Sialidase inhibitors with different mechanisms

JM Keil, GR Rafn, IM Turan, MA Aljohani… - Journal of medicinal …, 2022 - ACS Publications
Sialidases, or neuraminidases, are enzymes that catalyze the hydrolysis of sialic acid (Sia)-
containing molecules, mostly removal of the terminal Sia (desialylation). By desialylation …

[HTML][HTML] Antiviral strategies against influenza virus: towards new therapeutic approaches

A Loregian, B Mercorelli, G Nannetti… - Cellular and molecular …, 2014 - Springer
Influenza viruses are major human pathogens responsible for respiratory diseases affecting
millions of people worldwide and characterized by high morbidity and significant mortality …

Glycyrrhizic acid-based carbonized dots boost antiviral activity against influenza A virus via multisite inhibition mechanisms

C Li, P Han, H Mao, C Lv, K Huang… - ACS Applied Materials & …, 2023 - ACS Publications
Influenza A virus (IVA) has been continuously causing pandemics in several animal hosts
and has become a worldwide public health threat. Currently, antiviral drugs have become …

X-ray crystallography over the past decade for novel drug discovery–where are we heading next?

H Zheng, KB Handing, MD Zimmerman… - Expert opinion on …, 2015 - Taylor & Francis
Introduction: Macromolecular X-ray crystallography has been the primary methodology for
determining the three-dimensional structures of proteins, nucleic acids and viruses …

The chemistry and biology of guanidine natural products

RGS Berlinck, S Romminger - Natural Product Reports, 2016 - pubs.rsc.org
Covering: 2012 to 2014. Previous review: Nat. Prod. Rep., 2012, 29, 1382 The present
review discusses the isolation, structure determination, synthesis, biosynthesis and …

The future of crystallography in drug discovery

H Zheng, J Hou, MD Zimmerman… - Expert opinion on …, 2014 - Taylor & Francis
Introduction: X-ray crystallography plays an important role in structure-based drug design
(SBDD), and accurate analysis of crystal structures of target macromolecules and …

[HTML][HTML] Influenza neuraminidase inhibitors: synthetic approaches, derivatives and biological activity

P Laborda, SY Wang, J Voglmeir - Molecules, 2016 - mdpi.com
Despite being a common viral disease, influenza has very negative consequences, causing
the death of around half a million people each year. A neuraminidase located on the surface …

[HTML][HTML] Inhibition of Influenza A virus propagation by benzoselenoxanthenes stabilizing TMPRSS2 Gene G-quadruplex and hence down-regulating TMPRSS2 …

LW Shen, MQ Qian, K Yu, S Narva, F Yu, YL Wu… - Scientific Reports, 2020 - nature.com
Proteolytic cleavage of influenza A virus (IAV) hemagglutinin by host proteases is crucial for
virus infectivity and spread. The transmembrane serine protease TMPRSS2 was previously …

[HTML][HTML] New small-molecule drug design strategies for fighting resistant influenza A

Z Shen, K Lou, W Wang - Acta Pharmaceutica Sinica B, 2015 - Elsevier
Influenza A virus is the major cause of seasonal or pandemic flu worldwide. Two main
treatment strategies–vaccination and small molecule anti-influenza drugs are currently …

Influenza treatment and prophylaxis with neuraminidase inhibitors: a review

A Kamali, M Holodniy - Infection and drug resistance, 2013 - Taylor & Francis
Influenza virus is a pathogen that causes morbidity and mortality worldwide. Whereas
vaccination is important for prevention of disease, given its limitations, antiviral therapy is at …