In-silico molecular docking study of some n-substituted thiazoles derivatives as FabH inhibitors

Shivkant Sharma *, Manish Devgun, Karan Wadhwa and Sahil Banwala

Institute of Pharmaceutical Sciences, Kurukshetra University, Kurukshetra, Haryana, 136119, India.
 
Research Article
World Journal of Advanced Research and Reviews, 2020, 08(02), 043-055
Article DOI: 10.30574/wjarr.2020.8.2.0387
 
Publication history: 
Received on 19 October 2020; revised on 27 October 2020; accepted on 02 November 2020
 
Abstract: 
Heterocyclic compounds with thiazole moiety are one of the most promising compounds in the medicinal chemistry possessing numerous therapeutic activities. The present was designed to study the high throughput in silico screening of 10 designed 2-phenyl-amino thiazole derivatives as a potent FABH inhibitor in Molegro virtual docker software (Version 6.0) using 3iL9 as PDB. The docking results showed mol dock score of -90.94 with four hydrogen bonding for the standard drugs griseofulvin, while on the other hand, N-substituted thiazole derivatives S2, S5, S6, S7, S8, and S9 exhibited excellent mol dock score, ranged from -102.612 to -144.236, hydrogen bonding (4-10), and docking score ranged from -104.873 to -143.593. Similarly, another in silico study was done using online PASS software and the compounds S1, S2, S5, S6, S7, S8, and S9 have Pa ranged between 0.310 to 0.411 and showed good antibacterial activity whereas, compounds having Pa ranged between 0.216 to 0.334 demonstrated potent antifungal activity when compared to standard drugs. Thus, the present study affirmed the significant antimicrobial potential of some designed N-substituted thiazole derivatives based on their mol dock values and other parameters when studies in silico and the obtained results will provide data support and offer perspectives in future researches to develop potent antimicrobial agents from these N-substituted thiazole derivatives.
 
Keywords: 
Antimicrobial; Antifungal; Thiazole; Molecular Docking; FabH Inhibitors
 
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