tetano
Editor, Senior Moderator
Antiviral Res. 2014 Apr 29. pii: S0166-3542(14)00119-3. doi: 10.1016/j.antiviral.2014.04.013. [Epub ahead of print]
Synthesis and anti-influenza virus activity of 4-oxo- or thioxo-4,5-dihydrofuro[3,4-c]pyridin-3(1H)-ones.
Jang YJ1, Achary R2, Lee HW1, Lee HJ3, Lee CK3, Han SB2, Jung YS2, Kang NS4, Kim P5, Kim M6.
Author information
Abstract
A target-free approach was applied to discover anti-influenza viral compounds, where influenza infected Madin-Darby canine kidney cells were treated 7,500 different small organic chemicals individually and reduction of virus-induced cytopathic effect was measured. One of the hit compounds was (Z)-1-((5-fluoro-1H-indol-3-yl)methylene)-6-methyl-4-thioxo-4,5-dihydrofuro[3,4-c]pyridin-3(1H)-one (15a) with half-maximal effective concentrations of 17.4-21.1 μM against influenza A/H1N1, A/H3N2 and B viruses without any cellular toxicity at 900 μM. To investigate the structure-activity relationships, two dozens of the hit analogs were synthesized. Among them, 15g, 15j, 15q, 15s, 15t and 15x had anti-influenza viral activity comparable or superior to that of the initial hit. The anti-influenza viral compounds efficiently suppressed not only viral protein level of the infected cells but also production of viral progeny in the culture supernatants in a dose-dependent manner. Based on a mode-of-action study, they did not affect virus entry or RNA replication. Instead, they suppressed viral neuraminidase activity. This study is the first to demonstrate that dihydrofuropyridinones could serve as lead compounds for the discovery of alternative influenza virus inhibitors.
Copyright ? 2014. Published by Elsevier B.V.
KEYWORDS:
Antiviral, Cytopathic reduction assay, Dihydrofuropyridinones, Influenza virus, NA inhibitor
PMID:
24794525
[PubMed - as supplied by publisher]
http://www.ncbi.nlm.nih.gov/pubmed/24794525
Synthesis and anti-influenza virus activity of 4-oxo- or thioxo-4,5-dihydrofuro[3,4-c]pyridin-3(1H)-ones.
Jang YJ1, Achary R2, Lee HW1, Lee HJ3, Lee CK3, Han SB2, Jung YS2, Kang NS4, Kim P5, Kim M6.
Author information
Abstract
A target-free approach was applied to discover anti-influenza viral compounds, where influenza infected Madin-Darby canine kidney cells were treated 7,500 different small organic chemicals individually and reduction of virus-induced cytopathic effect was measured. One of the hit compounds was (Z)-1-((5-fluoro-1H-indol-3-yl)methylene)-6-methyl-4-thioxo-4,5-dihydrofuro[3,4-c]pyridin-3(1H)-one (15a) with half-maximal effective concentrations of 17.4-21.1 μM against influenza A/H1N1, A/H3N2 and B viruses without any cellular toxicity at 900 μM. To investigate the structure-activity relationships, two dozens of the hit analogs were synthesized. Among them, 15g, 15j, 15q, 15s, 15t and 15x had anti-influenza viral activity comparable or superior to that of the initial hit. The anti-influenza viral compounds efficiently suppressed not only viral protein level of the infected cells but also production of viral progeny in the culture supernatants in a dose-dependent manner. Based on a mode-of-action study, they did not affect virus entry or RNA replication. Instead, they suppressed viral neuraminidase activity. This study is the first to demonstrate that dihydrofuropyridinones could serve as lead compounds for the discovery of alternative influenza virus inhibitors.
Copyright ? 2014. Published by Elsevier B.V.
KEYWORDS:
Antiviral, Cytopathic reduction assay, Dihydrofuropyridinones, Influenza virus, NA inhibitor
PMID:
24794525
[PubMed - as supplied by publisher]
http://www.ncbi.nlm.nih.gov/pubmed/24794525