Propellanes—from a chemical curiosity to “explosive” materials and natural products

AM Dilmaç, E Spuling, A de Meijere… - Angewandte Chemie …, 2017 - Wiley Online Library
Propellanes are a unique class of compounds currently consisting of well over 10 000
representatives, all featuring two more or less inverted tetrahedral carbon atoms that are …

Viroporins: structure, function and potential as antiviral targets

C Scott, S Griffin - Journal of General Virology, 2015 - microbiologyresearch.org
The channel-forming activity of a family of small, hydrophobic integral membrane proteins
termed 'viroporins' is essential to the life cycles of an increasingly diverse range of RNA and …

Inhibition of H1N1 influenza virus-induced apoptosis by functionalized selenium nanoparticles with amantadine through ROS-mediated AKT signaling pathways

Y Li, Z Lin, M Guo, M Zhao, Y Xia, C Wang… - International journal …, 2018 - Taylor & Francis
Introduction As a therapeutic antiviral agent, the clinical application of amantadine (AM) is
limited by the emergence of drug-resistant viruses. To overcome the drug-resistant viruses …

Put a cork in it: Plugging the M2 viral ion channel to sink influenza

PH Jalily, MC Duncan, D Fedida, J Wang, I Tietjen - Antiviral research, 2020 - Elsevier
The ongoing threat of seasonal and pandemic influenza to human health requires antivirals
that can effectively supplement existing vaccination strategies. The M2 protein of influenza A …

Inhibitors of influenza virus polymerase acidic (PA) endonuclease: contemporary developments and perspectives

H Ju, J Zhang, B Huang, D Kang, B Huang… - Journal of Medicinal …, 2017 - ACS Publications
Influenza virus (IFV) causes periodic global influenza pandemics, resulting in substantial
socioeconomic loss and burden on medical facilities. Yearly variation in the effectiveness of …

Heterocyclic inhibitors of viroporins in the design of antiviral compounds

VA Shiryaev, YN Klimochkin - Chemistry of heterocyclic compounds, 2020 - Springer
Ion channels of viruses (viroporins) represent a common type of protein targets for drugs.
The relative simplicity of channel architecture allows convenient computational modeling …

Reversal of H1N1 influenza virus-induced apoptosis by silver nanoparticles functionalized with amantadine

Y Li, Z Lin, M Zhao, M Guo, T Xu, C Wang, H Xia… - RSC advances, 2016 - pubs.rsc.org
Amantadine is an antiviral agent, but its clinical use against influenza viruses is limited
because of the emergence of drug-resistant viruses. Thus, there is a need for novel anti …

Recent progress in designing inhibitors that target the drug‐resistant M2 proton channels from the influenza A viruses

J Wang, F Li, C Ma - Peptide Science, 2015 - Wiley Online Library
Influenza viruses are the causative agents for seasonal influenza, which results in
thousands of deaths and millions of hospitalizations each year. Moreover, sporadic …

X-ray crystal structures of the influenza M2 proton channel drug-resistant V27A mutant bound to a spiro-adamantyl amine inhibitor reveal the mechanism of …

JL Thomaston, A Konstantinidi, L Liu, G Lambrinidis… - Biochemistry, 2020 - ACS Publications
The V27A mutation confers adamantane resistance on the influenza A matrix 2 (M2) proton
channel and is becoming more prevalent in circulating populations of influenza A virus. We …

[HTML][HTML] Real-time tracking of drug binding to influenza A M2 reveals a high energy barrier

KT Movellan, M Wegstroth, K Overkamp… - Journal of Structural …, 2023 - Elsevier
The drug Rimantadine binds to two different sites in the M2 protein from influenza A, a
peripheral site and a pore site that is the primary site of efficacy. It remained enigmatic that …