| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 10598180 | Bioorganic & Medicinal Chemistry Letters | 2005 | 5 Pages |
Abstract
2-Anilino-6-phenylpyrido[2,3-d]pyrimidin-7(8H)-ones are inhibitors of c-Src and Wee1 kinases. Selectivity for c-Src was not markedly changed by 6-phenyl ring substituents, but was lowered by 5-alkyl substituents.
Keywords
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Brian D. Palmer, Jeff B. Smaill, Gordon W. Rewcastle, Ellen M. Dobrusin, Alan Kraker, Charles W. Moore, Randall W. Steinkampf, William A. Denny,
![First Page Preview: Structure-activity relationships for 2-anilino-6-phenylpyrido[2,3-d]pyrimidin-7(8H)-ones as inhibitors of the cellular checkpoint kinase Wee1 Structure-activity relationships for 2-anilino-6-phenylpyrido[2,3-d]pyrimidin-7(8H)-ones as inhibitors of the cellular checkpoint kinase Wee1](/preview/png/10598180.png)