Diana G D, Salvador U J, Zalay E S, Carabateas P M, Williams G L, Collins J C, Pancic F
J Med Chem. 1977 Jun;20(6):757-61. doi: 10.1021/jm00216a004.
A series of aryloxy alkyl diketones II was synthesized and screened in vitro for antiviral activity. The effect of various substituents on the phenyl ring, as well as the length of the alkyl bridge, was examined to establish the requirements for optimum activity. One of the most active members of the series, 4-[6-(2-chloro-4-methoxy)phenoxy]hexyl-3,5-heptanedione (56), exhibited a high level of activity against both DNA and RNA viruses in both the tissue culture and organ culture screens and was particularly effective against herpesvirus type 1 and 2.
合成了一系列芳氧基烷基二酮II,并对其进行了体外抗病毒活性筛选。研究了苯环上各种取代基以及烷基桥长度的影响,以确定最佳活性的要求。该系列中活性最高的成员之一,4-[6-(2-氯-4-甲氧基)苯氧基]己基-3,5-庚二酮(56),在组织培养和器官培养筛选中对DNA和RNA病毒均表现出高水平的活性,对1型和2型疱疹病毒尤其有效。