Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1371790 | Bioorganic & Medicinal Chemistry Letters | 2012 | 4 Pages |
3-Phosphoinositide-dependent protein kinase-1 (PDK1) has been recognized as a promising anticancer target. Thus, it is interesting to identify new inhibitors of PDK1 for anticancer drug discovery. Through a combined use of virtual screening and wet experimental activity assays, we have identified a new PDK1 inhibitor with IC50 = ∼200 nM. The anticancer activities of this compound have been confirmed by the anticancer activity assays using 60 cancer cell lines. The obtained new PDK1 inhibitor and its PDK1-inhibitor binding mode should be valuable in future de novo design of novel, more potent and selective PDK1 inhibitors for future development of anticancer therapeutics.
Graphical abstractA combined use of virtual screening and wet experimental activity assays has led to identification of a new inhibitor of 3-phosphoinositide-dependent protein kinase-1 (PDK1) with IC50 = ∼200 nM.Figure optionsDownload full-size imageDownload as PowerPoint slide