| Literature DB >> 32980445 |
Yaiza Fernández-García1, Sebastiaan Ter Horst2, Marcella Bassetto3, Andrea Brancale4, Johan Neyts2, Dominga Rogolino5, Mario Sechi6, Mauro Carcelli5, Stephan Günther7, Joana Rocha-Pereira8.
Abstract
Several fatal bunyavirus infections lack specific treatment. Here, we show that diketo acids engage a panel of bunyavirus cap-snatching endonucleases, inhibit their catalytic activity and reduce viral replication of a taxonomic representative in vitro. Specifically, the non-salt form of L-742,001 and its derivatives exhibited EC50 values between 5.6 and 6.9 μM against a recombinant BUNV-mCherry virus. Structural analysis and molecular docking simulations identified traits of both the class of chemical entities and the viral target that could help the design of novel, more potent molecules for the development of pan-bunyavirus antivirals.Entities:
Keywords: Broad-spectrum antiviral; Bunyavirales; Cap-snatching endonuclease; Diketo acid; L-742,001; Metal chelators
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Year: 2020 PMID: 32980445 DOI: 10.1016/j.antiviral.2020.104947
Source DB: PubMed Journal: Antiviral Res ISSN: 0166-3542 Impact factor: 5.970