The role of physicochemical and topological parameters in drug design

Quantitative structure activity relationship (QSAR) is a widely used tool in rational drug design that establishes relationships between the physicochemical and topological descriptors of ligands and their biological activities. Obtained QSAR models help identify descriptors that play pivotal roles...

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Hauptverfasser: Janki Darlami (Verfasst von), Shweta Sharma (Verfasst von)
Format: Buch
Veröffentlicht: Frontiers Media S.A., 2024-07-01T00:00:00Z.
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