|
|
|
题名
|
作者
|
年代
|
出处
|
被引量
|
| 1 | Identification of N-(4-piperidinyl)-4-(2,6-dichlorobenzoylamino)-1H-pyrazole-3-carboxamide(AT7519),a novel cyclin dependent kinase inhibitor using fragmentbased X-ray crystallography and structure based drug design显示文摘 | WYATT P G WOODHEAD A J BERDINI V | 2008 | J Med Chem2008，51，16： | 1 |
| 2 | Identification of N-(4-Piperidinyl)-4-(2,6-dichlorobenzoylamino)-1 H-pyrazole-3-carboxamide (AT7519),a Novel Cyclin Dependent Kinase Inhibitor Using Fragment-Based X-Ray Crystallography and Structure Based Drug Design+显示文摘 | Wyatt P G Woodhead A J Berdini V | | 0，，16： | 1 |
| 3 | Fragment-based discovery of the pyrazol-4-yl urea (AT9283), a multitargeted kinase inhibitor with potent Aurora kinase activity 显示文摘 | Howard S Berdini V Boulstridge J A | 2008 | J Med Chem2008，52，2： | 1 |
| 4 | Fragment- based discovery of the pyrazol-4-yl urea (AT9283),a multi-targeted kinase inhibitor with potent aurora kinase activity 显示文摘 | HOWARD S BERDINI V BOULSTRIDGE J A | 2009 | J Med Chem2009，52，2： | 1 |
| 5 | Fra- gment based discovery of the pyra-4-yl-urea ( AT9283 ) , a muhitargeted kinase inhibitor with potent aurora kinase activity显示文摘 | HOWARD S BERDINI V BOULSTRIDGE J A | 2009 | J Med Chem2009，52，2： | 1 |
| 6 | Frag- ment-based discovery of the pyrazol-4-yl urea ( AT9283 ) , a mul- titargeted kinase inhibitor with potent aurora kinasc activity 显示文摘 | HOWARD S BERDINI V BOULSTRIDGE JA | 2009 | J Med Chem2009，52，2： | 1 |
| 7 | Identifica- tion of N-( 4-piperidinyl ) -4-( 2, 6-dichlorobenzoylamino ) -1H- pyrazole-3-carboxamide (AT7519 ) , a novel cyelin dependent ki- nase inhibitor using fragment-based X-ray crystallography and structure based drug design显示文摘 | WYATT PG WOODHEAD AJ BERDINI V | 2008 | J Med Chem2008，51，16： | 1 |
| 8 | Fragment-based discovery of the pyrazol4-yl urea (AT9283) , a multitargeted kinase inhibitor with potent aurora kinase activity 显示文摘 | HOWARD S BERDINI V BOULSTRIDGE J A | 2009 | J Med Chem2009，52，2： | 1 |
| 9 | I- dentification of N-( 4-piperidinyl )-4-( 2, 6-dichloro- benzoyl-amino)-lH-pyrazole-3-carboxamide (AT7519), a novel cyclin dependent kinase inhibitor using fragment- based X-ray crystallography and structure based drug design显示文摘 | WYATT P G WOODHEAD A J BERDINI V | 2008 | J Med Chem2008，51，16： | 1 |
| 10 | BouIstridge identification of N-( 4-Piperidinyl ) -4-( 2,6-dichlorobenzoylamino)-lH-pyrazole-3-carboxamide (AT7519) , a novel cyclin dependent kinase inhibitor using fragment-based X-Ray crystallog- raphy and structure based drug design 显示文摘 | WYATT PG WOODHEAD A J BERDINI V | 2008 | J Med Chem2008，51，16： | 1 |
| 11 | One-pot, new stereoselective synthesis of endo-tropanamine显示文摘 | Allegretti M Berdini V Cesta MC | 2001 | Tetrahedron Lett2001，42，25： | 1 |
| 12 | Identification of inhibitors of protein kinase B using fragment-based lead discovery 显示文摘 | Saxty G Woodhead S J Berdini V | 2007 | J Med Chem2007，50，： | 1 |
| 13 | Fragment-based discovery of potent and selective DDR1/2 inhibitors 显示文摘 | MURRAY C W BERDINI V BUCK I M | 2015 | ACS Medicinal Chemistry Letters2015，6，7： | 1 |
| 14 | Fragment- based discovery of the pyrazol-4-yl urea ( AT9283 ), a muhitarget- ed kinase inhibitor with potent aurora kinase activity 显示文摘 | HOWARD S BERDINI V BOULSTRIDGE JA | 2009 | J Med Chem2009，52，2： | 1 |
| 15 | Fragment-based dis- covery of the pyrazol-4-yl urea ( AT9283 ) ,a multitargeted kinase inhibitor with potent aurora kinase activity 显示文摘 | Howard S Berdini V Boulstridge JA | 2008 | J Med Chem2008，52，2： | 1 |
| 16 | Fragment-based discovery of the pyrazol-4-yl urea (AT9283), a multitargeted kinase inhibitor with potent aurora kinase activity显示文摘 | Howard S Berdini V Boulstridge J A | 2009 | J Med Chem2009，52，： | 1 |
您所在的机构暂未开通此部分的功能，请联系管理员