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QSAR-derived affinity fingerprints (part 2): modeling performance for potency prediction
Affinity fingerprints report the activity of small molecules across a set of assays, and thus permit to gather information about the bioactivities of structurally dissimilar compounds, where models based on chemical structure alone are often limited, and model complex biological endpoints, such as h...
Sparad:
| I publikationen: | J Cheminform |
|---|---|
| Huvudupphovsmän: | , , , |
| Materialtyp: | Artigo |
| Språk: | Inglês |
| Publicerad: |
Springer International Publishing
2020
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| Ämnen: | |
| Länkar: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7339533/ https://ncbi.nlm.nih.gov/pubmed/33431016 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13321-020-00444-5 |
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