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70篇 您的检索式:作者名="Gangjee A"
    题名 作者 年代 出处 被引量
1Synthesis of classical,three-carbon-bridged 5-substituted furopyrimidine and 6-substituted pyrrolopyrimidine analogues as antifolates显示文摘Gangjee A Zeng Y McGuire JJ 2004J Med Chem2004,47,27:1
2Synthesis and evaluation of a classical 2,4-diamino-5-substitutedfuropyrimidine and 2-amino-4-oxo-6-substitutedpyrrolopyrimidine as antifolates显示文摘Gangjee A Yang J McGuireb JJ 2006Bioorg Med Chem2006,14,24:1
3Synthesis of N-4-pyrimidin-6-yl) thio]benzoyl-L-glutamic acid and N-4-pyrimidin-6 -yl) thio]benzoyl-L-glutamic acid as dual inhibitors of dihydrofolate reductase and thymidylate synthase and as potential antitumor agents显示文摘Gangjee A Lin X Kisliuk RL 2005J Med Chem2005,48,23:1
4Dual inhibitors of thymidylate synthase and dihydrofolate reductase as antitumor agents:design,synthesis,and biological evaluation of classical and nonclassical pyrrolopyrimidine antifolates显示文摘Gangjee A Jain DH Phan J 2006J Med Chem2006,49,3:1
5Recent advances in classical and non-classicalantifolates as antitumor and antiopportunistic infection agents显示文摘GANGJEE A JAIN H KURUP S 2007Anti-cancer Agents Med Chem2007,7,5:1
6Synthesis of classical, four-carbon bridged 5-substituted furo pyrimidine and 6-substituted pyrrolo pyrimidine analogues as antifolates显示文摘GANGJEE A ZENG YB MCGUIRE JJ 2005J Med Chem2005,48,16:1
7Classical and nonclassical furo pyrimidines as novel antifolates : synthesis and biological activities 显示文摘GANGJEE A DEVRAJ R MCGUIRE JJ 1994J Med Chem1994,37,8:1
8Design, synthesis, and biological evaluation of 2,4-diamino-5-methyl-6-substituted-pyrrolo pyrimidines as dihydrofolate reductase inhibitors 显示文摘Gangjee A Lin X Sherry F 2004J Med Chem2004,47,:1
9Recent advances in classical and non-classical antifolates as antitumor and antiopportunistic infec- tion agents: Part Ⅱ 显示文摘Gangjee A Jain HD Kurup S 2008Anticancer Agents Med Chem2008,8,2:1
10Synthesis of classical and a nonclassical 2-amino-4-oxo-6-methyl-5-substituted pyrrolo pyrimidine antifolate inhibitors of thymidylate synthase显示文摘GANGJEE A MAVANDADI F KISLIUK R L 1999Med Chem1999,42,:1
11Synthesis of N-14- pyrimidin46-yl) thio ] ben-zoyl t -L-glutamic acid and N- 1 4- pyrimidin-6-yl )thio] benzoylt-L-glutamic acid as dual inhibitors of dihydrofolate reductase and thymidylate synthase and as potential antitumor agents显示文摘GANGJEE A LIN X KISLIUK RL 2005J Med Chem2005,48,23:1
12Design,synthesis,and x-ray crystal structure of A potent dual inhibitor of thymidylate synthase and dihydrofolate reductase as an antitumor agent显示文摘GANGJEE A YU J MCGUIRE J J 2000J Med Chem2000,43,:1
13Effect of bridge region variation on antifolate and antitumor activity of classical 5-substituted 2,4-diaminofuro pyrimidines 显示文摘GANGJEE A DEVRAJ R MCGUIRE JJ 1995J Med Chem1995,38,19:1
14Design and synthesis of classical and nonclassical 6-arylthio-2,4 -diamino-5-ethylpyrrolopyrimidines as antifolates显示文摘Gangjee A Zeng YB Talreja T 2007J Med Chem2007,50,13:1
15Design and synthesis of classical and nonclassical 6-arylthio-2,4- diamino-5-ethylpyrrolo pyrimidines as antifolates 显示文摘Gangjee A Zeng Y Talreja T J 2007J Med Chem2007,50,:1
16Design, synthesis,and X-ray crystal structure of a potent dual inhibitor of thymidylate synthase and dihydrofolate reductase as an antitumor agent显示文摘GANGJEE A YU J MCGUIRE JJ 2000J Med Chem2000,43,21:1
17Novel 5-substituted,2,4-diaminofuropyrimidines as multireceptor tyrosine kinase and dihydrofolate reductase inhibitors with antiangiogenic and antitumor activityq显示文摘Gangjee A Zeng YB Ihnat M 2005Bioorg Med Chem2005,13,18:1
18The effect of 5-alkyl modification on the biological activity of pyrrolo pyrimidine containing classical and non- classical antifolates as inhibitors of dihydrofolate reductase and as antitumor and/or antiopportunistic infection agents显示文摘Gangjee A Hiteshkumar D Queener S F 2008J Med Chem2008,51,:1
19Design, synthesis,and biological activities of classical N-{4- pyrimidln-5 -yl ) ethyl ] henzoyl} -L-glutamic acid and its 6-methyl derivative as potential dual inhibitors of thymidylate synthase and dihydrofolate reductase and as potential antitumor agents显示文摘GANGJEE A YU J KISLIUK RL 2003J Med Chem2003,46,4:1
20Novel non-classical C9-methyl-5-substituted-2,4-diaminopyrrolo-pyrimidines as potential inhibitors of dihydrofolate reductase and as anti-opportunistic agents显示文摘Gangjee A Yanga J Queenerb SF 2006Bioorg Med Chem2006,14,24:1
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