Glycopeptides, a class of cell wall biosynthesis inhibitors, have been the antibiotics of choice
against drug-resistant Gram-positive bacterial infections. Their unique mechanism of action …

Influenza A and B viruses are highly contagious respiratory pathogens with a considerable
medical and socioeconomical burden and known pandemic potential. Current influenza …

ABSTRACT A new class of N-(1-thia-4-azaspiro [4.5] decan-4-yl) carboxamide inhibitors of
influenza virus hemagglutinin (HA)-mediated membrane fusion that has a narrow and …

This review is the sixth update of the original article published in 1999 on the application of
MALDI mass spectrometry to the analysis of carbohydrates and glycoconjugates and brings …

The vancomycin family of glycopeptide antibiotics has been inspiring research in the field of
synthetic chemistry since the 1980s. Recent studies have moved away from the focus of total …

A novel series of indolylthiosemicarbazides (6a–6g) and their cyclization products, 4-
thiazolidinones (7a–7g), have been designed, synthesized and evaluated, in vitro, for their …

In this work, novel 5-fluoro-1-methyl/ethyl-1H-indole-2, 3-dione 3-[4-(substituted phenyl)-
thiosemicarbazones] 6a-n and 7a-n were synthesized. The antiviral effects of the …

This review highlights ten “hot topics” in current antiviral research:(i) new nucleoside
derivatives (ie, PSI‐352938) showing high potential as a direct antiviral against hepatitis C …

The possible resistance of influenza virus against existing antiviral drugs calls for new
therapeutic concepts. One appealing strategy is to inhibit virus entry, in particular at the …

Patients infected with SARS-CoV-2 risk co-infection with Gram-positive bacteria, which
severely affects their prognosis. Antimicrobial drugs with dual antiviral and antibacterial …