Main Article Content
Abstract
A new series of 4-((5-(2-chlorophenyl)-1,3,4-oxadiazol-2-yl)methoxy)-N-(benzylidene derivatives)benzenamine (5a-k) have been synthesized and were screened for their in vitro antibacterial activity against Gram-positive bacteria (Pseudomonas aeruginosa, Streptococcus pyogenes), Gram-negative bacteria (Escherichia coli, Staphylococcus aureus) and antifungal activity (Candida albicans, Aspergillus niger, Aspergillus clavatus). Synthesized compounds were characterized by IR, mass (MS), 1H NMR and 13C NMR spectra. The synthesized compounds 5b, 5c, 5g and 5i showed potency in terms of antimicrobial activity against tested microorganisms.
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References
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References
S. Bala, S. Kamboj, A. Kajal, V. Saini and D. Prasad, 1,3,4-Oxadiazole Derivatives: Synthesis, Characterization, Antimicrobial Potential and Computational Studies, BioMed. Res. Int., 2014, 172791 (2014); https://doi.org/10.1155/2014/172791
P. Pitasse-Santos, V. Sueth-Santiago and M.E.F. Lima, 1,2,4- and 1,3,4-Oxadiazoles as Scaffolds in the Development of Antiparasitic Agents, J. Braz. Chem. Soc., 29, 435 (2018); https://doi.org/10.21577/0103-5053.20170208
A.O. Maslat, M. Abussaud, H. Tashtoush and M. Al-Talib, Synthesis, Antibacterial, Antifungal and Genotoxic Activity of bis-1,3,4-Oxadia-zole Derivatives, Pol. J. Pharmacol., 54, 55 (2002).
B.M. Sahoo, B.V. Ravi Kumar and K.B. Prasanna, Synthesis, Charac-terization and Biological Evaluation of Novel Oxadiazole Derivatives, Int. J. Pharm. Sci. Res., 2, 50 (2011).
D. Pal, D.R. Pany, B. Mohanty and A.K. Nayak, Evaluation of Spinacia oleracea L. Leaves Mucilage as an Innovative Suspending Agent, J. Adv. Pharm. Technol. Res., 1, 338 (2010); https://doi.org/10.4103/0110-5558.72430
A. Singh, S. Bose, U. Singh, S. Jana, R. Shukla, V. Singh and M. Lohani, Synthesis and Biological Activity of Some New Thiadiazole Derivative, Trends Pharm. Res., 2, 133 (2009).
R. Chawla, A. Arora, M. Parameswaran, P. Chan, D. Sharma, S. Michael and T. Ravi, Synthesis of Novel 1,3,4-oxadiazole Derivatives as Potential Antimicrobial Agents, Acta Pol. Pharm., 67, 247 (2010).
C.B. Chapleo, P.L. Myers, A.C.B. Smith, I.F. Tulloch and D.S. Walter, Substituted 1,3,4-Thiadiazoles with Anticonvulsant Activity. 3. Guanidines, J. Med. Chem., 30, 951 (1987); https://doi.org/10.1021/jm00388a038
Z. Chen, W. Xu, K. Liu, S. Yang, H. Fan, P.S. Bhadury, D.-Y. Huang and Y. Zhang, Synthesis and Antiviral Activity of 5-(4-Chlorophenyl)-1,3,4-Thiadiazole Sulfonamides, Molecules, 15, 9046 (2010); https://doi.org/10.3390/molecules15129046
D. Kumar, N.M. Kumar, K. Chang and K. Shah, Synthesis and Anti-cancer Activity of 5-(3-Indolyl)-1,3,4-thiadiazoles, Eur. J. Med. Chem., 45, 4664 (2010); https://doi.org/10.1016/j.ejmech.2010.07.023
D. Pal, D.D. Pandey, R. Tripathi and P. Mishra, J. Adv. Pharm. Technol. Res., 5, 196 (2014); https://doi.org/10.4103/2231-4040.143040
https://www.24chemicalresearch.com/reports/5852/nesapidil-2018-350
https://www.reportsnreports.com/reports/640722-nesapidil-global-market-and-forecast-research.html.
K. Kapadiya, Y. Jadeja, A. Banik and R. Khunt, in silico and in vitro Studies of Fluorinated Chroman-2-Carboxilic Acid Derivatives as an Anti-Tubercular Agent, Folia Med. (Plovdiv), 61, 95 (2019); https://doi.org/10.2478/folmed-2018-0034
K. Kapadiya and R. Khunt, Discovery of Hybrid Purine-quinoline Molecules and their Cytotoxic Evaluation, Lett. Drug Des. Discov., 16, 21 (2019); https://doi.org/10.2174/1570180815666180419151742
K. Kapadiya, Y. Jadeja and R. Khunt, Synthesis of Purine-based Triazoles by Copper (I)-Catalyzed Huisgen Azide-Alkyne Cycloaddition Reaction, J. Heterocycl. Chem., 55, 199 (2018); https://doi.org/10.1002/jhet.3025
M. Balouiri, M. Sadiki and S.K. Ibnsouda, Methods for in vitro Evaluating Antimicrobial Activity: A Review, J. Pharm. Anal., 6, 71 (2016); https://doi.org/10.1016/j.jpha.2015.11.005
I. Ali, P. Sharma, K.A. Suri, N.K. Satti, P. Dutt, F. Afrin and I.A. Khan, in vitro Antifungal Activities of Amphotericin B in Combination with Acteoside, A Phenylethanoid Glycoside from Colebrookea oppositifolia, J. Med. Microbiol., 60, 1326 (2011); https://doi.org/10.1099/jmm.0.031906-0