Antiviral activity of some beta-diketones. 2. Aryloxy alkyl diketones. In vitro activity against both RNA and DNA viruses
Autor: | Guy D. Diana, U. Joseph Salvador, Ethel S. Zalay, Philip M. Carabateas, Gordon L. Williams, Joseph C. Collins, Francis Pancic |
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Rok vydání: | 1977 |
Předmět: |
chemistry.chemical_classification
Stereochemistry Chemistry DNA Viruses RNA Picornaviridae Ketones Organ culture Antiviral Agents In vitro chemistry.chemical_compound Tissue culture Structure-Activity Relationship Organ Culture Techniques Culture Techniques Drug Discovery Molecular Medicine Structure–activity relationship RNA Viruses Simplexvirus Beta (finance) Alkyl DNA |
Zdroj: | Journal of medicinal chemistry. 20(6) |
ISSN: | 0022-2623 |
Popis: | 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. |
Databáze: | OpenAIRE |
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