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4-aminoantipyrine derivative 1 is a fluorescent substituted aromatic carbonyl compound synthesized via the condensation of fluorine-substituted benzoyl chlorides with 4-aminoantipyrine. It exhibits significant fluorescence emission and has demonstrated potent in vitro cytotoxic activity against human cervical cancer cells (SiHa) with an IC50 of 0.912 μM, comparable to Pazopanib. Molecular docking studies suggest its potential anticancer activity is mediated through interactions with the HPV16-E7 target protein.
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