Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1372837 | Bioorganic & Medicinal Chemistry Letters | 2008 | 5 Pages |
Abstract
This communication describes the discovery of a novel series of Aurora kinase inhibitors. Key SAR and critical binding elements are discussed. Some of the more advanced analogues potently inhibit cellular proliferation and induce phenotypes consistent with Aurora kinase inhibition. In particular, compound 21 (SNS-314) is a potent and selective Aurora kinase inhibitor that exhibits significant activity in pre-clinical in vivo tumor models.
Graphical abstractThe discovery of a novel series of Aurora kinase inhibitors is disclosed.Figure optionsDownload full-size imageDownload as PowerPoint slide
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Johan D. Oslob, Michael J. Romanowski, Darin A. Allen, Subramanian Baskaran, Minna Bui, Robert A. Elling, William M. Flanagan, Amy D. Fung, Emily J. Hanan, Shannon Harris, Stacey A. Heumann, Ute Hoch, Jeffrey W. Jacobs, Joni Lam, Chris E. Lawrence,