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25篇 您的检索式:作者名="PENNING TD"
    题名 作者 年代 出处 被引量
1Synthesis and biological evaluation of the 1,5-diarylpyrazole class of cyclooxygenase2 inhibitors: identification of 4- benzenesulfonamide(SC-58635, Celecoxib)显示文摘Penning TD Talley J J Bertenshaw SR 1997J Med Chem1997,40,9:1
2Synthesis and biological evaluation of the 1,5-diarylpyrazole class of cyclooxygenase-2 inhibitors: identification of 4-benze nesulfonamide (SC-58635, celecoxib) 显示文摘Penning TD Talley J J Bertenshaw SR 1997J Med Chem1997,40,9:1
3Synthesis of potent leukotriene A(4) hydrolase inhibitors identification of 3-(methyl (3-(4-(phenylmethyl) phenoxy) propyl) amino) propanoic acid 显示文摘Penning TD Russel MA Chen BB 2002J Med Chem2002,45,:1
4Synthesis and biological evaluation of the 1,5-diarylpyrazole class of cyclooxygenase-2 inhibitors:identification of 4- benze nesulfonamide (SC-58635,celecoxib)显示文摘Penning TD Talley JJ Bertenshaw SR 1997J Med Chem1997,40,:1
5ABT-888,an orally active poly (ADP-ribose) polymerase inhibitor that potentiates DNA-damaging agents in preclinical tumor models显示文摘Donawho CK Luo Y Penning TD 0,,:1
6Synthesis and biological evaluation of the 1,5-diarylpyrazole class of cyclooxygenase-2 inhibitors:identification of 4- benzenesulfonamide(SC-58635,celecoxib)显示文摘Penning TD Tally JJ Bertenshaw SR 1997J Med Chem1997,40,9:1
7Discovery of the Poly(ADP- ribose) polymerase (PARP) inhibitor 2--lH-benzimidazole-4-carboxamide (ABT-888) for the treat- ment of cancer 显示文摘Penning TD Zhu GD Gandhi VB 2009J Med Chem2009,52,2:1
8ABT-888,an orally active poly(ADP-ribose) polymerase inhibitor that potentiates DNA-damaging agents in preclinical tumor models显示文摘Donawho CK Luo Y Penning TD 2007Clin Cancer Res2007,13,9:1
9Synthesis and biological evaluation of the 1,5-diarylpyrazole class of cyclooxy-genase-2 inhibitors:identification of 4-显示文摘Penning TD Talley JJ Bertenshaw SR 1997J Med Chem1997,40,:1
10Synthesis and biological evaluation of the 1 5-diarylpyrazole class of cyclooxygenase2 inhibitors:identification of 4-[ 5-(4-methylphenyl)-3-( trifluoromethyl)-1H-pyrazol-1-yl] benze nesulfonamide (SC-58635 celecoxib)显示文摘Penning TD Talley JJ Bertenshaw SR 0,,:1
11ABT-888, an orally active poly (ADP-ribose) polymerase inhibitor that potentiates DNA-damaging agents in preclinical tumor models 显示文摘Donawho CK Luo Y Penning TD 2007Clin Cancer Res2007,13,9:1
12Synthesis and biological evaluation of the 1,5-diarylpyrazole class of cyclooxygenase-2 inhibitors:identification of 4-显示文摘Penning TD Talley JJ Bertenshaw SR 1997J Med Chem1997,40,:1
13Synthesis and biological evaluation of the 1,5-diarylpyrazole class of cyclcooxygenuse-2 inhibitors: identification of 4-显示文摘Penning TD Talley JJ Berteushaw SR 1997J Med Chem1997,40,9:1
14Synthesis and Biolo- gical Evaluation of the 1,5-Diarylpyrazole Class of Cyclooxygenase-2 of 4-benzenesulfonamide (SC-58635,Celecoxib)显示文摘Penning TD Talley JJ Bertenshaw SR 1997J Med Chem1997,40,9:1
15Synthesis and biological evaluaton of the 1,5-diarylpyrazole class of cyclooxygenase-2 inhibitor: Identification of 4- benzenesulfona mide(SC-58635, Celecoxib)显示文摘Penning TD Talley JJ Bertenshaw SR 1997J Med Chem1997,40,9:1
16Inhibitors of leukotriene A4 (LTA4) hydrolase as potential anti-inflammatory agents 显示文摘Penning TD 2001Curr Pharm Des2001,7,:1
17Synthesis of imidazopyridines and purines as potent inhibitors of leukotriene A4 hydrolase 显示文摘Penning TD Chandrakumar NS Desai BN 2003Bioorg Med Chem Lett2003,13,:1
18ABT-888,an orally active poly(ADP-ribose)polymer-ase inhibitor that potentiates DNA-damaging a-gents in preclinical tumor models显示文摘Donawho CK Luo Y Penning TD 2007Clin Cancer Res2007,13,9:1
19Structure- activity relationship studies on 1- pyrrolidine (SC-22716), a potent inhibitor of leukotriene A4 (LTA4) hydrolase 显示文摘Penning TD Chandrakumar NS Chen BB 2000J Med Chem2000,43,4:1
20Synthesis and biological evaluation of the 1,5-diarylpyrazole class of cyclooxygenase-2 inhibitors 显示文摘 Talley JJ Bertenshaw SR 1997J Med Chem1997,40,9:1
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