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Copyright (c) 2014 R.A. Al-Salahi1, M.S. Marzouk1
This work is licensed under a Creative Commons Attribution 4.0 International License.
Some 2-Amino-benzo[de]isoquinolin-1,3-diones as Antimicrobial Agents
Corresponding Author(s) : R.A. Al-Salahi1
Asian Journal of Chemistry,
Vol. 26 No. 23 (2014)
Abstract
A new series of 2-amino-benzo[de]isoquinolin-1,3-diones was evaluated in vitro for their antimicrobial activity. The tested compounds were investigated against a variety of species of Gram negative bacteria (E. coli RCMB 010052 and Pseudomonas aeroginosa RCMB 010043) and Gram positive bacteria (Bacillis subtilis RCMB 010067 and Streptococcus pneumoniae RCMB 010010). Furthermore, they were screened against several types of fungi as Syncephalastrum racemosum (RCMB 05922), Aspergillus fumigatus (RCMB 02568), Candida albicans (RCMB 05036) and Geotricum candidum (RCMB 05097). The minimum inhibitory concentration (MIC) of the tested molecules was determined using broth double dilution method (Serially diluted technique) in proper nutrient. The findings revealed that compounds 1, 3, 7, 10, 12, 13, 14 and 16 have shown as potential antimicrobial agents and could be useful as corner stones for further development to design more potent antimicrobial agents.
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- T. Saga and K. Yamaguchi, Jap. Med. Assoc. J., 52, 103 (2009).
- Y. Xu, B. Qu, X. Qian and Y. Li, Bioorg. Med. Chem. Lett., 15, 1139 (2005).
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- M.F. Brana, J.M. Castellano, M. Moran, M.J. Perez de Vega, C.A. Romerdahl, X.D. Qian, P. Bousquet, F. Emling, K. Schlick and G. Keilhauer, Anticancer Drug Des., 8, 257 (1993).
- A. Wu, J. Liu, S. Qin and P. Mei, Monatsh. Chem., 141, 95 (2010).
- A. Mukherjee, S. Dutta, M. Shanmugavel, D.M. Mondhe, P.R. Sharma, S.K. Singh, A.K. Saxena and U. Sanyal, J. Exp. Clin. Cancer Res., 29, 175 (2010).
- E. Lacivita, M. Leopoldo, A.C. Masotti, C. Inglese, F. Berardi, R. Perrone, S. Ganguly, M. Jafurulla and A. Chattopadhyay, J. Med. Chem., 52, 7892 (2009).
- R. Al-Salahi, I. Alswaidan, M. Al-Omar and M. Marzouk, Life Sci. J., 10, 2018 (2013).
- R. Al-Salahi, M. Marzouk, G. Awad, M. Al-Omar and E. Ezzeldin, J. Pharm. Pharmacol., 65, 790 (2013).
- A.C. Scott, in eds.: J.G. Collee, J.P. Duguid, A.G. Fraser and B.P. Marmion, Laboratory Control of Antimicrobial Therapy. In: Practical Medical Microbiology, Churchill Livingstone, Edinburgh, edn 13, pp. 161-181 (1989).
- C. Perez, M. Pauli and P. Bazerque, Acta Biol. Med. Exp., 15, 113 (1999).
- R. Al-Salahi and M. Marzouk, Asian J. Chem., 26, 2166 (2014).
- R. Al-Salahi and D. Geffken, Heterocycles, 81, 1843 (2010).
- R. Al-Salahi and D. Geffken, Molecules, 15, 7016 (2010).
- R. Al-Salahi and D. Geffken, Synth. Commun., 41, 3512 (2011).
References
T. Saga and K. Yamaguchi, Jap. Med. Assoc. J., 52, 103 (2009).
Y. Xu, B. Qu, X. Qian and Y. Li, Bioorg. Med. Chem. Lett., 15, 1139 (2005).
A. Mukherjee, S. Hazra, S. Dutta, S. Muthiah, D.M. Mondhe, P.R. Sharma, S.K. Singh, A.K. Saxena, G.N. Qazi and U. Sanyal, Invest. New Drugs, 29, 434 (2011).
M.F. Brana, J.M. Castellano, M. Moran, M.J. Perez de Vega, C.A. Romerdahl, X.D. Qian, P. Bousquet, F. Emling, K. Schlick and G. Keilhauer, Anticancer Drug Des., 8, 257 (1993).
A. Wu, J. Liu, S. Qin and P. Mei, Monatsh. Chem., 141, 95 (2010).
A. Mukherjee, S. Dutta, M. Shanmugavel, D.M. Mondhe, P.R. Sharma, S.K. Singh, A.K. Saxena and U. Sanyal, J. Exp. Clin. Cancer Res., 29, 175 (2010).
E. Lacivita, M. Leopoldo, A.C. Masotti, C. Inglese, F. Berardi, R. Perrone, S. Ganguly, M. Jafurulla and A. Chattopadhyay, J. Med. Chem., 52, 7892 (2009).
R. Al-Salahi, I. Alswaidan, M. Al-Omar and M. Marzouk, Life Sci. J., 10, 2018 (2013).
R. Al-Salahi, M. Marzouk, G. Awad, M. Al-Omar and E. Ezzeldin, J. Pharm. Pharmacol., 65, 790 (2013).
A.C. Scott, in eds.: J.G. Collee, J.P. Duguid, A.G. Fraser and B.P. Marmion, Laboratory Control of Antimicrobial Therapy. In: Practical Medical Microbiology, Churchill Livingstone, Edinburgh, edn 13, pp. 161-181 (1989).
C. Perez, M. Pauli and P. Bazerque, Acta Biol. Med. Exp., 15, 113 (1999).
R. Al-Salahi and M. Marzouk, Asian J. Chem., 26, 2166 (2014).
R. Al-Salahi and D. Geffken, Heterocycles, 81, 1843 (2010).
R. Al-Salahi and D. Geffken, Molecules, 15, 7016 (2010).
R. Al-Salahi and D. Geffken, Synth. Commun., 41, 3512 (2011).