[HTML][HTML] Design of inhibitors of SARS-CoV-2 papain-like protease deriving from GRL0617: Structure–activity relationships

L Kerti, V Frecer - Bioorganic & Medicinal Chemistry, 2024 - Elsevier
The unique and complex structure of papain-like protease (PL pro) of the SARS-CoV-2 virus
represents a difficult challenge for antiviral development, yet it offers a compelling validated …

Small Molecule Drugs Targeting Viral Polymerases

D Palazzotti, M Sguilla, G Manfroni, V Cecchetti… - Pharmaceuticals, 2024 - mdpi.com
Small molecules that specifically target viral polymerases—crucial enzymes governing viral
genome transcription and replication—play a pivotal role in combating viral infections …

σ-Hole Site-Based Interactions within Hypervalent Pnicogen, Halogen, and Aerogen-Bearing Molecules with Lewis Bases: A Comparative Study

MAA Ibrahim, AMM Mahmoud, MNI Shehata… - ACS …, 2024 - ACS Publications
σ-Hole site-based interactions in the trigonal bipyramidal geometrical structure of
hypervalent pnicogen, halogen, and aerogen-bearing molecules with pyridine and NCH …

On the Versatility of the sp-, sp2-, and sp3-Hybridized Chalcogen-Bearing Molecules To Engage in Type I Chalcogen···Chalcogen Interactions: A Quantum …

MAA Ibrahim, RRA Saeed, MNI Shehata… - ACS …, 2024 - ACS Publications
The predilection of sp-, sp 2-, and sp 3-hybridized chalcogen-bearing molecules to engage
in type I chalcogen··· chalcogen interactions was comparatively unveiled in like··· like/unlike …

Exploring nucleoside analogs: key targets in the viral life cycle-advancing strategies against SARS-CoV-2

R Garg, R Kumar, R Srivastava… - Medicinal Chemistry …, 2024 - Springer
The COVID-19 pandemic has been a major reason behind the increased research aimed at
the identification of effective antiviral agents. Among these, Nucleoside analogs have shown …

Molecular Mechanism of Molnupiravir-Induced Sars-Cov-2 Rna Mutagenesis: A Comparative Analysis with Cytosine

S De, G Sabu - Available at SSRN 4945375 - papers.ssrn.com
Nucleoside analogues (NAs) are recognized for its ability to impede viral RNA replication
through either chain termination or mutagenesis mechanism. Molnupiravir, an oral antiviral …