Abstract
AbstractChemical transformation study is considered as an important tool for new drugs discovery. It was conducted on the natural compound eugenol for semi‐synthesizing new structural scaffolds. Three new eugenol 1,2,3‐triazole derivatives as well as a known one were synthesizedviaclick chemistry using the Cu(I)‐catalyzed azide–alkyne 1,3‐dipolar cycloaddition method. All derivatives were characterized by NMR analysis in combination with ESIMS. Molecular docking andin vitroinhibition potency of eugenol and its derivatives towards hyaluronidase enzyme were examined. The synthesized derivative 4‐((4‐allyl‐2‐methoxyphenoxy)methyl)‐1‐benzyl‐1H‐1,2,3‐triazole showed an enhanced hyaluronidase inhibitory effect, 1.5 times, higher than its parent compound eugenol.
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