Three-Dimensional-QSAR and Relative Binding Affinity Estimation of Focal Adhesion Kinase Inhibitors
Three-Dimensional-QSAR and Relative Binding Affinity Estimation of Focal Adhesion Kinase Inhibitors
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Switzerland: MDPI AG
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English
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Switzerland: MDPI AG
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Precise binding affinity predictions are essential for structure-based drug discovery (SBDD). Focal adhesion kinase (FAK) is a member of the tyrosine kinase protein family and is overexpressed in a variety of human malignancies. Inhibition of FAK using small molecules is a promising therapeutic option for several types of cancer. Here, we conducted...
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Three-Dimensional-QSAR and Relative Binding Affinity Estimation of Focal Adhesion Kinase Inhibitors
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TN_cdi_doaj_primary_oai_doaj_org_article_9cef4d8a365840818ad8e747bc3f0f6b
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https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_9cef4d8a365840818ad8e747bc3f0f6b
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ISSN
1420-3049
E-ISSN
1420-3049
DOI
10.3390/molecules28031464