Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1375916 | Bioorganic & Medicinal Chemistry Letters | 2009 | 5 Pages |
Abstract
Insulin-like growth factor receptor (IGF-1R) is a growth factor receptor tyrosine kinase that acts as a critical mediator of cell proliferation and survival. Inhibitors of this receptor are believed to provide a new target in cancer therapy. We previously reported an isoquinolinedione series of IGF-1R inhibitors. Now we have identified a series of 3-cyanoquinoline compounds that are low nanomolar inhibitors of IGF-1R. The strategies, synthesis, and SAR behind the cyanoquinoline scaffold will be discussed.
Gaphical abstractThe strategies, synthesis, and SAR behind novel cyanoquinoline IGFR inhibitors (1) are reported.Figure optionsDownload full-size imageDownload as PowerPoint slide
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Lori M. Miller, Scott C. Mayer, Dan M. Berger, Diane H. Boschelli, Frank Boschelli, Li Di, Xuemei Du, Minu Dutia, Middleton B. Floyd, Mark Johnson, Cynthia Hess Kenny, Girija Krishnamurthy, Franklin Moy, Susan Petusky, Diane Tkach, Nancy Torres, Biqi Wu,