2003
DOI: 10.1016/s0166-3542(03)00106-2
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Cell culture replication of herpes simplex virus and, or human cytomegalovirus is inhibited by 3,7-dialkoxylated, 1-hydroxyacridone derivatives

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Cited by 30 publications
(13 citation statements)
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“…As for the antiviral properties of this class of compounds, several studies have shown the inhibitory action of acridone derivatives against DNA viruses such as herpes simplex virus and cytomegalovirus [45,46], Epstein-Barr virus [47] and adenovirus [48], as well as RNA viruses, including human immunodeficiency virus [49,50], bovine viral diarrhea virus [51] and hepatitis C [52,53]. The precise target and the mode of action of antiviral acridones are not clearly determined at present, although its predominant action seems to be centered on the synthesis of nucleic acids.…”
Section: Cellular Proteins Involved In Rna Synthesis or Processingmentioning
confidence: 99%
“…As for the antiviral properties of this class of compounds, several studies have shown the inhibitory action of acridone derivatives against DNA viruses such as herpes simplex virus and cytomegalovirus [45,46], Epstein-Barr virus [47] and adenovirus [48], as well as RNA viruses, including human immunodeficiency virus [49,50], bovine viral diarrhea virus [51] and hepatitis C [52,53]. The precise target and the mode of action of antiviral acridones are not clearly determined at present, although its predominant action seems to be centered on the synthesis of nucleic acids.…”
Section: Cellular Proteins Involved In Rna Synthesis or Processingmentioning
confidence: 99%
“…Published literature on natural and synthetic antiviral compounds reveals that the activity against HSV was often dependent on m.o.i. (Akanitapichat et al, 2000;del Barrio & Parra, 2000;Lowden & Bastow, 2003) and/or origin of host cell (Serkedjieva & Ivancheva, 1999;del Barrio & Parra, 2000). The current results indicated that inhibition of PPRV by BExt was much greater with lower (0.01) m.o.i.…”
Section: Resultsmentioning
confidence: 63%
“…Published work with natural and synthetic compounds showed that activity against HSV is often dependent on multiplicity of infection (Akanitapichat et al, 2000;del Barrio and Parra, 2000;Lowden and Bastow, 2003) and/or host cell (del Barrio and Parra, 2000;Serkedjieva and Ivancheva, 1999). We observed that HSV inhibition of Fr.372 in condition of low virus load was much greater than in high multiplicity infection.…”
Section: Discussionmentioning
confidence: 65%