出处
《北京大学学报(医学版)》
CAS
CSCD
北大核心
2005年第5期560-560,F0003,共2页
Journal of Peking University:Health Sciences
基金
国家自然科学基金(20172007)资助~~
参考文献7
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同被引文献7
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1Chen, Y. L.; Guo, Y.; Yang, H.; Wang, X. W.; Liu, J. Y. Synth. Commun. 2006, 36, 2913.
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2Wang, X. W.; Lou, Q. H.; Guo, Y.; Xu, Y.; Zhang, Z. L.; Liu, J. Y. Org. Biomol. Chem. 2006, 4, 3252.
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7韩鹏,王孝伟,张志丽,陈林丽,刘俊义.蛋氨酸合成酶催化反应研究 VII.5-氨基-6-甲基尿嘧啶的合成研究[J].有机化学,2003,23(10):1111-1113. 被引量:1
引证文献1
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1马小艳,王瑞平,李阿敏,陈艳丽,王孝伟,张志丽,刘俊义.1,3-二(乙氧基甲基)-5-N,N-二甲氨基-6-甲基尿嘧啶的合成[J].有机化学,2008,28(2):301-303. 被引量:1
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1赵培亮,游文玮,段安娜.具有抗肿瘤活性的嘧啶类化合物研究进展[J].药学学报,2012,47(5):580-587. 被引量:7
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2姜楠,李婷,陶海燕,宫平.2-取代-4-氨基噻吩并[3,2-d]嘧啶类化合物的合成及抗增殖活性[J].沈阳药科大学学报,2012,29(11):829-833. 被引量:1
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3孟歌,陈芬儿.HEPT类HIV-1逆转录酶抑制剂的研究进展[J].中国药物化学杂志,2004,14(1):56-64. 被引量:12
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4闫寒,王孝伟,郭盈,张志丽,刘俊义.Synthesis and anti-HIV-1 activity evaluation of N-1-alkyl-5-halogeno-6-alkylamino uracils as novel non-nucleoside HIV-1 reverse transcriptase inhibitors[J].Journal of Chinese Pharmaceutical Sciences,2011,20(2X):146-153.
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5许莉,黄一玲,华潞,田蕾,李飞鸥,况扶华,李一石.重组人组织型纤溶酶原激活剂TNK突变体在中国健康人体的耐受性及药代动力学研究[J].中国临床药理学杂志,2015,31(9):734-737. 被引量:10
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6杨秀岩,赵国明,李松.以乙肝病毒核衣壳为靶标的二氢嘧啶类化合物及其作用机制研究进展[J].中国药物化学杂志,2013,23(6):493-498. 被引量:1
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7周原,梅虎,梁桂兆,杨善彬,李志良.取代基物化参数用于HEPT类HIV-1逆转录酶抑制剂的QSAR研究[J].精细化工,2006,23(9):907-911. 被引量:2
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8何严萍,胡海荣,许辽萨,孟歌,范康年,陈芬儿.基于分子对接的6-萘甲基取代HEPT类HIV-1逆转录酶抑制剂构效关系研究[J].高等学校化学学报,2005,26(2):254-258. 被引量:8
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9刘斌,左斌海,孙超,蔡泽江,鄢明.三唑并[4,5-d]嘧啶类化合物的合成及其抗血小板聚集活性研究[J].中国药物化学杂志,2015,25(1):1-7. 被引量:1
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10董铭心,赵国明,李松.抗乙型肝炎病毒药物的研究进展[J].国外医学(药学分册),2004,31(5):296-299. 被引量:3