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: | , |
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| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
Frontiers Media S.A.
2024-07-01
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| Schriftenreihe: | Frontiers in Drug Discovery |
| Schlagworte: | |
| Online-Zugang: | https://www.frontiersin.org/articles/10.3389/fddsv.2024.1424402/full |
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