Synthesis, Antibacterial Evaluation, and Molecular Docking Investigations of Biologically Active Substituted Tetrazole-Linked 1,8-Naphthyridine Derivatives
Pyrazole-1,3,4-thiadiazine-linked isoxazole derivatives, specifically 6n and 6o, are identified as potential candidates for the development of novel antibacterial and antibiofilm drugs.
Reddycherla Venkatesh, K. Chennakesavulu, Reddy G. Ramanjaneya· Current Organic Synthesis· 0 citations
Compounds S6 and S1 showed the highest activity, possibly due to the thiazole nucleus linked to furan and substituted aromatic rings, and the experimental findings were consistent with the in silico molecular docking results.
Chandravadivelu Gopi, M. Dhanaraju, Eethakota Parimala Naga Devi et al.· Asian Journal of Chemistry· 0 citations
The results suggest that the 2,4-dichlorophenyl–1,2,3-triazole scaffold represents a promising starting point for further optimization, with antimicrobial activity governed by a balance between electronic properties and physicochemical factors influencing membrane permeability.
Mohammed Sallam, A. Hassan, A. Y. Alzahrani et al.· Scientific Reports· 0 citations
A series of new indole-pyrazole-linked isoxazole hybrids (5a-o) were synthesized using Cu(I)-catalyzed 1,3-dipolar cycloaddition and assessed for antibacterial and antibiofilm activities against methicillin-sensitive Staphylococcus aureus (MSSA), methicillin-resistant Staphylococcus aureus (MRSA) and vancomycin-resista...
Venkatesh Reddycherla, K. Chennakesavulu, G. R. Reddy et al.· Asian Journal of Chemistry· 0 citations
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