2013
DOI: 10.3390/ijms140817193
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Design, Synthesis and Antiviral Activity Studies of Schizonepetin Derivatives

Abstract: A series of schizonepetin derivatives have been designed and synthesized in order to obtain potent antivirus agents. The antiviral activity against HSV-1 and influenza virus H3N2 as well as the cytotoxicity of these derivatives was evaluated by using cytopathic effect (CPE) inhibition assay in vitro. Compounds M2, M4, M5 and M34 showed higher inhibitory activity against HSV-1 virus with the TC50 values being in micromole. Compounds M28, M33, and M35 showed higher inhibitory activity against influenza virus H3N… Show more

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Cited by 2 publications
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“…VZV-associated diseases can be effectively treated with nucleoside analogs such as acyclovir (ACV) and famciclovir, which inhibit viral DNA synthesis [7,9]. However, the effectiveness of these drugs to treat VZV infections in immunocompromised and in immunodeficient patients is limited due to the development of resistant VZV strains [7,10]. In addition, ACV and other available nucleoside analogs have different undesired side effects (like nausea, vomiting, headache and others) [11], and are not highly effective against reactivated herpes viruses [12,13].…”
Section: Introductionmentioning
confidence: 99%
“…VZV-associated diseases can be effectively treated with nucleoside analogs such as acyclovir (ACV) and famciclovir, which inhibit viral DNA synthesis [7,9]. However, the effectiveness of these drugs to treat VZV infections in immunocompromised and in immunodeficient patients is limited due to the development of resistant VZV strains [7,10]. In addition, ACV and other available nucleoside analogs have different undesired side effects (like nausea, vomiting, headache and others) [11], and are not highly effective against reactivated herpes viruses [12,13].…”
Section: Introductionmentioning
confidence: 99%
“…The latent virus is reactivated spontaneously causing recurrent infections in infected patients [6]. Although it can effectively be treated with nucleoside analogs such as acyclovir (ACV), but still the search for new effective antiherpetic drugs is important due to the development of ACV-resistant herpes viruses mutants particularly in immunosuppressed and in immunode iciency syndrome patients [7][8][9][10][11][12][13][14][15]. In addition, ACV and other available nucleoside analogs have different undesired side effects (like nausea, vomiting, headache and others) [16] and are not highly effective against reactivated herpes viruses [17,18].…”
Section: Introductionmentioning
confidence: 99%