Gul, SergenAcikgoz, EdaCakir, MustafaMenges, Nurettin2025-05-102025-05-1020242470-134310.1021/acsomega.3c098222-s2.0-85194489772https://doi.org/10.1021/acsomega.3c09822https://hdl.handle.net/20.500.14720/10764Excited-state intramolecular proton transfer (ESIPT)-based fluorescent molecules offer several exciting applications and are utilized most frequently as a cell imaging agent. Because of this, four distinct imidazole derivatives with ESIPT emission have been synthesized, and their fluorescence characteristics have been assessed in a variety of settings. Measurements using fluorescence spectroscopy have shown a promising candidate for cell staining, and potential candidate was specifically investigated for cell imaging uses in HT-29, MDA-MB-231, and HaCaT. Cytotoxicity of candidate molecule (1d) was analyzed using HT-29 and HaCaT cell lines, and at a dosage of 160 mu M, HT-29 and HaCaT cell lines showed no signs of important cell toxicity. When spectroscopically measured, compound 1d showed no fluorescence ability in phosphate-buffered saline (PBS) solution. However, after 8 h of incubation in several cell lines, excellent fluorescence characteristics were seen in the green and red filters.eninfo:eu-repo/semantics/openAccessDesign and Synthesis of Esipt-Based Imidazole Derivatives for Cell ImagingArticle923Q2Q2242912429838882084WOS:001233186700001