Abstract |
In this study we report the design, synthesis, and activity against bovine viral diarrhea virus (BVDV) of a novel series of acridone derivatives. BVDV is responsible for major losses in cattle. The virus is also considered to be a valuable surrogate for the hepatitis C virus (HCV) in antiviral drug studies. Some of the synthesized acridones elicited selective anti-BVDV activity with EC(50) values ranging from 0.4 to 4 microg/mL and were not cytotoxic at concentrations that were 25- to 200-fold higher (CC(50) >100 microg/mL). It was proven that the most potent acridone derivative 10 was able to not only protect cells from virus-induced cytopathic effect but also reduce the production of infectious virus and extracellular viral RNA. Furthermore, compound 10, as well as a number of other analogues, inhibited HCV replication to some extent. However, there was no direct correlation between anti-BVDV and anti-HCV activity. Thus, the acridone scaffold, when appropriately functionalized, can yield compounds with selective activity against pestiviruses and related viruses such as the HCV.
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Authors | Oriana Tabarrini, Giuseppe Manfroni, Arnaldo Fravolini, Violetta Cecchetti, Stefano Sabatini, Erik De Clercq, Jef Rozenski, Bruno Canard, Hélène Dutartre, Jan Paeshuyse, Johan Neyts |
Journal | Journal of medicinal chemistry
(J Med Chem)
Vol. 49
Issue 8
Pg. 2621-7
(Apr 20 2006)
ISSN: 0022-2623 [Print] United States |
PMID | 16610805
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Acridines
- Acridones
- Antiviral Agents
- acridone
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Topics |
- Acridines
(chemical synthesis, chemistry, pharmacology)
- Acridones
- Animals
- Antiviral Agents
(chemical synthesis, chemistry, pharmacology)
- Binding Sites
- Cattle
- Cell Proliferation
(drug effects)
- Diarrhea Viruses, Bovine Viral
(drug effects)
- Drug Design
- Kidney
(cytology, drug effects)
- Microbial Sensitivity Tests
- Molecular Structure
- Structure-Activity Relationship
- Virus Replication
(drug effects)
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