scholarly journals R88-APOBEC3Gm Inhibits the Replication of Both Drug-resistant Strains of HIV-1 and Viruses Produced From Latently Infected Cells

2014 ◽  
Vol 3 ◽  
pp. e151 ◽  
Author(s):  
Xiaoxia Wang ◽  
Zhujun Ao ◽  
Kallesh Danappa Jayappa ◽  
Bei Shi ◽  
Gary Kobinger ◽  
...  
2003 ◽  
Vol 26 (2) ◽  
pp. 153-161 ◽  
Author(s):  
Palanee Ammaranond ◽  
Philip Cunningham ◽  
Robert Oelrichs ◽  
Kazuo Suzuki ◽  
Claire Harris ◽  
...  

AIDS ◽  
2003 ◽  
Vol 17 ◽  
pp. S31-S38 ◽  
Author(s):  
Laurence Vergne ◽  
Coumba Touré Kane ◽  
Christian Laurent ◽  
Ndella Diakhaté ◽  
Ndeye Fatou Ngom Gueye ◽  
...  

2017 ◽  
Vol 71 ◽  
pp. 211-218 ◽  
Author(s):  
Rahul Suryawanshi ◽  
Sushama Jadhav ◽  
Nandini Makwana ◽  
Dipen Desai ◽  
Devidas Chaturbhuj ◽  
...  

2020 ◽  
Vol 12 (9) ◽  
pp. 775-794 ◽  
Author(s):  
Mei Zhu ◽  
Ling Ma ◽  
Biao Dong ◽  
Guoning Zhang ◽  
Juxian Wang ◽  
...  

Aim: HIV-1 protease inhibitors regimens suffered from a number of drawbacks, among which, the most egregious issue was the growing emergence of drug-resistant strains. Materials & methods: The design strategy of maximizing the protease active site interactions with the inhibitor, especially promoting extensive hydrogen bonding with the protein backbone atoms, might be in favor of combating drug resistance. A series of HIV-1 protease inhibitors that incorporated enantiomeric isopropanols as the P1′ ligands in combination with phenols as the P2 ligands were reported herein. Results: A number of inhibitors displayed potent protease enzyme inhibition activity. In particular, inhibitor 14c showed comparable potency as darunavir with IC50 value of 1.91 nM and activity against darunavir-resistant HIV-1 variants. Conclusion: The new kind of HIV-1 protease inhibitors deserves further study.


PLoS ONE ◽  
2010 ◽  
Vol 5 (6) ◽  
pp. e10976 ◽  
Author(s):  
Victoria L. Demetriou ◽  
David A. M. C. van de Vijver ◽  
Ioanna Kousiappa ◽  
Claudia Balotta ◽  
Bonaventura Clotet ◽  
...  

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