinakai, S.; Sharma, S.; Kaur, P.; Nandishaiah, R.; Panduga, V.; Reddy, J.; Sambandamurthy, V. K.; Sriram, D. Benzimidazoles: Novel Mycobacterial Gyrase Inhibitors from Scaffold Morphing. ACS Med. Chem. Lett. (2014), 5, 820.
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