The design and synthesis of diaryl ether second generation HIV-1 non-nucleoside reverse transcriptase inhibitors (NNRTIs) with enhanced potency versus key clinical mutations

2008 ◽  
Vol 18 (9) ◽  
pp. 2959-2966 ◽  
Author(s):  
Thomas J. Tucker ◽  
Sandeep Saggar ◽  
John T. Sisko ◽  
Robert M. Tynebor ◽  
Theresa M. Williams ◽  
...  
2014 ◽  
Vol 22 (4) ◽  
pp. 1459-1467 ◽  
Author(s):  
Anna-Maria Monforte ◽  
Stefania Ferro ◽  
Laura De Luca ◽  
Giuseppa Lo Surdo ◽  
Francesca Morreale ◽  
...  

Author(s):  
Sahana Pai ◽  
Jayesh Mudgal ◽  
B. Venkatesh Kamath ◽  
K. Sreedhara Ranganath Pai

AbstractHuman immunodeficiency virus-1 (HIV-1) infection remains to be one of the major threats throughout the world. Many researchers are working in this area to find a cure for HIV-1. The group of the FDA approved drugs which are currently used against HIV-1 in the clinical practice include nucleoside reverse transcriptase inhibitors (NRTIs), non-nucleoside reverse transcriptase inhibitors (NNRTIs), integrase inhibitors (InIs), and protease inhibitors (PIs). Fixed dose combinations (FDCs) of these drugs are available and are used as per the anti-retroviral therapy (ART) guidelines. Despite these, unfortunately, there is no cure for HIV1 infection to date. The present review is focused upon describing the importance of a post-transcriptional regulatory protein “Rev”, responsible for latent HIV-1 infection as a possible, and promising therapeutic target against HIV-1.


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