Classical target-based, high-throughput screening has been useful for the identification of inhibitors for known molecular mechanisms involved in the HIV life cycle. In this study, the development of a cell-based assay that uses a phenotypic drug discovery approach based on automated high-content screening is described. Using this screening approach, the antiviral activity of 26,500 small molecules from a relevant chemical scaffold library was evaluated. Among the selected hits, one sulfonamide compound showed strong anti-HIV activity against wild-type and clinically relevant multidrug resistant HIV strains. The biochemical inhibition, point resistance mutations and the activity of structural analogs allowed us to understand the mode of act...
Acquired immunodeficiency syndrome (AIDS) is a life threatening disease of the human immune system c...
Background. The human immunodeficiency virus type 1 (HIV-1) Reverse transcriptase (RT) with its two ...
Twenty-seven derivatives (40-66) were generated by pharmacophore fusing of sulfonylacetanilide-diary...
Classical target-based, high-throughput screening has been useful for the identification of inhibito...
<div><p>Classical target-based, high-throughput screening has been useful for the identification of ...
We report the first application of ligand-based virtual screening (VS) methods for discovering new c...
We report the first application of ligand-based virtual screening (VS) methods for discovering new c...
Non-nucleoside reverse transcriptase inhibitors (NNRTIs) are potent anti-HIV chemotherapeutics. Alth...
A novel scaffold inhibiting wild type and drug resistant variants of human immunodeficiency virus ty...
International audienceTwo decades after its discovery the human immunodeficiency virus (HIV) is stil...
A novel sulfanyltriazole was discovered as an HIV-1 non-nucleoside reverse transcriptase inhibitor v...
Fragment-based screening methods can be used to discover novel active site or allosteric inhibitors ...
Indolyl aryl sulfone (IAS) non-nucleoside reverse transcriptase (RT) inhibitors (NNRTIs) have been p...
The emergence of drug-resistant strains of human immunodeficiency virus (HIV) threatens the efficacy...
Background. The human immunodeficiency virus type 1 (HIV-1) Reverse transcriptase (RT) with its two ...
Acquired immunodeficiency syndrome (AIDS) is a life threatening disease of the human immune system c...
Background. The human immunodeficiency virus type 1 (HIV-1) Reverse transcriptase (RT) with its two ...
Twenty-seven derivatives (40-66) were generated by pharmacophore fusing of sulfonylacetanilide-diary...
Classical target-based, high-throughput screening has been useful for the identification of inhibito...
<div><p>Classical target-based, high-throughput screening has been useful for the identification of ...
We report the first application of ligand-based virtual screening (VS) methods for discovering new c...
We report the first application of ligand-based virtual screening (VS) methods for discovering new c...
Non-nucleoside reverse transcriptase inhibitors (NNRTIs) are potent anti-HIV chemotherapeutics. Alth...
A novel scaffold inhibiting wild type and drug resistant variants of human immunodeficiency virus ty...
International audienceTwo decades after its discovery the human immunodeficiency virus (HIV) is stil...
A novel sulfanyltriazole was discovered as an HIV-1 non-nucleoside reverse transcriptase inhibitor v...
Fragment-based screening methods can be used to discover novel active site or allosteric inhibitors ...
Indolyl aryl sulfone (IAS) non-nucleoside reverse transcriptase (RT) inhibitors (NNRTIs) have been p...
The emergence of drug-resistant strains of human immunodeficiency virus (HIV) threatens the efficacy...
Background. The human immunodeficiency virus type 1 (HIV-1) Reverse transcriptase (RT) with its two ...
Acquired immunodeficiency syndrome (AIDS) is a life threatening disease of the human immune system c...
Background. The human immunodeficiency virus type 1 (HIV-1) Reverse transcriptase (RT) with its two ...
Twenty-seven derivatives (40-66) were generated by pharmacophore fusing of sulfonylacetanilide-diary...