[
Andrzejewska M., L. Yepez-Mulia, A. Tapia, R. Cedillo-Rivera, A.E. Laudy, B.J. Starościak and Z. Kazimierczuk. 2004. Synthesis, and antiprotozoal and antibacterial activities of S-substituted 4,6-dibromo- and 4,6-dichloro-2-mercaptobenzimidazoles. Eur. J. Pharm. Sci. 21: 323–329.
]Search in Google Scholar
[
Bansal Y. and O. Silakari. 2012. The therapeutic journey of benzimidazoles: a review. Bioorg. Med. Chem. 20: 6208–6236.10.1016/j.bmc.2012.09.01323031649
]Search in Google Scholar
[
Gaba M., S. Singh and C. Mohan. 2014. Benzimidazole: an emerging scaffold for analgesic and anti-inflammatory agents. Eur. J. Med. Chem. 76: 494–505.10.1016/j.ejmech.2014.01.03024602792
]Search in Google Scholar
[
Gianoncelli A., G. Cozza, A. Orzeszko, F. Meggio, Z. Kazimier- czuk and L. A. Pinna. 2009. Tetraiodobenzimidazoles are potent inhibitors of protein kinase CK2. Bioorg. Med. Chem. 17: 7281–7289.10.1016/j.bmc.2009.08.04719748274]Search in Google Scholar
[
Horton D.A., G.T. Bourne and M. L. Smythe. 2003. The combinatorial synthesis of bicyclic privileged structures or privileged substructures. Chem. Rev. 103: 893–930.10.1021/cr020033s12630855
]Search in Google Scholar
[
Janeczko M., A. Orzeszko, Z. Kazimierczuk, R. Szyszka and A. Baier. 2012. CK2α and CK2α’ subunits differ in their sensitivity to 4,5,6,7-tetrabromo- and 4,5,6,7-tetraiodo-1H-benzimidazole derivatives. Eur. J. Med. Chem. 47: 345–350.
]Search in Google Scholar
[
Kaplancikli Z.A., G. Turan-Zitouni, G. Revial and K. Guven. 2004. Synthesis and study of antibacterial and antifungal activities of novel 2-[[(benzoxazole/benzimidazole-2-yl)sulfanyl] acetylamino] thiazoles. Arch. Pharm. Res. 27: 1081–1085.10.1007/BF0297510815595406
]Search in Google Scholar
[
Karpińka M.M., J. Matysiak and A. Niewiadomy. 2011 . Synthesis of novel 4-(1H-benzimidazol-2-yl)benzene-1,3-diols and their cytotoxic activity against human cancer cell lines. Arch. Pharm. Res. 34: 1639–1647.
]Search in Google Scholar
[
Karpińska M.M., J. Matysiak, A. Niewiadomy, J. Wietrzyk and D. Kłopotowska. 2012. Synthesis and biological activity of novel 4- and 6-(1-alkyl/aryl-1H-benzimidazol-2-yl)benzene-1,3-diols Mona tshefte für Chemie 143: 269–276.10.1007/s00706-011-0665-5
]Search in Google Scholar
[
Kazimierczuk Z., M. Andrzejewska, J. Kaustova and V. Klimesova. 2005. Synthesis and antimycobacterial activity of 2-substituted halogenobenzimidazoles. Eur. J. Med. Chem. 40: 203–208.10.1016/j.ejmech.2004.10.00415694655
]Search in Google Scholar
[
Küçükbay H., R. Durmaz, N. Okyucu and S. Günal. 2003a. Antifungal activity of some bis-5-methylbenzimidazole compounds. Folia Microbiol (Praha) 48: 679–681.10.1007/BF0299347814976728
]Search in Google Scholar
[
Küçükbay H., R. Durmaz, E. Orhan and S. Günal. 2003b. Synthesis, antibacterial and antifungal activities of electron-rich olefins derived benzimidazole compounds. Farmaco 58: 431–437.
