A synthesis program directed toward improving the stability of imidoyl thiourea based non-nucleoside reverse transcriptase inhibitors (NNRTIs) led to the discovery of diaryltriazines (DATAs), a new class of potent NNRTIs. The synthesis and anti-HIV structure-activity relationship (SAR) studies of a series of DATA derivatives are described.status: publishe
Guided by crystal structures of HIV-1 RT/DAPY complex and molecular modeling studies, a series of no...
On the basis of structural features, binding mode, and structure-activity relationship studies of tw...
On the basis of structural features, binding mode, and structure-activity relationship studies of tw...
The synthesis and anti-HIV-1 activity of a series of diarylpyrimidines (DAPYs) are described. Severa...
Stemming from work on a previous clinical candidate, loviride, and other alpha-APA derivatives, a ne...
In continuation of our efforts toward identification and optimization of novel non-nucleoside revers...
In order to improve the positional adaptability of our previously reported naphthyl diaryltriazines ...
This article reports the design, synthesis and antiviral evaluation of a new series of non-nucleosid...
By means of structure-based molecular hybridization strategy, a series of novel diarylpyri(mi)dine d...
This article reports the design, synthesis and antiviral evaluation of a new series of non-nucleosid...
By means of structure-based molecular hybridization strategy, a series of novel diarylpyri(mi)dine d...
As a continuation of our efforts to discover and develop "me-better" drugs of DAPYs, novel diarylpyr...
Antiviral agents: A series of CN-CH2-DAPY analogues were identified as novel non-nucleoside reverse ...
A series of novel 4,6-diarylpyrimidines (4,6-DAPY) and diarylbenzenes (DABE) compounds were synthesi...
Guided by crystal structures of HIV-1 RT/DAPY complex and molecular modeling studies, a series of no...
Guided by crystal structures of HIV-1 RT/DAPY complex and molecular modeling studies, a series of no...
On the basis of structural features, binding mode, and structure-activity relationship studies of tw...
On the basis of structural features, binding mode, and structure-activity relationship studies of tw...
The synthesis and anti-HIV-1 activity of a series of diarylpyrimidines (DAPYs) are described. Severa...
Stemming from work on a previous clinical candidate, loviride, and other alpha-APA derivatives, a ne...
In continuation of our efforts toward identification and optimization of novel non-nucleoside revers...
In order to improve the positional adaptability of our previously reported naphthyl diaryltriazines ...
This article reports the design, synthesis and antiviral evaluation of a new series of non-nucleosid...
By means of structure-based molecular hybridization strategy, a series of novel diarylpyri(mi)dine d...
This article reports the design, synthesis and antiviral evaluation of a new series of non-nucleosid...
By means of structure-based molecular hybridization strategy, a series of novel diarylpyri(mi)dine d...
As a continuation of our efforts to discover and develop "me-better" drugs of DAPYs, novel diarylpyr...
Antiviral agents: A series of CN-CH2-DAPY analogues were identified as novel non-nucleoside reverse ...
A series of novel 4,6-diarylpyrimidines (4,6-DAPY) and diarylbenzenes (DABE) compounds were synthesi...
Guided by crystal structures of HIV-1 RT/DAPY complex and molecular modeling studies, a series of no...
Guided by crystal structures of HIV-1 RT/DAPY complex and molecular modeling studies, a series of no...
On the basis of structural features, binding mode, and structure-activity relationship studies of tw...
On the basis of structural features, binding mode, and structure-activity relationship studies of tw...