Non-nucleoside reverse transcriptase inhibitors (NNRTIs): A brief overview of clinically approved drugs and combination regimens

M Vanangamudi, S Kurup, V Namasivayam - Current opinion in …, 2020 - Elsevier
The non-nucleoside reverse transcriptase inhibitors (NNRTIs) are allosteric inhibitors of HIV-
1 reverse transcriptase and are classified into generations depending on their discovery and …

Novel HIV-1 non-nucleoside reverse transcriptase inhibitors: a patent review (2011–2014)

X Li, L Zhang, Y Tian, Y Song, P Zhan… - Expert opinion on …, 2014 - Taylor & Francis
Introduction: There is a continuous need for next-generation non-nucleoside RT inhibitors
(NNRTIs) with different resistance profiles, improved safety, excellent tolerability, and …

Effect of mutations at position E138 in HIV-1 reverse transcriptase and their interactions with the M184I mutation on defining patterns of resistance to nonnucleoside …

HT Xu, SP Colby-Germinario… - Antimicrobial agents …, 2013 - Am Soc Microbiol
Impacts of mutations at position E138 (A/G/K/Q/R/V) alone or in combination with M184I in
HIV-1 reverse transcriptase (RT) were investigated. We also determined why E138K is the …

[HTML][HTML] Application of 3D-QSAR, pharmacophore, and molecular docking in the molecular design of diarylpyrimidine derivatives as HIV-1 nonnucleoside reverse …

G Liu, W Wang, Y Wan, X Ju, S Gu - International journal of molecular …, 2018 - mdpi.com
Diarylpyrimidines (DAPYs), acting as HIV-1 nonnucleoside reverse transcriptase inhibitors
(NNRTIs), have been considered to be one of the most potent drug families in the fight …

Structural optimization of N1-aryl-benzimidazoles for the discovery of new non-nucleoside reverse transcriptase inhibitors active against wild-type and mutant HIV-1 …

AM Monforte, L De Luca, MR Buemi… - Bioorganic & medicinal …, 2018 - Elsevier
Non-nucleoside reverse transcriptase inhibitors (NNRTIs) are recommended components of
preferred combination antiretroviral therapies used for the treatment of human …

[HTML][HTML] Drug repositioning in Friedreich ataxia

A Rufini, F Malisan, I Condò, R Testi - Frontiers in Neuroscience, 2022 - frontiersin.org
Friedreich ataxia is a rare neurodegenerative disorder caused by insufficient levels of the
essential mitochondrial protein frataxin. It is a severely debilitating disease that significantly …

[HTML][HTML] HIV: how to manage heavily treatment-experienced patients

S Spivack, S Pagkalinawan, R Samuel… - Drugs in …, 2022 - ncbi.nlm.nih.gov
Although decreasing in prevalence, heavily treatment-experienced (HTE) persons with
limited options for HIV treatment present unique complexities, even amongst experienced …

Recent advances in the design and development of non‐nucleoside reverse transcriptase inhibitor scaffolds

P Shirvani, A Fassihi, L Saghaie - ChemMedChem, 2019 - Wiley Online Library
Non‐nucleoside reverse transcriptase inhibitors (NNRTIs) have always been an important
part of the anti‐HIV‐1 combination therapy known as combination antiretroviral therapy …

Agonism of human pregnane X receptor by rilpivirine and etravirine: comparison with first generation non-nucleoside reverse transcriptase inhibitors

D Sharma, AJ Lau, MA Sherman, TKH Chang - Biochemical pharmacology, 2013 - Elsevier
Rilpivirine and etravirine are second generation non-nucleoside reverse transcriptase
inhibitors approved recently by the United States Food and Drug Administration for the …

Insights into the key structural features of N1-ary-benzimidazols as HIV-1 NNRTIs using molecular docking, molecular dynamics, 3D-QSAR, and pharmacophore …

W Wang, Y Tian, Y Wan, S Gu, X Ju, X Luo, G Liu - Structural Chemistry, 2019 - Springer
Abstract N 1-ary-benzimidazol (NABZ) derivatives, an important class of HIV-1
nonnucleoside reverse transcriptase inhibitors (NNRTIs), have been considered as one of …