AbstractHIV-1 integrase (IN) is a potential target for developing drugs against AIDS. In this letter, QM/MM approach was used to study the inhibition of IN by 5CITEP inhibitor in presence of divalent cations (Mg2+ or Mn2+). In addition, the main interactions occurring in 5CITEP-IN complex and the influence of divalent cations (Mg2+ or Mn2+) in enzymatic inhibition were investigated using B3LYP/6-31+G(d,p)/MM. The results suggest that the Asp64, Asp116 and four crystal water molecules plays a crucial role in cation (Mg2+ or Mn2+) coordination sphere
Metal-activated enzymes are important targets in drug discovery in general and for antivirals in par...
The development of HIV-1 integrase (INT) inhibitors has been hampered by incomplete structural and m...
2-Hydroxyisoquinoline-1,3(2H,4H)-dione was recently discovered as a scaffold for the inhibition of H...
AbstractHIV-1 integrase (IN) is a potential target for developing drugs against AIDS. In this letter...
Most active and selective strand transfer HIV-1 integrase (IN) inhibitors contain chelating function...
Most active and selective strand transfer HIV-1 integrase (IN) inhibitors contain chelating function...
HIV-1 integrase (IN) has been validated as an attractive target for the treatment of HIV/AIDS. Sever...
The integrase enzyme encoded by the human immunodeficiency virus plays an integral role in the viral...
Previously, we synthesized a series of -diketo acid metal complexes as novel HIV-1 integrase (IN) in...
b-Diketo acid-containing compounds are a promising class of human immunodeficiency virus type 1 (HIV...
The mechanism of integrase is generally accepted to be dependant on the presence of two divalent met...
A new target in AIDS therapy development is HIV-1 integrase (IN). It was proven that HIV-1 IN requir...
Data regarding the activity of metal complexes against HIV virus in cell are surprisingly scarce. In...
Human immunodeficiency virus type 1 (HIV-1) infection, still represent a serious global health emerg...
HIV-1 Integrase (IN) represents a very attractive pharmacological target for the development of new ...
Metal-activated enzymes are important targets in drug discovery in general and for antivirals in par...
The development of HIV-1 integrase (INT) inhibitors has been hampered by incomplete structural and m...
2-Hydroxyisoquinoline-1,3(2H,4H)-dione was recently discovered as a scaffold for the inhibition of H...
AbstractHIV-1 integrase (IN) is a potential target for developing drugs against AIDS. In this letter...
Most active and selective strand transfer HIV-1 integrase (IN) inhibitors contain chelating function...
Most active and selective strand transfer HIV-1 integrase (IN) inhibitors contain chelating function...
HIV-1 integrase (IN) has been validated as an attractive target for the treatment of HIV/AIDS. Sever...
The integrase enzyme encoded by the human immunodeficiency virus plays an integral role in the viral...
Previously, we synthesized a series of -diketo acid metal complexes as novel HIV-1 integrase (IN) in...
b-Diketo acid-containing compounds are a promising class of human immunodeficiency virus type 1 (HIV...
The mechanism of integrase is generally accepted to be dependant on the presence of two divalent met...
A new target in AIDS therapy development is HIV-1 integrase (IN). It was proven that HIV-1 IN requir...
Data regarding the activity of metal complexes against HIV virus in cell are surprisingly scarce. In...
Human immunodeficiency virus type 1 (HIV-1) infection, still represent a serious global health emerg...
HIV-1 Integrase (IN) represents a very attractive pharmacological target for the development of new ...
Metal-activated enzymes are important targets in drug discovery in general and for antivirals in par...
The development of HIV-1 integrase (INT) inhibitors has been hampered by incomplete structural and m...
2-Hydroxyisoquinoline-1,3(2H,4H)-dione was recently discovered as a scaffold for the inhibition of H...