|
|
|
题名
|
作者
|
年代
|
出处
|
被引量
|
| 1 | Potent non- steroidal progesterone receptor agonists: synthesis and SAR study of 6-aryl benzoxazines 显示文摘 | ZHANG P TEREFENKO EA FENSOME A | 2002 | Bioorg Med Chem Lett2002，12，5： | 1 |
| 2 | Design,Synthesis,and SAR of New Pyrrole-Oxindole Progesterone Receptor Modulators Leading to 5-(7-Fluoro-3,3-Dimethyl-2-Oxo-2,3-Dihydro-1H-Indol5-yl)-1-Methyl-1 H-Pyrrole-2-Carbonitrile (WAY-255348)显示文摘 | Fensome A Adams W R Adams A L | | 0，，： | 1 |
| 3 | Novel 6-aryl-1,4-dihydrobenzo oxazine-2-thiones, as potent, selective and orally active nonsteroidal progesterone receptor agonists显示文摘 | ZHANG P TEREFENKO EA FENSOME A | 2003 | Bioorg Med Chem Lett2003，13，7： | 1 |
| 4 | Synthesis and structure-activity relationship of novel 6-aryl-1,4-dihydrobeuzo oxazine -2-thiones as progesterone receptor modulators leading to the potent and selective nonsteroidal progesterone receptor agonist tanaproget显示文摘 | FENSOME A BENDER R CHOPRA R | 2005 | J Med Chem2005，48，16： | 1 |
| 5 | SAR studies of 6-'(arylamino) --4,4-disub stituted-1 -methyl-1,4-dihydro-benzo oxazin-2-ones as progesterone receptor antagonists 显示文摘 | KERN JC TEREFENKO EA FENSOME A | 2007 | Bioorg Med Chem Lett2007，17，1： | 1 |
| 6 | New progesterone receptor antagonists: 3, 3-disubstituted-5-aryloxindoles 显示文摘 | FENSOME A BENDER R COHEN J | 2002 | Bioorg Med Chem Lett2002，12，23： | 1 |
| 7 | Novel 5-aryl-1,3- dihydro-indole-2-thiones: potent, orally active progesterone receptor agonists显示文摘 | FENSOME A KOKO M WROBEL J | 2003 | Bioorg Med Chem Lett2003，13，7： | 1 |
| 8 | Synthesis and Structure Activity Relationship of Novel 6-Aryl1,4-Dihydrobenzo[d][1,3]Oxazine-2-Thiones as Progesterone Receptor Modulators Leading to the Potent and Selective Nonsteroidal Progesterone Receptor显示文摘 | Fensome A Bender R Chopra R | | 0，，： | 1 |
| 9 | SAR studies of 6-aryl-1,3-dihydrobenzimidazol-2-ones as progesterone receptor antagonists显示文摘 | TEREFENKO EA KERN J FENSOME A | 2005 | Bioorg Med Chem Lett2005，15，15： | 1 |
| 10 | On measuring electrical resistance in situ in higher plants显示文摘 | Fensom DS | 1966 | Can J Plant Sci1966，46，： | 1 |
| 11 | Acritarchs and fossil prasinophytes: An index to genera, species and infraspecific taxa 显示文摘 | Fensome R A Williams G L Barss M S | 1990 | American Association of Stratigraphic Palynologists Contribution Series1990，25，： | 1 |
| 12 | Continual production of phosphatidic acid by phospholipase D is essential for antigen-stimulated membrane ruffing in cultured mast ceils 显示文摘 | O' Luanaigh N Pardo R Fensome A | 2002 | Mol Biol Cell2002，13，10： | 1 |
| 13 | 6-Aryl-1,4-dihydro-benzooxazin-2-ones:a novel class of potent,selective,and orally active nonsteroidal progesterone receptor antagonists显示文摘 | Zhang P W Terefenko E A Fensome A | 2002 | J Med Chem2002，45，20： | 1 |
| 14 | Potent nonsteroidal progesterone receptor agonists:synthesis and SAR study of 6-arylbenzoxazines显示文摘 | Zhang P W Terefenko E A Fensome A | 2002 | Bioorg Med Chem Lett2002，12，5： | 1 |
| 15 | An essential role for phosphatidylinositol transfer protein in phospholipase c-mediated inositol lipid signaling显示文摘 | Cunningham E Fensome A | 1993 | Cell1993，74，5： | 1 |
| 16 | An Essential Role for Phosphatidylinositol Transfer Protein in Phospholipase C-mediated Inositol Lipid Signaling显示文摘 | Cunningham E Fensome A | 1993 | Cell1993，74，： | 1 |
| 17 | The application of a molecular clock based on molecular sequences and the fossil record to explain biogeographic distributions within the Alexandrium tamarense 'species complex'(Dinophyceae)显示文摘 | JOHN U FENSOME R A MEDLIN L K | 2003 | Mol Biol Evol2003，20，7： | 1 |
| 18 | Phospholipase D: a downstream effector of ARF in granulocytes显示文摘 | Cockcroft S Thomas GM Fensome A | 1994 | Science1994，263，5146： | 1 |
| 19 | SAR studies of 6-aryl- 1,3 -dihydrobenzimidazol-2 -ones as progesterone receptor antagonists显示文摘 | Terefenko E A Kern J Fensome A | 2005 | Bioorg Med Chem Lett2005，15，： | 1 |
| 20 | Nonsteroidal progesterone receptor modulators:structure activity relationships显示文摘 | Winneker R C Fensome A Wrobel J E | | 0，，01： | 1 |
您所在的机构暂未开通此部分的功能，请联系管理员