| Literature DB >> 195055 |
G D Diana, U J Salvador, E S Zalay, P M Carabateas, G L Williams, J C Collins, F Pancic.
Abstract
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.Entities:
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Year: 1977 PMID: 195055 DOI: 10.1021/jm00216a004
Source DB: PubMed Journal: J Med Chem ISSN: 0022-2623 Impact factor: 7.446