作为潜在抗HIV药物的取代喹唑啉酮衍生物的合成（第三部分）。
Synthesis of substituted quinazolone derivatives as potential anti-HIV agents (Part III).
作者信息
Desai N C, Bhatt J J, Shah B R, Undavia N K, Trivedi P B, Narayanan V
机构信息
Department of Chemistry, Bhavnagar University, India.
出版信息
Farmaco. 1996 May;51(5):361-6.
PMID:8767846
Abstract
Several 1-[2-phenyl-4(4H)-oxo-3-quinazolinyl]-2-methyl-4-arylidine -5-oxo-imidazolines (Va-1), 2-phenyl-3-(aroyl amino)-4(4H)-oxo quinazolines (Vla-I) and N1-2-methyl-4(4H)-oxo-3-quinazolinyl-N2-aryl-thioureas (Vlla-k), have been synthesised and tested for anti-HIV activity. The structures of these compounds have been established on the basis of elemental analysis and spectral data.
摘要
合成了几种1-[2-苯基-4(4H)-氧代-3-喹唑啉基]-2-甲基-4-芳叉基-5-氧代-咪唑啉（Va-1）、2-苯基-3-(芳酰基氨基)-4(4H)-氧代喹唑啉（Vla-I）和N1-2-甲基-4(4H)-氧代-3-喹唑啉基-N2-芳基硫脲（Vlla-k），并对其抗HIV活性进行了测试。这些化合物的结构已通过元素分析和光谱数据确定。
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