Abstract: Synthesis and biological evaluation of (E)-5-(substituted benzylidene)-2-((4-(morpholine-4-carbonyl) thaiazol-2-yl) amino) thiazol-4(5H)-one and their derivatives (6a-j) were synthesized and their structure was established with the facility of spectroscopic techniques such as FTIR, 13C NMR, 1H NMR, Mass, etc. In-vitro antibacterial, antifungal, and antioxidant activities of the synthesized compounds 6a-j have been evaluated by using ampicillin, Nystatin, and Ascorbic acid as the reference standards. Compounds 6d, 6f, 6h and 6i have revealed comparable antibacterial activity by displaying similar MIC values as the reference standard used. Although 6i bearing strongly electron withdrawing substituent's showed prominent antioxidant activities compared with remaining derivatives compared to the reference standard. The compound 6i exerts multi-target inhibitory action against different microbial.
Keywords: Thiazole, Thiazolidinone; Antioxidant; Antimicrobial
[1]. N. Sahiba, A. Sethiya, J. Soni, A. K. Agarwal, S. Agarwal, Saturated Five Membered Thiazolidines And Their Derivatives: From Synthesis To Biological Applications. Topics Curr Chem. 2020, 378-34.
[2]. S. K. Manjal, R. Kaur, R. Bhatia, K. Kumar, V. Singh, R. Shankar, R. Kaur, R. K. Rawal, Synthetic And Medicinal Perspective Of Thiazolidinone: A Review. Bioorg. Chem. 2017, 75, 406-423.
[3]. Blaser, M. J. Antibiotic Use And Its Consequi.Uences For The Normal Microbiome. Science, 2016, 352, 544-545.
[4]. Ahpsr.Who.Int/Publications/I/Item/Global-Action-Pan-On-Antimicrobial-Resistance.
[5]. Falzon, D.; Schunemann, H. J.; Harausz, E.; Gonzalez-Angulo, L.; Lienhardt, C.; Jaramillo, E.; Weyer, K. World Health Organization Treatment Guidelines For Drug-Resistant Tuberculosis, 2016 Update, Eur. Respir. J. 2017, 49, 1602308.