Abstract
A series of novel hedgehog signaling pathway inhibitors have been designed and synthesized based on our previously reported scaffold of 4-(2-pyrimidinylamino)benzamide. The Hh signaling pathway inhibitory activities were evaluated by Gli-luciferase reporter method and most compounds showed more potent inhibitory activities than vismodegib. Three compounds were picked out to evaluated in vivo for their PK properties, and compound 23b bearing a 2-pyridyl A-ring and (morpholin-4-yl)methylene at 3-position of D-ring demonstrated satisfactory PK properties. This study suggested the 4-(2-pyrimidinylamino)benzamides were a series of potent Hh signaling pathway inhibitors, deserving to further structural optimization.
| Original language | English |
|---|---|
| Pages (from-to) | 5029-5036 |
| Number of pages | 8 |
| Journal | Bioorganic and Medicinal Chemistry |
| Volume | 26 |
| Issue number | 18 |
| DOIs | |
| State | Published - 1 Oct 2018 |
Keywords
- 4-(2-Pyrimidinylamino)benzamide
- Hedgehog signaling pathway inhibitors
- In vivo
- SAR
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