<p>Red, pink, brown, orange circles stand for the first-generation inhibitors, i.e. Saquinavir, Ritonavir, Indinavir, Nelfinavir respectively; Darkgreen, cadetblue, cyan, blue triangles stand for the second-generation ones, i.e. Darunavir, Tipranavir, TMC-126, XV638 respectively. The lines indicate the average values for each of them.</p
<p>A collection of 4,000 compounds synthesized on the basis of known kinase binding sites were scree...
The overall theme of this thesis is a step by step approach for the design and characterization of c...
The human immunodeficiency virus type 1 (HIV-1) has continued to be a global concern. With the new H...
Colored lines depict the concentration-prophylaxis profile for an average drug class-specific slope ...
<p>Scatter plot of primary screening data where the percentage of infected cells was normalized with...
<p>The canonical nomenclature for drug moiety positioning is indicated using telaprevir. Telaprevir ...
<p>Single-point inhibition data for rhodesain (Y-axis, % inhibition at 0.1 µM test compound) as comp...
<p>Each dot represents the percentage inhibition of compounds at concentrations of 50 µM (A), 25 µM ...
<p>Inhibition of tested proteases by compounds Camostat, “Novartis166” and “Novartis848”.</p
Indinavir (Crivaxan®) is a potent inhibitor of the HIV (human immunodeficiency virus) protease. This...
HIV-1 protease plays an important role in the processing of virus infection. Protease is an effectiv...
We studied the pharmacological potential effects of viral components, performed target prediction an...
Retroviral protease inhibitors (PIs) are fundamental pillars in the treatment of HIV infection and a...
Data for one inhibitor at a time were excluded from the dataset and predicted from proteochemometric...
<p>(<b>A</b>) Heat map showing relative percent infection inhibition (left panel) and percent cell n...
<p>A collection of 4,000 compounds synthesized on the basis of known kinase binding sites were scree...
The overall theme of this thesis is a step by step approach for the design and characterization of c...
The human immunodeficiency virus type 1 (HIV-1) has continued to be a global concern. With the new H...
Colored lines depict the concentration-prophylaxis profile for an average drug class-specific slope ...
<p>Scatter plot of primary screening data where the percentage of infected cells was normalized with...
<p>The canonical nomenclature for drug moiety positioning is indicated using telaprevir. Telaprevir ...
<p>Single-point inhibition data for rhodesain (Y-axis, % inhibition at 0.1 µM test compound) as comp...
<p>Each dot represents the percentage inhibition of compounds at concentrations of 50 µM (A), 25 µM ...
<p>Inhibition of tested proteases by compounds Camostat, “Novartis166” and “Novartis848”.</p
Indinavir (Crivaxan®) is a potent inhibitor of the HIV (human immunodeficiency virus) protease. This...
HIV-1 protease plays an important role in the processing of virus infection. Protease is an effectiv...
We studied the pharmacological potential effects of viral components, performed target prediction an...
Retroviral protease inhibitors (PIs) are fundamental pillars in the treatment of HIV infection and a...
Data for one inhibitor at a time were excluded from the dataset and predicted from proteochemometric...
<p>(<b>A</b>) Heat map showing relative percent infection inhibition (left panel) and percent cell n...
<p>A collection of 4,000 compounds synthesized on the basis of known kinase binding sites were scree...
The overall theme of this thesis is a step by step approach for the design and characterization of c...
The human immunodeficiency virus type 1 (HIV-1) has continued to be a global concern. With the new H...