Antimicrobial activity of Schiff Base of 2-Amino 5-Nitrothiazole and its Copper complex
Abstract
In an attempt to find out a new class of antimicrobial agents new schiff base ligand of 2-amino 5-nitro thiazole and its copper complex were prepared. The Microwave assisted synthesis was carried out by condensation of 2-amino 5-nitro thiazole and substituted salicyldehyde. The newly synthesized schiff base ligand and its copper complex were tested against representatives of gram-positive (Staphylococcus aureus, Bacillus subtilis) and gram- negative bacteria (E. coli, Pseudomonas putida) and fungi (Candida albicans, Aspergillus niger) by disc diffusion method.
References
A.B.P. Lever (1984); Inorganic electronic spectroscopy Elsevier, Amsterdam.
Ahmed Hassen Shntaif, Zahraa M. Rashid, (2016); The Synthesis of Schiff bases under microwave Irradiation: Review, Journal of Chemical and Pharmaceutical Science; 9(3); 1066-1068
Ahmed R. Ali, Eman R. El-Bendary, Mariam A. Ghaly, Ihsan A. Shehata (2014); Synthesis, in vitro anticancer evaluation and in silico studies of novel imidazo[2,1-b] thiazole derivatives bearing pyrazole moieties; European Journal of Medicinal Chemistry; 75; 492-500.
Amit S. Lunkad, Sachin N. Kothawade, Krishna K. Darkunde, Bhanu Priya, Ujwala R. Bagmar and Dipali S. Bhandari (2013); Synthesis and Screening Antihelminitic Activity of Some Thiazole Derivatives; Int. J. Chem. Sci.; 11(2); 1146-1152.
B.C.J. Bayer (1962); An introduction to ligand field. McGraw Hill, New York.
Balaji P. N., N. Chanukya, A. Keerthi, Mohana. C, K. Hima Bindu and S. Priyanka (2014); In vitro anthelmintic and antimicrobial activity of synthesized fluoro & nitro substituted N-[(Z)-phenylmethylidene]-1,3-benzothiazol-2- amine and its derivatives; Pelagia Research Library der Chemica Sinica; 5(1); 110-114.
Chohan ZH, Scozzafava A, Supuran CT (2002); Unsymmetrical 1,1-disubstituted ferrocenes: synthesis of Co(II), Cu(II), Ni(II) and Zn(II) chelates of ferrocenyl-1-thiadiazolo-1- tetrazole-1-thiadiazolo-1-triazole and -1-tetrazolo-1-triazole with antimicrobial properties; J Enzym Inhib Med Chem; 17(4); 261–266.
Dash B, Praharaj S and Mohapatra PK (1981); Thiazolidone derivatives; J Indian Chem Soc.; 58(12); 1184-1186.
Faiz Arshad, Nadeem Siddiqui, Ahmed Elkerdasy, Abdulmohsen H. Al Rohaimi and Suroor A. Khan (2014); Anticonvulsant and Neurotoxicity Evaluation of Some Newly Synthesized Thiazolyl Coumarin Derivative; American Journal of Pharmacology and Toxicology; 9(2); 132-138
Firas A. Hassan (2012); Synthesis, Characterization, Anti-inflammatory, and Antioxidant Activities of Some New Thiazole Derivatives, International Journal of Applied Science and Technology; 2(7); 180-187
Funda Tay, Cell Erkan, Nalan Yilmaz Sariozlu Emel, Seref Demirayak (2017); Synthesis, antimicrobial and anticancer activities of some naphthylthiazolylamine derivatives; Biomedical Research; 28(6); 2696-2703.
Gadada Naganagowda, Reinout Meijboom, and Amorn Petsom (2014); Synthesis and Antimicrobial Activity of New Schiff Base Compounds Containing 2-Hydroxy-4-pentadecylbenzaldehyde Moiety, Hindawi Publishing Corporation Advances in Chemistry; Article ID 921857, 9 pages
Hassan UM, Chohan ZH, Supuran CT (2002); Antibacterial Zn(II) compounds of Schiff base derived from some benzothiazoles; Main Group Met Chem; 25(5); 291-296.
J. Parekh, P. Inamdhar, R. Nair, S. Baluja, S. Chandra (2005); Synthesis and antibacterial activity of some Schiff bases derived from 4-aminobenzoic acid; J. Serb. Chem. Soc; 70(10); 1155–1161.
Khalid Mohammed Khan, Nida Ambreen, Aneela Karim, Sumayya Saied, Afroze Amyn, Aqeel Ahmed, and Shahnaz Perveen (2012); Schiff Bases of Thiazole as Antibacterial and Antifungal Agents; Journal of Pharmacy Research; 5(1); 651-656.
Metzger JV (1979); The Chemistry of Heterocyclic Compounds, A Series of Monographs, Thiazole and Its Derivatives, Wiley, Chichester.
Nour E. A. Abdel-Sattar, Abeer M. El-Naggar, and M. S. A. Abdel-Mottaleb (2017); Novel Thiazole Derivatives of Medicinal Potential: Synthesis and Modeling, Hindawi Journal of Chemistry, Article ID 4102796; 11 pages
Nuray Ulusoy Guzeldemirci, Berin Karaman, Ömer Kucukbasmaci (2017); Antibacterial, Antitubercular and Antiviral Activity Evaluations of Some Arylidenehydrazide Derivatives Bearing Imidazo[2,1-b] thiazole Moiety, Turk J Pharm Sci; 14(2); 157-163.
R. Pal, V. Kumar, A.K. Gupta, V. Hassan UM, Chohan ZH, Supuran CT. (2002) ; Antibacterial Zn(II) compounds of Schiff base derived from some benzothiazoles. Main Group Met Chem; 25(5); 291-296.
S. K. Sengupta, O. P. Pandey, B. K. Srivastava, V. K. Sharma (1998); Synthesis, structural and biochemical aspects of titanocene and zirconocene chelates of acetylferrocenyl thiosemicarbazones; Transition Met. Chem. 23(4); 349-353.
S. Muralikrishna, P. Raveendrareddy, L. K. Ravindranath, S. Harikrishna and P. Jagadeeswara Rao (2013); Synthesis Characterization and antitumor activity of thiazole derivatives containing indole moiety bearing-tetrazole; Der Pharma Chemica; 5(6); 87-93
Sobhi M. Gomha, Nabila A. Kheder, Mohamad R. Abdelaziz, Yahia N. Mabkhot, Ahmad M. Alhajoj, Gomha et al (2017); A facile synthesis and anticancer activity of some novel thiazoles carrying 1,3,4-thiadiazole moiety; Chemistry Central Journal; 11; 25.
Troutman H D and Long L M (1948); The synthesis of 2,3-disubstituted-4-thiazolidones; J Am Chem Soc.; 70(10); 3436-3439.
Wen-Xi Cai, Ai-Lin Liu, Zheng-Ming Li, Wei-Li Dong, Xing-Hai Liu and Na-Bo Sun (2016); Synthesis and Anticancer Activity of Novel Thiazole-5-Carboxamide Derivatives; Applied Sciences; 6(8); 1-10
Y. Vaghasia, R. Nair, M. Soni, S. Baluja, S. Chandra (2004); Synthesis, structural determination and antibacterial activity of compounds derived from vanillin and 4-aminoantipyrine; J. Serb. Chem. Soc.; 69 (12); 991-998

