A novel ligand, 1-(4-methoxybenzylidene)-4-methylthiosemicarbazone (MBT) derived from 4-methoxybenzaldehyde was synthesized and characterized by spectroscopic methods (IR, 1 H NMR, 13 C NMR), single crystal X-ray diffraction technique and physical means. MBT showed antibacterial activity in vitro with MICs of 64 μg/mL (a strain of Salmonella typhi (ATCC 6539)), 128 μg/mL ( Salmonella typhi ), 64 μg/mL ( Salmonella paratyphi A ), 128 μg/mL ( Salmonella paratyphi B ) and 64 μg/mL ( Salmonella typhimurium ) . The results showed that MBT demonstrated moderate in vitro antibacterial activity against a strain of Salmonella typhi (ATCC 6539), Salmonella paratyphi A , and Salmonella typhimurium , indicating its promise as a possible lead for the discovery of antibacterial drugs.
Fahlbusch, K.-G., Franz-Josef, H., Panten, J., Pickenhagen, W., Schatkowski, D., Kurt, B., Garbe, D. and Surburg, H. (2003) Flavors and Fragrances in Ullmann’s Encyclopedia of Industrial Chemistry. Wiley-VCH, Weinheim.
Parul, N., Subhangkar, N. and Mahato, A. (2012) Antimicrobial Activity of Different Thiosemicarbazone Compounds against Microbial Pathogens. International Research Journal of Pharmacy, 3, 350-363.
Abou-Mehla, K.S. and Faruk, H. (2008) Bimetallic Complexes of Schiff Base Bis-[4-Hydroxycoumarin-3-yl]-1N,5N-Thiocarbohydrazone as a Potentially Dibasic Pentadentate Ligand. Synthesis, Spectral and Antimicrobial Properties. Journal of the Iranian Chemical Society, 5, 122-134. https://doi.org/10.1007/BF03245825
Patil, S.A., Naik, V.H., Kulkarni, A.D. and Badami, P.S. (2010) DNA Cleavage, Antimicrobial, Spectroscopic and Fluorescence Studies of Co(II), Ni(II) and Cu(II) Complexes with SNO Donor Coumarin Schiff Bases. Spectrochimica Acta A, 75, 347-354. https://doi.org/10.1016/j.saa.2009.10.039
Teytz, Y., Ronen, D., Vansover, A., Stematsky, T. and Riggs, J.L. (1994) Inhibition of Human Immunodeficiency Virus by N-Methylisatin-Beta4’:4’-Diethylthiose-micarbazoneand N-Allylisatin-Beta4’:4’-Diallythiosemicarbazone. Antiviral Research, 24, 305-314.
Teytz, Y., Barko, N., Abramoff, M. and Ronen, D. (1994) Relationships between Structure and Antiretroviral Activity of Thiosemicarbazone Derivatives. Chemotherapy, 40, 195-200. https://doi.org/10.1159/000239192
Jones, D.H., Slack, R., Squires, S. and Wooldridge, K.R.H. (1965) Antiviral Chemotherapy.1. The Activity of Pyridine and Quinoline Derivatives against Neurovaccinia in Mice. Journal of Medicinal Chemistry, 8, 676-680. https://doi.org/10.1021/jm00329a026
Hall, I.H., Wong, O.T. and Chapman, J.M. (1995) Cytotoxicity of Imides-N-Alkyl Semicarbazones, Thiosemicarbazones, Acetylhydrazones and Related Derivatives. Anticancer Drugs, 6,147-153. https://doi.org/10.1097/00001813-199502000-00017
Tahmeena, K., Rumana, A., Seema, J. and Khan, A.R. (2015) Anticancer Potential of Metal Thiosemicarbazone Complexes: A Review. Der Chemica Sinica, 6, 1-11.
Liu, M., Lin, T. and Sartorelli, A.C. (1992) Synthesis and Antitumor Activity of Amino Derivatives of Pyridine-2-Carboxaldehyde Thiosemicarbazone. Journal of Medicinal Chemistry, 35, 3672-3677. https://doi.org/10.1021/jm00098a012
Mignot, A., Miocque, M., Binet, P., Rapin, J.R., Rinjard, P., Roux, M., Cals, M.J. and Ekindjian, J.C. (1980) Thiosemicarbazones D’Aldéhydes Aromatiques Antiinflammatoires: Pharmacologie, étude Pharmacocinétique Preliminaire, Action sur le Fibroblaste en Culture. European Journal of Medicinal Chemistry, 15, 33-40.
