Antibacterial Activities of New Schiff Bases and Intermediate Silyl Compounds Synthesized from 5-Substituted-1,10-phenanthroline- 2,9-dialdehyde
- 1 Department of Chemistry, Tennessee State University, Nashville, USA
- 2 Department of Chemistry, Tennessee State University, Nashville, USA
- 3 Department of Agriculture, Tennessee State University, Nashville, USA
- 4 Faculty of Science, Universiti Brunei Darussalam, Bandar Seri Begawan, Brunei
Abstract
Schiff bases are known to possess anticancer, antibacterial, antifungal, antitubercular, anti-inflammatory, antimicrobial and antimalarial properties. In this paper antibacterial studies against variety of plants and human pathogenic bacteria with eight newly synthesized Schiff bases and several intermediate silyl compounds have been reported. The antibacterial activities of the synthesized compounds were primarily determined by paper disc diffusion method. The minimum inhibitory concentration (MIC) of each compound was also determined by tube dilution process. Seven different human pathogenic bacteria and eighteen different plant pathogenic bacteria were used for the antibacterial activity studies. While all synthesized compounds have shown significant antibacterial activity, one intermediate silyl compound has shown remarkably high antibacterial property. 5-substituted derivatives have shown relatively higher activity than non-substituted compounds. Polar substituent which increases hydrophilicity may have a positive impact on the antibacterial property.
- Bell, S.C., Conklin, G.L. and Childress, S.J. (1963) The Separation of Ketimine Isomers. Journal of the American Chemical Society, 85, 2868-2869. http://dx.doi.org/10.1021/ja00901a057
- Khan, S.A., Siddiqui, A.A. and Bhatt, S. (2002) Analgesic Activity of Isatin Derivatives. Asian Journal of Chemistry, 14, 1117-1118.
- Capdeville, R., Buchdunger, E., Zinnermann, J. and Matter, A. (2002) Glivec (ST1571, Imatnib, a Rationally Developed, Targeted Anticancer Drug. Nature Reviews Drug Discovery, 1, 493-502. http://dx.doi.org/10.1038/nrd839
- Raman, N., Kulandaisamy, A., Shunmugasundaram, A. and Jeyasubramanian, K. (2001) Synthesis, Spectral, Redox and Antimicrobial Activities of Schiff Base Complexes Derived from 1-Phenyl-2,3-dimethyl-4-aminopyrazol-5-one and Acetoacetanilide. Transition Metal Chemistry, 26, 131-135. http://dx.doi.org/10.1023/A:1007100815918
- Shivarama, H.B., Sooryanarayana, R.B., Shridhara, K. and Akber, A.P.M. (2000) Studies on arylfuran Derivatives: Part XI. Synthesis, Characterization and Biological Studies on Some Mannich Bases Carrying 2,4-Dichlorophenylfurfural Moiety. Il Farmaco, 54, 338-344. http://dx.doi.org/10.1016/S0014-827X(00)00033-1
- Chaha, V.K., Ranwa, N.S. and Dadheech, P.K. (1998) Synthesis and Screening of Biological Activity of Triazolothiadiazines and Triazolothiadiazoles. Journal of Phytological Research, 11, 201-202.
- Sahu, R., Thakur, D.S. and Kashyap, P. (2012) Schiff Base: An Overview of Its Medicinal Chemistry Potential of New Drug Molecules. International Journal of Pharmaceutical Sciences and Nanotechnology, 5, 1757-1764.
- Mancin, F., Scrimin, P., Tecillab, P. and Tonellatoa, U. (2005) Artificial Metallonucleases. Chemical Communications, 2540-2548. http://dx.doi.org/10.1039/b418164f
- Cowan, A.J. (2001) Chemical Nucleases. Current Opinion in Chemical Biology, 5, 634-642.
- Goswami, K.T., Gadadhar, S., Karande, A.A. and Chakravarty, R.A. (2013) Photocytotoxic Ferrocene-Appended (L-Tyrosine)Copper(II) Complexes of Phenanthroline Bases. Polyhedron, 52, 1287-1298. http://dx.doi.org/10.1016/j.poly.2012.06.018
- Wheate, N.J., Taleb, R.I., Krause-Heuer, A.M., Cook, R.L., Wang, S., Higgins, V.J. and Aldrich-Wright, J.R. (2007) Novel Platinum(II)-Based Anticancer Complexes and Molecular Hosts as Their Drug Delivery Vehicles. Dalton Transactions, 43, 5055-5064.
- Klayman, D.L., Bartosevich, J.F., Griffin, T.S., Mason, C.J. and Scovill, J.P. (1979) 2-Acetylpyridine Thiosemicarbazones. 1. A New Class of Potential Antimalarial Agents. Journal of Medicinal Chemistry, 22, 855-862.http://dx.doi.org/10.1021/jm00193a020