Selectivity index (SI)

Ratio of CC50 to EC50 (higher SI = better safety profile).

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Synthesis QSAR (quantitative structure-activity relationship) Heterocyclic compounds Molecular docking Nucleoside Mass spectrometry (MS) Pharmacophore Cytotoxicity binding affinity antimicrobial agents Minimum inhibitory concentration (MIC) Spirocyclic HPLC (high-performance liquid chromatography) NMR (nuclear magnetic resonance) Protecting group X-ray crystallography Enzyme inhibition Glycosylation In vitro Testing In Vivo Testing Biological Evaluation Lead Optimization Zone of Inhibition Virtual Screening Cycloaddition Catalysis Resistance Structure-Activity Relationship (SAR) Antiviral Activity Enzyme Kinetics Drug Resistance Drug Repurposing MIC Determination Bioavailability HepG2 Cells Mycobacterium tuberculosis In Silico Studies Antitubercular Agents Metabolic Stability Antifungal Activity Scaffold Hopping Toxicity Profile Bioisosteres In vitro assay Enzyme inhibition assay Prodrug Quinazolinones Docking simulation Gram-positive bacteria Gram-negative bacteria

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