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AIMS: polymerase. MATERIALS & METHODS: polymerase, where the model with optimized synthetic accessibility and structural complexity was subjected to docking and molecular dynamics simulations and pharmacokinetic prediction. RESULTS: Among 1,722 new forms, the Hit-960 compound stood out for its high bioaffinity and stability, with a binding energy of -9.12 kcal/mol and 75% synthetic accessibility. CONCLUSIONS: infections.
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Pinto et al. (2025) studied this question.
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