國家衛生研究院 NHRI:作者相关文件

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"Li, WT"的相关文件

类别	日期	题名	關聯
[吳綺容] 期刊論文	2022-01-04	Clinical and microbiological characteristics of culture-positive, influenza-associated pulmonary aspergillosis: A single-center study in Southern Taiwan, 2016-2019	-
[夏克山] 期刊論文	2016-01	Synthesis of (E)-oxindolylidene acetate using tandem palladium-catalyzed Heck and alkoxycarbonylation reactions	-
[夏克山] 期刊論文	2015-06-15	Synthesis and evaluation of 3-ylideneoxindole acetamides as potent anticancer agents	-
[葉燈光] 期刊論文	2013-11	BPR0C305, an orally active microtubule-disrupting anticancer agent	-
[趙宇生(2002-2013)] 期刊論文	2012-02	Synthesis and biological evaluation of 2-amino-1-thiazolyl imidazoles as orally active anticancer agents	-
[陳炯東] 期刊論文	2011-10	Antiproliferative effects of N-heterocyclic indolyl glyoxylamide derivatives on human lung cancer cells	-
[陳炯東] 期刊論文	2011-01	BPR0C261 is a novel orally active antitumor agent with antimitotic and anti-angiogenic activities	-
[陳炯東] 專利	2010-05-11	咪唑胺化合物	-
[陳炯東] 專利	2010-04-21	吲哚-3-基-2-氧乙醯胺衍生物之新化合物及其醫藥組合物與製備方法	-
[陳炯東] 期刊論文	2010-03	Synthesis and biological activities of 2-Amino-1-arylidenamino imidazoles as orally active anticancer agents	-
[陳淑貞(1998-2001)] 專利	2010-02-16	Methods of 1H-indol-3-yl-2-oxoacetamide compounds	-
[陳炯東] 專利	2009-08-04	Imidazolamino compounds	-
[陳炯東] 專利	2008-12-09	Imidazolamino compounds	-
[陳炯東] 專利	2008-07-08	Use of 1H-indol-3-yl-2-oxoacetamide compounds	-
[陳炯東] 專利	2006-09-19	Imidazolamino compounds	-
[趙宇生(2002-2013)] 期刊論文	2004-09	Mutation in enterovirus 71 capsid protein VP1 confers resistance to the inhibitory effects of pyridyl imidazolidinone	-
[夏克山] 專利	2004-06-01	咪唑啉酮化合物	-
[陳炯東] 期刊論文	2003-04-24	Synthesis and biological evaluation of N-heterocyclic indolyl glyoxylamides as orally active anticancer agents	-
[張仲明] 會議論文/會議摘要	2002-08	Design, synthesis, and structure-activity relationship of pyridyl imidazolidinones: A novel class of potent and selective human enterovirus 71 inhibitors	-
[陳志豪] 期刊論文	2002-04-11	Design, synthesis, and structure-activity relationship of pyridyl imidazolidinones: A novel class of potent and selective human enterovirus 71 inhibitors	-

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