Cakmak, SukriyeAycan, TugbaYakan, HasanVeyisoglu, AyselTanak, HasanEvecen, Meryem2025-03-232025-03-2320232053-2296https://doi.org/10.1107/S2053229623003418https://hdl.handle.net/11486/5440N-[(4-Fluorophenyl)sulfanyl]phthalimide (C14H8FNO2S, FP) was synthesized and characterized using X-ray crystallography. It was then investigated via quantum chemical analysis using the density functional theory (DFT) approach, as well as spectrochemically using FT-IR and H-1 and C-13 NMR spectroscopy, and elemental analysis. The observed and stimulated spectra are in very good agreement for the DFT method. The in vitro antimicrobial activity of FP against three Gram-positive bacteria, three Gram-negative bacteria and two fungi were determined using the serial dilution method, and FP showed the highest anti-bacterial activity against E. coli, with a MIC of 128 mu g ml(-1). Druglikeness, ADME (absorption, distribution, metabolism and excretion) and toxicology studies were carried out to theoretically examine the drug properties of FP.eninfo:eu-repo/semantics/closedAccesssulfenimidephthalimideXRDantimicrobial activityspectroscopic studiesADMETcrystal structurePreparation, spectroscopic, X-ray crystallographic, DFT, antimicrobial and ADMET studies of N-[(4-flourophenyl)sulfanyl]phthalimideArticle79249+10.1107/S2053229623003418372224202-s2.0-85163914244N/AWOS:001004162600005Q3