Medicinal chemistry strategies for discovering antivirals effective against drug-resistant viruses

Y Ma, E Frutos-Beltrán, D Kang… - Chemical Society …, 2021 - pubs.rsc.org
During the last forty years we have witnessed impressive advances in the field of antiviral
drug discovery culminating with the introduction of therapies able to stop human …

Advances in respiratory virus therapeutics–A meeting report from the 6th isirv Antiviral Group conference

JH Beigel, HH Nam, PL Adams, A Krafft, WL Ince… - Antiviral research, 2019 - Elsevier
Abstract The International Society for Influenza and other Respiratory Virus Diseases held its
6th Antiviral Group (isirv-AVG) conference in Rockville, Maryland, November 13–15, 2018 …

Overview of recent strategic advances in medicinal chemistry

G Wu, T Zhao, D Kang, J Zhang, Y Song… - Journal of medicinal …, 2019 - ACS Publications
Introducing novel strategies, concepts, and technologies that speed up drug discovery and
the drug development cycle is of great importance both in the highly competitive …

Targeting ribonucleases with small molecules and bifunctional molecules

L Borgelt, P Wu - ACS Chemical Biology, 2023 - ACS Publications
Ribonucleases (RNases) cleave and process RNAs, thereby regulating the biogenesis,
metabolism, and degradation of coding and noncoding RNAs. Thus, small molecules …

Baloxavir marboxil: an original new drug against influenza

F Dufrasne - Pharmaceuticals, 2021 - mdpi.com
Baloxavir marboxil is a new drug developed in Japan by Shionogi to treat seasonal flu
infection. This cap-dependent endonuclease inhibitor is a prodrug that releases the …

Interplay between influenza virus and the host RNA polymerase II transcriptional machinery

AP Walker, E Fodor - Trends in microbiology, 2019 - cell.com
The influenza virus RNA-dependent RNA polymerase (RdRP) cleaves the 5′ end of
nascent capped host RNAs and uses the capped RNA fragment to prime viral transcription …

Design, synthesis and anti-influenza A virus activity of novel 2, 4-disubstituted quinazoline derivatives

M Wang, G Zhang, Y Wang, J Wang, M Zhu… - Bioorganic & Medicinal …, 2020 - Elsevier
Abstract Four 2, 4-disubstituted quinazoline series containing various amide moieties were
designed and synthesized as new anti-influenza A virus agents using the strategies of bio …

Rational design and optimization of acylthioureas as novel potent influenza virus non-nucleoside polymerase inhibitors

X Liu, Z Xu, J Liang, T Xu, W Zou, L Zhu, Y Wu… - European Journal of …, 2023 - Elsevier
Evidence suggests that rapidly evolving virus subvariants risk rendering current vaccines
and anti-influenza drugs ineffective. Hence, exploring novel scaffolds or new targets of anti …

Identification of N- and C-3-Modified Laudanosoline Derivatives as Novel Influenza PAN Endonuclease Inhibitors

Y Liao, Y Ye, M Liu, Z Liu, J Wang, B Li… - Journal of Medicinal …, 2022 - ACS Publications
Influenza PAN inhibitors are of particular importance in current efforts to develop a new
generation of antiviral drugs due to the growing emergence of highly pathogenic influenza …

Synthesis and antiviral activity of a series of novel quinoline derivatives as anti-RSV or anti-IAV agents

M Wang, G Zhang, J Zhao, N Cheng, Y Wang… - European Journal of …, 2021 - Elsevier
We report herein the synthesis of a series of novel quinoline derivatives, based on the lead
compound 1a, identified from a rRSV-mGFP high-throughput screening assay. Our results …