Copyright (c) 2015 AJC
This work is licensed under a Creative Commons Attribution 4.0 International License.
Design, Synthesis and Biological Evaluation of Benzimidazolyl and Benzothiazolyl Picolinamide Derivatives as Antimicrobial Agents
Corresponding Author(s) : B. Bharath Kumar Goud
Asian Journal of Chemistry,
Vol. 27 No. 12 (2015): Vol 27 Issue 12
Abstract
A series of benzothiazolyl amides and benzimidazolyl amides (6a-f) has been synthesized from the coupling reaction of substituted picolinic acid with benzothiazole and benzimidazoles, respectively. The newly synthesized compounds were evaluated for their efficacy as antimicrobial agents against various Gram-positive and Gram-negative strains of bacteria and fungal strains. Amongst these compounds 6f was found to be the most potent against Bacillus subtilis and Candida albicans. Moreover, other compounds also found to be potential antibacterial agents in comparison to the standard drugs.
Keywords
Download Citation
Endnote/Zotero/Mendeley (RIS)BibTeX
- H. Bujdáková and M. Múčková, Int. J. Antimicrob. Agents, 4, 303 (1994); doi:10.1016/0924-8579(94)90030-2.
- A. Latrofa, M. Franco, A. Lopedota, A. Rosato, D. Carone and C. Vitali, IL Farmaco, 60, 291 (2005); doi:10.1016/j.farmac.2005.01.010.
- V.P. Devmurari, M.B. Goyani, R.R. Nandanwar and S. Pandey, Int. J. Chem. Tech. Res., 2, 681 (2010).
- C.G. Mortimer, G. Wells, J.-P. Crochard, E.L. Stone, T.D. Bradshaw, M.F.G. Stevens and A.D. Westwell, J. Med. Chem., 49, 179 (2006); doi:10.1021/jm050942k.
- B. Soni, M.S. Ranawat, R. Sharma, A. Bhandari and S. Sharma, Eur. J. Med. Chem., 45, 2938 (2010); doi:10.1016/j.ejmech.2010.03.019.
- B. Soni, M.S. Ranawat, R. Sharma, A. Bhandari and S. Sharma, Eur. J. Med. Chem., 45, 2938 (2010); doi:10.1016/j.ejmech.2010.03.019.
- F.W. Bell, A.S. Cantrell, M. Hoegberg, S.R. Jaskunas, N.G. Johansson, C.L. Jordan, M.D. Kinnick, P. Lind and J.M. Morin, J. Med. Chem., 38, 4929 (1995); doi:10.1021/jm00025a010.
- R.L. Mital and S.K. Jain, J. Chem. Soc. C, 2148 (1969); doi:10.1039/J39690002148.
- W.C. Patt, H.W. Hamilton, M.D. Taylor, M.J. Ryan, D.G. Taylor, C.J.C. Connolly, A.M. Doherty, S.R. Klutchko and I. Sircar, J. Med. Chem., 35, 2562 (1992); doi:10.1021/jm00092a006.
- M.T. Migawa, J.-L. Girardet, J.A. Walker, G.W. Koszalka, S.D. Chamberlain, J.C. Drach and L.B. Townsend, J. Med. Chem., 41, 1242 (1998); doi:10.1021/jm970545c.
- B.S. Holla, K.V. Malini, B.S. Rao, B.K. Sarojini and N.S. Kumari, Eur. J. Med. Chem., 38, 313 (2003); doi:10.1016/S0223-5234(02)01447-2.
- P.S. Yadav and G.P. Senthilkumar, Int. J. Pharm. Sci. Drug Res., 3, 1 (2011).
- P. Meier, S. Legraverant, S. Müller and J. Schaub, Synthesis, 551 (2003); doi:10.1055/s-2003-37663.
- National Committee for Clinical Laboratory Standards (NCCLS), Standard Methods for Dilution Antimicrobial Susceptibility Tests for Bacteria, which Grows Aerobically; Approved standard—5th edn, Approved Standard NCCLS Document M7-A5. NCCLS: Wayne, PA (2003).
- A. Kamal, M.N.A. Khan, K.S. Reddy, Y.V.V. Srikanth and B. Sridhar, Chem. Biol. Drug Des., 71, 78 (2008); doi:10.1111/j.1747-0285.2007.00609.x.
References
H. Bujdáková and M. Múčková, Int. J. Antimicrob. Agents, 4, 303 (1994); doi:10.1016/0924-8579(94)90030-2.
A. Latrofa, M. Franco, A. Lopedota, A. Rosato, D. Carone and C. Vitali, IL Farmaco, 60, 291 (2005); doi:10.1016/j.farmac.2005.01.010.
V.P. Devmurari, M.B. Goyani, R.R. Nandanwar and S. Pandey, Int. J. Chem. Tech. Res., 2, 681 (2010).
C.G. Mortimer, G. Wells, J.-P. Crochard, E.L. Stone, T.D. Bradshaw, M.F.G. Stevens and A.D. Westwell, J. Med. Chem., 49, 179 (2006); doi:10.1021/jm050942k.
B. Soni, M.S. Ranawat, R. Sharma, A. Bhandari and S. Sharma, Eur. J. Med. Chem., 45, 2938 (2010); doi:10.1016/j.ejmech.2010.03.019.
B. Soni, M.S. Ranawat, R. Sharma, A. Bhandari and S. Sharma, Eur. J. Med. Chem., 45, 2938 (2010); doi:10.1016/j.ejmech.2010.03.019.
F.W. Bell, A.S. Cantrell, M. Hoegberg, S.R. Jaskunas, N.G. Johansson, C.L. Jordan, M.D. Kinnick, P. Lind and J.M. Morin, J. Med. Chem., 38, 4929 (1995); doi:10.1021/jm00025a010.
R.L. Mital and S.K. Jain, J. Chem. Soc. C, 2148 (1969); doi:10.1039/J39690002148.
W.C. Patt, H.W. Hamilton, M.D. Taylor, M.J. Ryan, D.G. Taylor, C.J.C. Connolly, A.M. Doherty, S.R. Klutchko and I. Sircar, J. Med. Chem., 35, 2562 (1992); doi:10.1021/jm00092a006.
M.T. Migawa, J.-L. Girardet, J.A. Walker, G.W. Koszalka, S.D. Chamberlain, J.C. Drach and L.B. Townsend, J. Med. Chem., 41, 1242 (1998); doi:10.1021/jm970545c.
B.S. Holla, K.V. Malini, B.S. Rao, B.K. Sarojini and N.S. Kumari, Eur. J. Med. Chem., 38, 313 (2003); doi:10.1016/S0223-5234(02)01447-2.
P.S. Yadav and G.P. Senthilkumar, Int. J. Pharm. Sci. Drug Res., 3, 1 (2011).
P. Meier, S. Legraverant, S. Müller and J. Schaub, Synthesis, 551 (2003); doi:10.1055/s-2003-37663.
National Committee for Clinical Laboratory Standards (NCCLS), Standard Methods for Dilution Antimicrobial Susceptibility Tests for Bacteria, which Grows Aerobically; Approved standard—5th edn, Approved Standard NCCLS Document M7-A5. NCCLS: Wayne, PA (2003).
A. Kamal, M.N.A. Khan, K.S. Reddy, Y.V.V. Srikanth and B. Sridhar, Chem. Biol. Drug Des., 71, 78 (2008); doi:10.1111/j.1747-0285.2007.00609.x.