Copyright (c) 2018 AJC
This work is licensed under a Creative Commons Attribution 4.0 International License.
Antibacterial Screening of New Synthesis Schiff Base having Benzimidazole Moiety
Corresponding Author(s) : Muayed Ahmed Redayan
Asian Journal of Chemistry,
Vol. 30 No. 2 (2018): Vol 30 Issue 2
Abstract
A new series of benzimidazole containing Schiff base moiety has been synthesized. The reaction was achieved through cyclocondensation reaction of the substituted 1,2-phenylenediamines and amino acids (glycine, alanine and tyrosine) to gave substituted benzimidazole derivatives 1(a-f). Condensation of these compounds with a variety of aromatic aldehyde yielded the new benzimidazole substituted Schiff base. The chemical structures of the synthesized compounds were confirmed by FT-IR, 1H NMR and 13C NMR. Selected compounds were tested in vitro for their antibacterial activity by disc diffusion method against two types of Gram-positive bacteria namely (Staphylococcous aureus, Bacillus subtilis) and Gram-negative bacteria namely (Pseudomonas aeruginosa, Escherichia coli). The results displayed that most of the prepared compounds have a good antibacterial activity in compared with the standard antibiotic ampicillin and ciprofloxacin.
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G. Mariappan, R. Hazarika, F. Alam, R. Karki, U. Patangia and S. Nath, Arab. J. Chem., 8, 715 (2015); https://doi.org/10.1016/j.arabjc.2011.11.008.
M. Gaba, S. Singh and C. Mohan, Eur. J. Med. Chem., 76, 494 (2014); https://doi.org/10.1016/j.ejmech.2014.01.030.
A.O. El-Nezhawy, A.R. Biuomy, F.S. Hassan,A.K. Ismaiel and H.A. Omar, Bioorg. Med. Chem., 21, 1661 (2013); https://doi.org/10.1016/j.bmc.2013.01.070.
M. Gaba, D. Singh, S. Singh, V. Sharma and P. Gaba, Eur. J. Med. Chem., 45, 2245 (2010); https://doi.org/10.1016/j.ejmech.2010.01.067.
S. Rajasekaran, R. Gopalkrishna and C. Abhiskek, Int. J. Drug Develop. Res., 4, 303 (2012).
J.R. Kumar, L. Jawahar and D. Pathak, E-J. Chem., 3, 278 (2006).
A.K. Tewari and A. Mishra, Indian J. Chem., 45B, 489 (2006).
G. Vitale, P. Corona, M. Loriga,A. Carta, G. Paglietti, G. Giliberti, G. Sanna, P. Farci, M.E. Marongiu and P. La Colla, Eur. J. Med. Chem., 53, 83 (2012); https://doi.org/10.1016/j.ejmech.2012.03.038.
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M. Alp, H. Göker, R. Brun and S. Yildiz, Eur. J. Med. Chem., 44, 2002 (2009); https://doi.org/10.1016/j.ejmech.2008.10.003.
A. Husain, M. Rashid, M. Shaharyar, A.A. Siddiqui and R. Mishra, Eur. J. Med. Chem., 62, 785 (2013); https://doi.org/10.1016/j.ejmech.2012.07.011.
H.M. Refaat, Eur. J. Med. Chem., 45, 2949 (2010); https://doi.org/10.1016/j.ejmech.2010.03.022.
M. Rashid, A. Husain and R. Mishra, Eur. J. Med. Chem., 54, 855 (2012); https://doi.org/10.1016/j.ejmech.2012.04.027.
K. Gobis, H. Foks, K. Suchan, E. Augustynowicz-Kopec, A. Napiorkowska and K. Bojanowski, Bioorg. Med. Chem., 23, 2112 (2015); https://doi.org/10.1016/j.bmc.2015.03.008.
R.V. Shingalapur, K.M. Hosamani and R.S. Keri, Eur. J. Med. Chem., 44, 4244 (2009); https://doi.org/10.1016/j.ejmech.2009.05.021.
C.G. Neochoritis, T. Zarganes-Tzitzikas, C.A. Tsoleridis, J. StephanidouStephanatou, C.A. Kontogiorgis, D.J. Hadjipavlou-Litina and T. Cholipapadopoulou, Eur. J. Med. Chem., 46, 297 (2011); https://doi.org/10.1016/j.ejmech.2010.11.018.
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K.P. Barot, K.S. Manna and M.D. Ghate, J. Saudi Chem. Soc., 21, 535 (2017); https://doi.org/10.1016/j.jscs.2013.09.010.
V. Namani, B.B.K. Goud, Y.B. Kumari, R. Kumbham, K. Balakrishna and B. Bhima, Asian J. Chem., 27, 4575 (2015); https://doi.org/10.14233/ajchem.2015.19235.
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K. Parikh and D. Joshi, Med. Chem. Res., 22, 3688 (2013); https://doi.org/10.1007/s00044-012-0369-3.
R. Vinodkumar, S.D. Vaidya, B.V. Siva Kumar, U.N. Bhise, S.B. Bhirud and U.C. Mashelkar, Eur. J. Med. Chem., 43, 986 (2008); https://doi.org/10.1016/j.ejmech.2007.06.013.
J. Gowda, A.M. Khader, B. Kalluraya and S. Hidayathulla, Indian J. Chem., 50B, 1491 (2011).
A. Rao, A. Chimirri, E. De Clercq, A.M. Monforte, P. Monforte, C. Pannecouque and M. Zappalà, IL Farmaco, 57, 819 (2002); https://doi.org/10.1016/S0014-827X(02)01300-9.
M. Hranjec, K. Starcevic, S.K. Pavelic, P. Lucin, K. Pavelic and G.K. Zamola, Eur. J. Med. Chem., 46, 2274 (2011); https://doi.org/10.1016/j.ejmech.2011.03.008.
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G. Kumaravel and N. Raman, Mater. Sci. Eng. C, 70, 184 (2017); https://doi.org/10.1016/j.msec.2016.08.069.
B. Vishwanathan and B. Gurupadayya, J. Korean Chem. Soc., 58, 450 (2014); https://doi.org/10.5012/jkcs.2014.58.5.450.
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