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Structure-activity models of oral clearance, cytotoxicity, and LD50: a screen for promising anticancer compounds
BACKGROUND: Quantitative structure-activity relationship (QSAR) models have become popular tools to help identify promising lead compounds in anticancer drug development. Few QSAR studies have investigated multitask learning, however. Multitask learning is an approach that allows distinct but relate...
| Autores principales: | , |
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| Formato: | Texto |
| Lenguaje: | English |
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BioMed Central
2008
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2442056/ https://www.ncbi.nlm.nih.gov/pubmed/18554402 http://dx.doi.org/10.1186/1471-2210-8-12 |