Molecular Modeling Design Strategy on Novel Drugs for HIV-1 Tat/TAR Complex

2000 ◽  
Vol 28 (5) ◽  
pp. A436-A436
Author(s):  
L. P. Gomes ◽  
L. J. O. Figueiredo ◽  
O. A. C. Antunes
2000 ◽  
Vol 97 (12) ◽  
pp. 6356-6361 ◽  
Author(s):  
L. Zhao ◽  
A. G. Cox ◽  
J. A. Ruzicka ◽  
A. A. Bhat ◽  
W. Zhang ◽  
...  

2012 ◽  
Vol 10 (11) ◽  
pp. 1265-1267 ◽  
Author(s):  
Christopher James Kevin Ward

Tetrahedron ◽  
1997 ◽  
Vol 53 (12) ◽  
pp. 4231-4238 ◽  
Author(s):  
Yvan Boulanger ◽  
Alain Larocque ◽  
Abdesslem Khiat ◽  
François Deschamps ◽  
Gilles Sauvé

2008 ◽  
Vol 16 (6) ◽  
pp. 3039-3048 ◽  
Author(s):  
Cátia Teixeira ◽  
Florent Barbault ◽  
Joseph Rebehmed ◽  
Kun Liu ◽  
Lan Xie ◽  
...  

2014 ◽  
Vol 95 (12) ◽  
pp. 2778-2783 ◽  
Author(s):  
Lauren B. Beach ◽  
Jonathan M. Rawson ◽  
Baek Kim ◽  
Steven E. Patterson ◽  
Louis M. Mansky

Human immunodeficiency virus type 2 (HIV-2) infects about two million people worldwide. HIV-2 has fewer treatment options than HIV-1, yet may evolve drug resistance more quickly. We have analysed several novel drugs for anti-HIV-2 activity. It was observed that 5-azacytidine, clofarabine, gemcitabine and resveratrol have potent anti-HIV-2 activity. The EC50 values for 5-azacytidine, clofarabine and resveratrol were found to be significantly lower with HIV-2 than with HIV-1. A time-of-addition assay was used to analyse the ability of these drugs to interfere with HIV-2 replication. Reverse transcription was the likely target for antiretroviral activity. Taken together, several novel drugs have been discovered to have activity against HIV-2. Based upon their known activities, these drugs may elicit enhanced HIV-2 mutagenesis and therefore be useful for inducing HIV-2 lethal mutagenesis. In addition, the data are consistent with HIV-2 reverse transcriptase being more sensitive than HIV-1 reverse transcriptase to dNTP pool alterations.


2002 ◽  
Vol 20 (3) ◽  
pp. 397-411 ◽  
Author(s):  
Nagarajan Pattabiraman ◽  
Hugo M. Martinez ◽  
Bruce A. Shapiro

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