A series of 13 hydroxylated 2-arylnaphthalenes have been synthesized and evaluated as HIV-1 integrase inhibitors. 7-(3,4,5-Trihydroxyphenyl)naphthalene-1,2,3-triol 1c revealed chemical instability upon storage, leading to the isolation of a dimer 5c which was also tested. In the 2-arylnaphthalene series, all compounds were active against HIV-1 IN with IC(50)'s within the 1-10muM range, except for 1c and 5c which displayed submicromolar activity. Antiviral activity against HIV-1 replication was measured on 1b-c and 5c. Amongst the tested molecules, only 5c was found to present antiviral properties with a low cytotoxicity on two different cell lines.status: publishe
The discovery and development of novel inhibitors with activity against variants of human immunodefi...
International audienceThe increasing efficiency of HAART has helped to transform HIV/AIDS into a chr...
The present work is an extension of our ongoing efforts towards the development and identification o...
A series of 13 hydroxylated 2-arylnaphthalenes have been synthesized and evaluated as HIV-1 integras...
We report herein further insight into the biological activities displayed by a series of 2-hydroxyis...
Background: Despite the progress in the discovery of antiretroviral compounds for treating HIV-1 inf...
Highly active anti-retroviral therapy (HAART) using reverse transcriptase (RT) and protease (PR) inh...
Combination therapy using reverse transcriptase (RT) and protease (PR) inhibitors is currently the b...
A series of N-aryl-naphthylamines, exemplified by the structures 11-16, were chosen for an in-house ...
International audienceWe report herein further insight into the biological activities displayed by a...
The search for new molecular constructs that resemble the critical two-metal binding pharmacophore a...
Combination therapy using reverse transcriptase (RT) and protease (PR) inhibitors is currently the b...
The development of novel HIV-1 NNRTIs offers the possibility of generating novel structures with inc...
A series of 6-aryl-2,4-dioxo-5-hexenoic acids, were synthesized and tested against HIV-1 in cell-bas...
The synthesis and the assessment of the anti-HIV activity of a set of molecules inspired by the mult...
The discovery and development of novel inhibitors with activity against variants of human immunodefi...
International audienceThe increasing efficiency of HAART has helped to transform HIV/AIDS into a chr...
The present work is an extension of our ongoing efforts towards the development and identification o...
A series of 13 hydroxylated 2-arylnaphthalenes have been synthesized and evaluated as HIV-1 integras...
We report herein further insight into the biological activities displayed by a series of 2-hydroxyis...
Background: Despite the progress in the discovery of antiretroviral compounds for treating HIV-1 inf...
Highly active anti-retroviral therapy (HAART) using reverse transcriptase (RT) and protease (PR) inh...
Combination therapy using reverse transcriptase (RT) and protease (PR) inhibitors is currently the b...
A series of N-aryl-naphthylamines, exemplified by the structures 11-16, were chosen for an in-house ...
International audienceWe report herein further insight into the biological activities displayed by a...
The search for new molecular constructs that resemble the critical two-metal binding pharmacophore a...
Combination therapy using reverse transcriptase (RT) and protease (PR) inhibitors is currently the b...
The development of novel HIV-1 NNRTIs offers the possibility of generating novel structures with inc...
A series of 6-aryl-2,4-dioxo-5-hexenoic acids, were synthesized and tested against HIV-1 in cell-bas...
The synthesis and the assessment of the anti-HIV activity of a set of molecules inspired by the mult...
The discovery and development of novel inhibitors with activity against variants of human immunodefi...
International audienceThe increasing efficiency of HAART has helped to transform HIV/AIDS into a chr...
The present work is an extension of our ongoing efforts towards the development and identification o...