摘要
Insulin-like growth factor-1 receptor (IGF-IR) 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-IR 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.
| 源语言 | 英语 |
|---|---|
| 页(从-至) | 2661-2665 |
| 页数 | 5 |
| 期刊 | Journal of Medicinal Chemistry |
| 卷 | 53 |
| 期 | 6 |
| DOI | |
| 出版状态 | 已出版 - 25 3月 2010 |
| 已对外发布 | 是 |
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