Synthesis, In-Silico and Biological Studies of thiazolyl-2h-chromen-2-one Derivatives as Potent Antitubercular Agents

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Author(s): Bhagwat S. Jadhav, Ramesh S. Yamgar*, Rajesh S. Kenny, Suraj N. Mali, Hemchandra K. Chaudhari, Mustapha C. Mandewale.

Journal Name: Current Computer-Aided Drug Design

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Background: A series of new six thiazolyl-2-amine based Schiff base derivatives (4a-4f) were synthesized by a sequential multistep reactions starting with Salicylaldehyde.

Objective: All the Schiff base derivatives were screened in-vitro for their antibacterial activity against Mycobacterium tuberculosis (H37RV strain) ATCC No-27294. The synthesized compounds were characterized by FTIR, 1H-NMR, 13C-NMR and Mass spectrometry.

Results: Among the compounds tested, 4c and 4f exhibited potent antitubercular activity against M. Tuberculosis at MIC 6.25 µg/mL.

Conclusion: We extended our study to explore the inhibition mechanism by conducting molecular docking analysis by using Schrodinger’s molecular modeling software. All the newly synthesized compounds were found to be in-silico AMES test non-toxic and non-carcinogens. The good Qikprop’s Absorption, Distribution, Metabolism and Excretion (ADMET) would definitely be help the researchers in order to make more potent Anti-TB agents.

Keywords: Thiazole, Coumarin, Schiff bases, Heterocyclic, Tuberculosis, Molecular docking

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Article Details

(E-pub Ahead of Print)
DOI: 10.2174/1386207322666190722162100
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