Synthesis and antifungal activity of novel 1,2,4-triazolyl coumarins (CROSBI ID 735388)
Prilog sa skupa u zborniku | sažetak izlaganja sa skupa
Podaci o odgovornosti
Karnaš, Maja ; Vrandečić, Karolina ; Ćosić, Jasenka ; Rastija, Vesna ; Agić, Dejan ; Šubarić, Domagoj ; Molnar, Maja
engleski
Synthesis and antifungal activity of novel 1,2,4-triazolyl coumarins
Coumarins and triazoles are two interesting groups of heterocyclic compounds, both exhibiting a wide range of biological activities. The joining of these two scaffolds into a hybrid compound with the improved activities has already been reported. [1] In this research, 11 new hybrid compounds were synthesized, utilizing a deep eutectic solvent as an environmentally sustainable method of organic synthesis. Compounds were obtained in good yields through a one-step reaction of coumarinyl hydrazides and various substituted isothiocyanates, without the use of catalysts. [2] Since many commercially available fungicides are based on triazole derivatives, antifungal activity of 1, 2, 4-triazolyl coumarins was evaluated in vitro on two pathogenic fungi, Fusarium oxysporum and Fusarium culmorum. The tested compounds moderately inhibited the mycelial growth of F. oxysporum (35.0-57.5%), but were mostly ineffective against F. culmorum. Compound 1b, as the most potent growth inhibitor, was further analyzed computationally. A molecular docking analysis was performed to evaluate the binding mode of compound 1b with sterol 14 α-demethylase, the target enzyme of triazole based fungicides
coumarines ; triazoles ; antifungal activity ; deep eutectic solvent
nije evidentirano
nije evidentirano
nije evidentirano
nije evidentirano
nije evidentirano
nije evidentirano
Podaci o prilogu
83-83.
2023.
objavljeno
Podaci o matičnoj publikaciji
Rogošić, Marko
Zagreb: Hrvatsko društvo kemijskih inženjera i tehnologa (HDKI)
Podaci o skupu
28th Croatian Meeting of Chemists and Chemical Engineers
poster
28.03.2023-01.04.2023
Rovinj, Hrvatska