Abstract
Insulin-like growth factor-1 receptor (IGF-1R) is a growth factor receptor tyrosine kinase acting as a critical mediator of cell proliferation and survival. Novel 5-benzylidenethiazolidine-2,4-dione (5) and 5-(furan-2-ylmethylene)thiazolidine-2,4-dione (6) compounds were identified as potent and selective IGF-1R inhibitors via hierarchical virtual screening. Initial SAR and biological activity of the analogues of 5 and 6 with thiazolidine-2,4-dione template are presented, and several inhibitors with low nanomolar potency are reported.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Binding, Competitive
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Cell Line, Tumor
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Cell Proliferation / drug effects
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Drug Discovery / methods*
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Humans
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Inhibitory Concentration 50
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Models, Molecular
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Molecular Structure
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Protein Kinase Inhibitors / chemistry
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Protein Kinase Inhibitors / metabolism
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Protein Kinase Inhibitors / pharmacology*
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Protein Structure, Tertiary
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Receptor, IGF Type 1 / antagonists & inhibitors*
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Receptor, IGF Type 1 / chemistry
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Receptor, IGF Type 1 / metabolism
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Stereoisomerism
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Structure-Activity Relationship
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Thiazolidinediones / chemistry
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Thiazolidinediones / metabolism
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Thiazolidinediones / pharmacology*
Substances
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Protein Kinase Inhibitors
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Thiazolidinediones
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thiazolidine-2,4-dione
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Receptor, IGF Type 1