A number of 1-(2-aminopropyl)-2-mercaptobenzimidazoles related to the TIBO derivatives R82150 have been prepared and tested for their activity against human immunodeficiency virus type 1 (HIV-1). These compounds were all modest inhibitors of the cytophatic effects of HIV-1 in vitro, but only very weak inhibitors of HIV-1 reverse transcriptase (RT).A number of 1-(2-aminopropyl)-2-mercaptobenzimidazole derivatives related to the TIBO derivative R82150 have been prepared and tested for their activity against human immunodeficiency virus type 1 (HIV-1). These compounds are all modest inhibitors of the cytopathic effects of HIV-1 in vitro, but were only weak inhibitors of HIV-1 reverse transcriptase (RT).Peer Reviewedhttp://deepblue.lib.umich.ed...
3,4-Dihydro-2-alkoxy-6-benzyl-4-oxopyrimidines (DABOs) have emerged as non-nucleoside inhibitors of ...
A series of novel benzimidazolones and their analogues, characterized by the presence of one or more...
A series of novel N1-aryl-2-arylthioacetamido-benzimidazoles were synthesized and evaluated as inhib...
Screening of pharmacologically acceptable prototype compounds has recently led to the discovery of a...
In the first paper of this series a new structure with anti-HIV-1 activity was disclosed and analogu...
In previous papers, we have described the discovery of a new series of compounds, 4,5,6,7-tetrahydro...
A series of 1-(2-methyl-4-nitro-imidazol-1-yl)-3-arylamino-propan-2-ones (2a-e), 2-methyl-5-nitro-1-...
TIBO- and TBO-like sulfone derivatives 1 and 2 were designed, synthesized, and tested for their abil...
TIBO- and TBO-like sulfone derivatives 1 and 2 were designed, synthesized, and tested for their abil...
TIBO- and TBO-like sulfone derivatives 1 and 2 were designed, synthesized, and tested for their abil...
A set of new pyrimido[5,4-b]indole derivatives that are structurally related to some non-nucleside H...
TIBO- and TBO-like sulfone derivatives 1 and 2 were designed, synthesized, and tested for their abil...
TIBO- and TBO-like sulfone derivatives 1 and 2 were designed, synthesized, and tested for their abil...
In an ongoing effort to develop novel and potent nonnucleoside HIV-1 reverse transcriptase (RT) inhi...
New 1H,3H-oxazolo[3,4-a]benzimidazoles (OBZs) were synthesized as HIV-1 non-nucleoside reverse trans...
3,4-Dihydro-2-alkoxy-6-benzyl-4-oxopyrimidines (DABOs) have emerged as non-nucleoside inhibitors of ...
A series of novel benzimidazolones and their analogues, characterized by the presence of one or more...
A series of novel N1-aryl-2-arylthioacetamido-benzimidazoles were synthesized and evaluated as inhib...
Screening of pharmacologically acceptable prototype compounds has recently led to the discovery of a...
In the first paper of this series a new structure with anti-HIV-1 activity was disclosed and analogu...
In previous papers, we have described the discovery of a new series of compounds, 4,5,6,7-tetrahydro...
A series of 1-(2-methyl-4-nitro-imidazol-1-yl)-3-arylamino-propan-2-ones (2a-e), 2-methyl-5-nitro-1-...
TIBO- and TBO-like sulfone derivatives 1 and 2 were designed, synthesized, and tested for their abil...
TIBO- and TBO-like sulfone derivatives 1 and 2 were designed, synthesized, and tested for their abil...
TIBO- and TBO-like sulfone derivatives 1 and 2 were designed, synthesized, and tested for their abil...
A set of new pyrimido[5,4-b]indole derivatives that are structurally related to some non-nucleside H...
TIBO- and TBO-like sulfone derivatives 1 and 2 were designed, synthesized, and tested for their abil...
TIBO- and TBO-like sulfone derivatives 1 and 2 were designed, synthesized, and tested for their abil...
In an ongoing effort to develop novel and potent nonnucleoside HIV-1 reverse transcriptase (RT) inhi...
New 1H,3H-oxazolo[3,4-a]benzimidazoles (OBZs) were synthesized as HIV-1 non-nucleoside reverse trans...
3,4-Dihydro-2-alkoxy-6-benzyl-4-oxopyrimidines (DABOs) have emerged as non-nucleoside inhibitors of ...
A series of novel benzimidazolones and their analogues, characterized by the presence of one or more...
A series of novel N1-aryl-2-arylthioacetamido-benzimidazoles were synthesized and evaluated as inhib...