Computer-Aided Design, Synthesis, and Anti-HIV-1 Activity in Vitro of2-Alkylamino-6-[1-(2,6-difluorophenyl)alkyl]-3,4-dihydro-5-alkylpyrimidin-4(3H)-ones as Novel Potent Non-Nucleoside Reverse Transcriptase Inhibitors, AlsoActive Against the Y181C Variant

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	Computer-Aided Design, Synthesis, and Anti-HIV-1 Activity in Vitro of2-Alkylamino-6-[1-(2,6-difluorophenyl)alkyl]-3,4-dihydro-5-alkylpyrimidin-4(3H)-ones as Novel Potent Non-Nucleoside Reverse Transcriptase Inhibitors, AlsoActive Against the Y181C Variant
	JULIA A. KLEIN; JOHN HARTE; XIN-QUAN ZHAO
	2004
发表期刊	J. Med. Chem.
卷号	47 页码:928-934
语种	英语
文献类型	期刊论文
条目标识符	http://ir.kib.ac.cn/handle/151853/51969
专题	共享文献
推荐引用方式 GB/T 7714	JULIA A. KLEIN,JOHN HARTE,XIN-QUAN ZHAO. Computer-Aided Design, Synthesis, and Anti-HIV-1 Activity in Vitro of2-Alkylamino-6-[1-(2,6-difluorophenyl)alkyl]-3,4-dihydro-5-alkylpyrimidin-4(3H)-ones as Novel Potent Non-Nucleoside Reverse Transcriptase Inhibitors, AlsoActive Against the Y181C Variant[J]. J. Med. Chem.,2004,47:928-934.
APA	JULIA A. KLEIN,JOHN HARTE,&XIN-QUAN ZHAO.(2004).Computer-Aided Design, Synthesis, and Anti-HIV-1 Activity in Vitro of2-Alkylamino-6-[1-(2,6-difluorophenyl)alkyl]-3,4-dihydro-5-alkylpyrimidin-4(3H)-ones as Novel Potent Non-Nucleoside Reverse Transcriptase Inhibitors, AlsoActive Against the Y181C Variant.J. Med. Chem.,47,928-934.
MLA	JULIA A. KLEIN,et al."Computer-Aided Design, Synthesis, and Anti-HIV-1 Activity in Vitro of2-Alkylamino-6-[1-(2,6-difluorophenyl)alkyl]-3,4-dihydro-5-alkylpyrimidin-4(3H)-ones as Novel Potent Non-Nucleoside Reverse Transcriptase Inhibitors, AlsoActive Against the Y181C Variant".J. Med. Chem. 47(2004):928-934.