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Synthesis, Characterisation, Cytotoxicity, Antimicrobial and Docking Studies of (2,4-Bis((1-phenyl-1H-1,2,3-triazol-4-yl)methoxy)phenyl)(phenyl)methanone Derivatives
Corresponding Author(s) : Bolisetti Venkateswarlu
Asian Journal of Chemistry,
Vol. 38 No. 7 (2026): Vol. 38, No 7 (2026)
Abstract
Using a copper(I)-catalysed azide-alkyne (CuAAC) cycloaddition method, a new series of 2,4-bis((1-phenyl-1H-1,2,3-triazol-4-yl)-methoxy)phenyl)(phenyl)methanone analogues (7a-o) were synthesised, characterised by 1H and 13C NMR, FT-IR, mass and elemental analysis and evaluated for the biological activities. Cell viability method on MCF-7, HeLa and PC-3 cells revealed compounds 7d, 7j and 7f exhibited potent cytotoxicity, while other compounds displayed moderate to weak effects, indicating promising anticancer potential for selected derivatives. Antibacterial and antifungal activities were tested using disc diffusion method, among the tested compounds 7d, 7f and 7k showed strong activity, outperforming streptomycin and amphotericin B. Molecular docking against 17β-HSD1 demonstrated high binding affinities for 7j (-12.4 kcal/mol) and 7d (-12.3 kcal/mol), superior to doxorubicin (-8.9 kcal/mol), forming interactions with key residues like ILE14 and SER142. These findings suggest the synthesised compounds are promising anticancer and antimicrobial agents.
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