摘要
In our efforts to minimize the side effects associated with low selectivity against the other PDE isozymes, a novel class of 2-phenylquinazolin-4(3H)-one derivatives were designed and prepared as potent PDE5 inhibitors with high selectivity against PDE6. The syntheses and SAR studies of such molecules were reported.
| 原文 | English |
|---|---|
| 頁(從 - 到) | 2777-2779 |
| 頁數 | 3 |
| 期刊 | Bioorganic and Medicinal Chemistry Letters |
| 卷 | 19 |
| 發行號 | 10 |
| DOIs | |
| 出版狀態 | Published - 15 5月 2009 |
| 對外發佈 | 是 |
指紋
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