Synthesis, molecular docking, QSTR and in?silico ADME studies of novel 1,3?thiazolidine?amide derivatives as hybrid bioactive heterocycles
Chemical Biology and Drug Design
JANUARY 29, 2024
A series of 1,3-thiazolidine- amide derivatives were synthesized via two different methods (microwave irradiation and conventional). These derivatives exhibited in vitro good to excellent antimicrobial activity. Molecular docking study performed on the crucial antifungal target 4WMZ. Quantitative structure toxicity relationship (QSTR) study pointed out the slight toxic nature of compounds.
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