Main and papain-like proteases as prospective targets for pharmacological treatment of coronavirus SARS-CoV-2

LV Yevsieieva, KO Lohachova, A Kyrychenko… - RSC …, 2023 - pubs.rsc.org
The pandemic caused by the coronavirus SARS-CoV-2 led to a global crisis in the world
healthcare system. Despite some progress in the creation of antiviral vaccines and mass …

[HTML][HTML] Exploring the structural and molecular interaction landscape of nirmatrelvir and Mpro complex: The study might assist in designing more potent antivirals …

C Chakraborty, M Bhattacharya, A Alshammari… - Journal of Infection and …, 2023 - Elsevier
Background Several therapeutics have been developed and approved against SARS-CoV-2
occasionally; nirmatrelvir is one of them. The drug target of nirmatrelvir is Mpro, and …

Preclinical discovery and development of nirmatrelvir/ritonavir combinational therapy for the treatment of COVID-19 and the lessons learned from SARS-COV-2 …

P Pagliano, A Spera, C Sellitto, G Scarpati… - Expert Opinion on …, 2023 - Taylor & Francis
ABSTRACT Introduction Nirmatrelvir/ritonavir (Paxlovid®) represent an oral antiviral therapy
approved for the treatment of COVID-19. Extensive in vitro and in vivo studies have reported …

Acenocoumarol, an anticoagulant drug, prevents melanogenesis in B16F10 melanoma cells

H Han, C Hyun - Pharmaceuticals, 2023 - mdpi.com
Hyperpigmentation can occur in abnormal skin conditions such as melanomas, as well as in
conditions including melasma, freckles, age spots, seborrheic keratosis, and café-au-lait …

Characterization of a mouse-adapted strain of bat severe acute respiratory syndrome-related coronavirus

HF Lin, MQ Liu, RD Jiang, QC Gong, J Su… - Journal of …, 2023 - Am Soc Microbiol
Bats carry genetically diverse severe acute respiratory syndrome-related coronaviruses
(SARSr-CoVs). Some of them utilize human angiotensin-converting enzyme 2 (hACE2) as a …

Computer-aided drug design of novel nirmatrelvir analogs inhibiting main protease of Coronavirus SARS-CoV-2

KO Lohachova, AS Sviatenko… - Journal of Applied …, 2024 - japsonline.com
A computer-aided drug design of new derivatives of nirmatrelvir, an orally active inhibitor of
the main-protease (Mpro) of the severe acute respiratory syndrome Coronavirus 2 (SARS …

Benzene with Alkyl Chains Is a Universal Scaffold for Multivalent Virucidal Antivirals

Y Zhu, M Gasbarri, S Zebret, S Pawar… - ACS Central …, 2024 - ACS Publications
Most viruses start their invasion by binding to glycoproteins' moieties on the cell surface
(heparan sulfate proteoglycans [HSPG] or sialic acid [SA]). Antivirals mimicking these …

A low-background, fluorescent assay to evaluate inhibitors of diverse viral proteases

RA Leonard, VN Rao, A Bartlett, HM Froggatt… - Journal of …, 2023 - Am Soc Microbiol
Multiple coronaviruses (CoVs) can cause respiratory diseases in humans. While
prophylactic vaccines designed to prevent infection are available for severe acute …

[HTML][HTML] Broad-spectrum antiviral activity of two structurally analogous CYP3A inhibitors against pathogenic human coronaviruses in vitro

L Gallucci, J Bazire, AD Davidson, IL Shytaj - Antiviral Research, 2024 - Elsevier
Coronaviruses pose a permanent risk of outbreaks, with three highly pathogenic species
and strains (SARS-CoV, MERS-CoV, SARS-CoV-2) having emerged in the last twenty years …

Seasonal human coronaviruses OC43, 229E, and NL63 induce cell surface modulation of entry receptors and display host cell-specific viral replication kinetics

V Siragam, M Maltseva, N Castonguay… - Microbiology …, 2024 - Am Soc Microbiol
The emergence of the COVID-19 pandemic prompted an increased interest in seasonal
human coronaviruses. OC43, 229E, NL63, and HKU1 are endemic seasonal coronaviruses …