Bingül, MuratŞenkuytu, ElifSağlam, Mehmet TurgutBoga, MehmetKandemir, HakanŞengül, İbrahim Fazıl2022-05-112022-05-1120190922-61681568-5675https://doi.org/10.1007/s11164-019-03844-xhttps://hdl.handle.net/20.500.11776/7293Utilizing Schiff base condensation of the 9-ethylcarbazole-3,6-dicarbaldehyde and thiosemicarbazides, four new N-ethylcarbazole-based bis-thiosemicarbazone compounds 4a-d were successfully synthesized in high yields. The photophysical properties of the targeted compounds 4a-d were investigated using UV-vis absorption and fluorescence emission spectroscopy. The antioxidant properties of targeted compounds 4a-d were determined by DPPH radical scavenging, ABTS Cation Radical Decolarization and CUPRAC Cupric Reducing Antioxidant Capacity assay methods. Moreover, the anti-cholinesterase properties of designated compounds were investigated by the Acetylcholinesterase (Ach) and Butyrylcholinesterase (BCh) enzyme inhibition assays. The compound 4a was determined as a valuable candidate to be a potent antioxidant agent for the DPPH and ABTS assays. The compound 4d was found to be a target compound for the kinetic measurements to identify the mechanism of action in the area of anticholinesterase activity assay.en10.1007/s11164-019-03844-xinfo:eu-repo/semantics/closedAccessCarbazoleThiosemicarbazoneAntioxidant activitiesPhotophysical propertiesLigand SynthesisFluorescenceDerivativesCopper(Ii)ComplexesIronArticle45944874499Q3WOS:0004818050000162-s2.0-85065244657Q2