Bemstein, J., Yale, H.L., Losee, K., Holsing, M., Martins, J. and Lott, W.A. (1951) The Chemotherapy of Experimental Tuberculosis. III. The Synthesis of Thiosemicarbazones and Related Compounds. Journal of the American Chemical Society, 73, 906-912. https://doi.org/10.1021/ja01147a007
Klayman, D.L., Bartosevich, J.F., Mason, C.J. and Scovill, J.P. (1979) 2-Acetylpyri-Dinethiosemicarbazones, a New Class of Potential Antimalarial Agents. Journal of Medicinal Chemistry, 22, 855-883. https://doi.org/10.1021/jm00193a020
Klayman, D.L., Scovill, J.P., Bartosevich, J.F. and Mason, C.J. (1979) 2-Acetylpyri-Dinethiosemicarbazones, N4, N4-Disubstituted Derivatives as Potential Antimalarial Agents. Journal of Medicinal Chemistry, 22, 1367-1373. https://doi.org/10.1021/jm00197a017
Mbah, J.A., Ayimele, G.A., Eyonganyo, E.N. and Nfor, E.N. (2017) Synthesis, Molecular Structure and Antibacterial Activity of Benzylmethyl-4-Methyl-3-Thiosemi-Carbazone. International Journal of Organic Chemistry, 7, 83-90. https://doi.org/10.4236/ijoc.2017.72007
Gatsing, D., Mbah, J.A., Garba, I.H., Tane, P., Djemgou, P. and Nji-Nkah, B.F. (2006) An Antisalmonellal Agent from the Leaves of Glossocalyx brevipes Benth (Monimiaceae). Pakistan Journal of Biological Sciences, 9, 84-87. https://doi.org/10.3923/pjbs.2006.84.87
Gatsing, D. and Adoga, G.I. (2007) Antisalmonellal Activity and Phytochemical Screening of the Various Parts of Cassia Petersiana bolle (Caesalpiniaceae). Microbiology, 2, 876-880.
Cheesbrough, M. (1991) Medical Laboratory Manual for Tropical Countries: Microbiology. ELBS Edition, Cambridge, 196-205.
Nfor, E.N., Ahmad, H., Majoumo-Mbe, F., Njah, I.N., Offiong, E.O. and Bourne, S. (2013) Synthesis, Crystal Structure and Antifungal Activity of a Ni(II) Complex of a New Hydrazone Derived from Antihypertensive Drug Hydralazine Hydrochloride. Polyhedron, 63, 207-213. https://doi.org/10.1016/j.poly.2013.07.028
Mativandlela, S.P.N., Lall, N. and Meyer, J.J.M. (2006) Antibacterial, Antifungal and Antitubercular Activity of (the Roots of) Pelargonium reniforme (CURT) and Pelargonium sidoides (DC) (Geraniaceae) Root Extracts. South African Journal of Botany, 72, 232-237. https://doi.org/10.1016/j.sajb.2005.08.002
Kuete, V., Ngameni, B., Fotso, S.C.C., Kengap, T.R., Ngadjui, B.T., Meyer, J.J.M., et al. (2008) Antimicrobial Activity of the Crude Extracts and Compounds from Ficus chlamydocarpa and Ficus cordata (Moraceae). Journal of Ethnopharmacology, 120, 17-24. https://doi.org/10.1016/j.jep.2008.07.026
Majoumo-Mbe, F., Nde, D.T., Mukoko, I.N., Offiong, E.O. and Nfor, E.N. (2016) Synthesis, Crystal and Molecular Structure of Manganese (II) Complex of 2-Acetl-pyridine N (4) Ethylthiosemicarbazone. Communications in Inorganic Synthesis, 4, 5-11.
Kuete, V. (2010) Potential of Cameroonian Plants and Derived Products against Microbial Infections. Planta Medica, 76, 1-13. https://doi.org/10.1055/s-0030-1250027
Carbonelle, B., Denis, F., Marmonier, A., Pinon, G. and Vague, R. (1987) Bactériologie Médicale: Techniques Usuelles. SIMEP Edition, Paris, 228-282.