]Search in Google Scholar
[
Laudy A.E., R. Moo-Puc, R. Cedillo-Rivera, Z. Kazimierczuk and A. Orzeszko. 2012. Synthesis and antimicrobial activities of new polyhalogenated benzimidazoles. Journal of Heterocyclic Chemistry 49: 1059–1063.10.1002/jhet.936
]Search in Google Scholar
[
Los R., M. Wesołowska-Trojanowska, A.M. Malm, M. Karpińska, J. Matysiak, A. Niewiadomy and U. Głaszcz. 2012. A new approach to the synthesis of 2-aryl-substituted benzimidazoles, quinazolines, and other related compounds and their antibacterial activity. Heteroatom Chemistry 23:265–275.10.1002/hc.21012
]Search in Google Scholar
[
Martin R.J. 1997. Modes of action of anthelmintic drugs. Vet. J. 154: 11–34.10.1016/S1090-0233(05)80005-X
]Search in Google Scholar
[
Navarrete-Vázquez G., M.e.M. Rojano-Vilchis, L. Yépez-Mulia, V. Meléndez, L. Gerena, A. Hernández-Campos, R. Castillo and F. Hernández-Luis. 2006. Synthesis and antiprotozoal activity of some 2-(trifluoromethyl)-1H-benzimidazole bioisosteres. Eur. J. Med. Chem. 41:135–141.10.1016/j.ejmech.2005.09.00116260067
]Search in Google Scholar
[
Padmavathi V., P. Thriveni, G. Sudhakar Reddy and D. Deepti. 2008. Synthesis and antimicrobial activity of novel sulfone-linked bis heterocycles. Eur. J. Med. Chem. 43: 917–924.10.1016/j.ejmech.2007.06.01117692433
]Search in Google Scholar
[
Pagano M.A., M. Andrzejewska, M. Ruzzene, S. Sarno, L. Cesaro, J. Bain, M. Elliott, F. Meggio, Z. Kazimierczuk and others. 2004. Optimization of protein kinase CK2 inhibitors derived from 4,5,6,7-tetrabromobenzimidazole. J. Med .Chem. 47: 6239–6247.
]Search in Google Scholar
[
Pedini M., G. Alunni Bistocchi, A. Ricci, L. Bastianini and E. Lepri. 1994. New heterocyclic derivatives of benzimidazole with germicidal activity-XII--Synthesis of N1-glycosyl-2-furyl benzimidazoles. Farmaco 49: 823–827.
]Search in Google Scholar
[
Sharma S., S. Gangal and A. Rauf. 2009. Convenient one-pot synthesis of novel 2-substituted benzimidazoles, tetrahydrobenzimidazoles and imidazoles and evaluation of their in vitro antibacterial and antifungal activities. Eur. J. Med. Chem. 44: 1751–1757.
]Search in Google Scholar
[
Shingalapur R.V., K.M. Hosamani and R.S. Keri. 2009. Synthesis and evaluation of in vitro anti-microbial and anti-tubercular activity of 2-styryl benzimidazoles. Eur. J. Med. Chem. 44: 4244–4248.10.1016/j.ejmech.2009.05.02119540630
]Search in Google Scholar
[
Tunçbilek M., T. Kiper and N. Altanlar. 2009. Synthesis and in vitro antimicrobial activity of some novel substituted benzimidazole derivatives having potent activity against MRSA. Eur. J. Med. Chem. 44: 1024–1033.10.1016/j.ejmech.2008.06.02618718694
]Search in Google Scholar
[
Vinodkumar R., S.D. Vaidya, B.V. Siva Kumar, U.N. Bhise, S.B. Bhirud and U.C. Mashelkar. 2008. Synthesis, anti-bacterial, anti-asthmatic and anti-diabetic activities of novel N-substituted- 2-(4-phenylethynyl-phenyl)-1H-benzimidazoles and N-substituted 2[4-(4,4-dimethyl-thioc hroman-6-yl-ethynyl)-phenyl)-1H-benzi- midazoles. Eur. J. Med. Chem. 43: 986–995.
]Search in Google Scholar
[
Zacny V.L., E. Gershburg, M.G. Davis, K.K. Biron and J.S. Pagano. 1999. Inhibition of Epstein-Barr virus replication by a benzimidazole L-riboside: novel antiviral mechanism of 5, 6-dichloro- 2-(isopropylamino)-1-beta-L-ribofuranosyl-1H-benzimidazole. J. Virol. 73: 7271–7277.
]Search in Google Scholar