The evolution of antiviral nucleoside analogues: A review for chemists and non-chemists. Part II: Complex modifications to the nucleoside scaffold

MK Yates, KL Seley-Radtke - Antiviral research, 2019 - Elsevier
This is the second of two invited articles reviewing the development of nucleoside analogue
antiviral drugs, written for a target audience of virologists and other non-chemists, as well as …

4′-Modified nucleosides for antiviral drug discovery: achievements and perspectives

J Chang - Accounts of Chemical Research, 2022 - ACS Publications
Conspectus Modified nucleosides show therapeutic promise for antiviral therapies.
However, issues including the emergence of drug resistance, toxicity, and coinfections have …

Avoiding drug resistance in HIV reverse transcriptase

ME Cilento, KA Kirby, SG Sarafianos - Chemical reviews, 2021 - ACS Publications
HIV reverse transcriptase (RT) is an enzyme that plays a major role in the replication cycle of
HIV and has been a key target of anti-HIV drug development efforts. Because of the high …

HIV nucleoside reverse transcriptase inhibitors

F Amblard, D Patel, E Michailidis, SJ Coats… - European journal of …, 2022 - Elsevier
More than 40 years into the pandemic, HIV remains a global burden and as of now, there is
no cure in sight. Fortunately, highly active antiretroviral therapy (HAART) has been …

HIV‐1 reverse transcriptase still remains a new drug target: structure, function, classical inhibitors, and new inhibitors with innovative mechanisms of actions

F Esposito, A Corona… - Molecular biology …, 2012 - Wiley Online Library
During the retrotranscription process, characteristic of all retroviruses, the viral ssRNA
genome is converted into integration‐competent dsDNA. This process is accomplished by …

Islatravir has a high barrier to resistance and exhibits a differentiated resistance profile from approved nucleoside reverse transcriptase inhibitors (NRTIs)

TL Diamond, W Ngo, M Xu, SL Goh… - Antimicrobial Agents …, 2022 - Am Soc Microbiol
Islatravir (ISL) is a nucleoside reverse transcriptase translocation inhibitor (NRTTI) that
inhibits human immunodeficiency virus (HIV) reverse transcription by blocking reverse …

Studies on in vitro antioxidant and antistaphylococcal activities of some important medicinal plants

A Mishra, S Kumar, A Bhargava… - Cellular and …, 2011 - mail.cellmolbiol.org
Oxidative stress is initiated by free radicals, which seek stability through electron pairing with
biological macromolecules in healthy human cells and cause protein and DNA damage …

Recent Advances in Molecular Mechanisms of Nucleoside Antivirals

PN Kamzeeva, AV Aralov, VA Alferova… - Current Issues in …, 2023 - mdpi.com
The search for new drugs has been greatly accelerated by the emergence of new viruses
and drug-resistant strains of known pathogens. Nucleoside analogues (NAs) are a …

Structure, Synthesis and Inhibition Mechanism of Nucleoside Analogues as HIV‐1 Reverse Transcriptase Inhibitors (NRTIs)

Y Yoshida, M Honma, Y Kimura, H Abe - ChemMedChem, 2021 - Wiley Online Library
Acquired immunodeficiency syndrome (AIDS) is caused by infection with the human
immunodeficiency virus (HIV). Although treatments against HIV infection are available, AIDS …

Development of human immunodeficiency virus type 1 resistance to 4′-ethynyl-2-fluoro-2′-deoxyadenosine starting with wild-type or nucleoside reverse …

ME Cilento, AB Reeve, E Michailidis… - Antimicrobial Agents …, 2021 - Am Soc Microbiol
Ethynyl-2-fluoro-2′-deoxyadenosine (EFdA, MK-8591, islatravir) is a nucleoside reverse
transcriptase translocation inhibitor (NRTTI) with exceptional potency against wild-type (WT) …