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Lead identification to generate 3-cyanoquinoline inhibitors of insulin-like growth factor receptor (IGF-1R) for potential use in cancer treatment.

Authors :
Miller LM
Mayer SC
Berger DM
Boschelli DH
Boschelli F
Di L
Du X
Dutia M
Floyd MB
Johnson M
Kenny CH
Krishnamurthy G
Moy F
Petusky S
Tkach D
Torres N
Wu B
Xu W
Source :
Bioorganic & medicinal chemistry letters [Bioorg Med Chem Lett] 2009 Jan 01; Vol. 19 (1), pp. 62-6. Date of Electronic Publication: 2008 Nov 17.
Publication Year :
2009

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.

Details

Language :
English
ISSN :
1464-3405
Volume :
19
Issue :
1
Database :
MEDLINE
Journal :
Bioorganic & medicinal chemistry letters
Publication Type :
Academic Journal
Accession number :
19041240
Full Text :
https://doi.org/10.1016/j.bmcl.2008.11.037