Recent Progress in the Development of HIV-1 Protease Inhibitors for the Treatment of HIV/AIDS

AK Ghosh, HL Osswald, G Prato - Journal of medicinal chemistry, 2016 - ACS Publications
HIV-1 protease inhibitors continue to play an important role in the treatment of HIV/AIDS,
transforming this deadly ailment into a more manageable chronic infection. Over the years …

[HTML][HTML] Viral proteases as therapeutic targets

T Majerová, J Konvalinka - Molecular aspects of medicine, 2022 - Elsevier
Some medically important viruses―including retroviruses, flaviviruses, coronaviruses, and
herpesviruses―code for a protease, which is indispensable for viral maturation and …

The anti‐HIV drug nelfinavir mesylate (Viracept) is a potent inhibitor of cell fusion caused by the SARSCoV‐2 spike (S) glycoprotein warranting further evaluation as …

F Musarrat, V Chouljenko, A Dahal… - Journal of medical …, 2020 - Wiley Online Library
Severe acute respiratory syndrome coronavirus‐2 (SARS CoV‐2) is the causative agent of
the coronavirus disease‐2019 (COVID‐19) pandemic. Coronaviruses enter cells via fusion …

HIV-1 protease: structural perspectives on drug resistance

IT Weber, J Agniswamy - Viruses, 2009 - pmc.ncbi.nlm.nih.gov
Antiviral inhibitors of HIV-1 protease are a notable success of structure-based drug design
and have dramatically improved AIDS therapy. Analysis of the structures and activities of …

Systematic analyses of the resistance potential of drugs targeting SARS-CoV-2 main protease

JM Flynn, QYJ Huang, SN Zvornicanin… - ACS infectious …, 2023 - ACS Publications
Drugs that target the main protease (Mpro) of SARS-CoV-2 are effective therapeutics that
have entered clinical use. Wide-scale use of these drugs will apply selection pressure for the …

A reliable docking/scoring scheme based on the semiempirical quantum mechanical PM6-DH2 method accurately covering dispersion and H-bonding: HIV-1 protease …

J Fanfrlik, AK Bronowska, J Rezac… - The Journal of …, 2010 - ACS Publications
In this study, we introduce a fast and reliable rescoring scheme for docked complexes based
on a semiempirical quantum mechanical PM6-DH2 method. The method utilizes a PM6 …

Current and novel inhibitors of HIV protease

J Pokorná, L Machala, P Řezáčová, J Konvalinka - Viruses, 2009 - mdpi.com
The design, development and clinical success of HIV protease inhibitors represent one of
the most remarkable achievements of molecular medicine. This review describes all nine …

Catalytic contributions from remote regions of enzyme structure

J Lee, NM Goodey - Chemical reviews, 2011 - ACS Publications
Although many protein variants have properties similar to their corresponding wild-type
structures, the replacement of a single amino acid often produces dramatic changes in …

Amino Acid and Peptide‐Based Antiviral Agents

AS Skwarecki, MG Nowak, MJ Milewska - ChemMedChem, 2021 - Wiley Online Library
A significant number of antiviral agents used in clinical practice are amino acids, short
peptides, or peptidomimetics. Among them, several HIV protease inhibitors (eg lopinavir …

HIV-1 protease with 20 mutations exhibits extreme resistance to clinical inhibitors through coordinated structural rearrangements

J Agniswamy, CH Shen, A Aniana, JM Sayer… - Biochemistry, 2012 - ACS Publications
The escape mutant of HIV-1 protease (PR) containing 20 mutations (PR20) undergoes
efficient polyprotein processing even in the presence of clinical protease inhibitors (PIs) …