Three series (6, 13, and 14) of new diarylaniline (DAAN) analogues were designed, synthesized, and evaluated for anti-HIV potency, especially against the E138K viral strain with a major mutation conferring resistance to the new-generation non-nucleoside reverse transcriptase inhibitor drug rilpivirine (1b). Promising new compounds were then assessed for physicochemical and associated pharmaceutical properties, including aqueous solubility, log P value, and metabolic stability, as well as predicted lipophilic parameters of ligand efficiency, ligand lipophilic efficiency, and ligand efficiency-dependent lipophilicity indices, which are associated with ADME property profiles. Compounds 6a, 14c, and 14d showed high potency against the 1b-resist...
Nineteen new halogenated diarylpyridinamine (DAPA) analogues (6a-n and 8a-e) modified on the phenoxy...
By means of structure-based molecular hybridization strategy, a series of novel diarylpyri(mi)dine d...
Through a structure-based molecular hybridization approach, a novel series of diarylnicotinamide der...
Three series (<b>6</b>, <b>13</b>, and <b>14</b>) of new diarylaniline (DAAN) analogues were designe...
Using physicochemical property-driven optimization, twelve new diarylaniline compounds (DAANs) (7a–h...
The current optimization of 2,4-diarylaniline analogs (DAANs) on the central phenyl ring provided a ...
Twenty-one new 4-substituted diarylaniline compounds (DAANs) (Scheme 2, series 13, 14, and 15) were ...
Based on the structures and activities of our previously identified non-nucleoside reverse transcrip...
By using structure-based drug design and isosteric replacement, diarylaniline and 1,5-diarylbenzene-...
Non-nucleoside inhibitors of HIV-1 reverse transcriptase are reported that have ca. 100-fold greater...
The recently approved anti-AIDS drug rilpivirine (TMC278, Edurant) is a nonnucleoside inhibitor (NNR...
Two series (4 and 5) of diarylpyridine derivatives were designed, synthesized, and evaluated for ant...
Non-nucleoside reverse transcriptase inhibitors (NNRTIs) represent an indispensable part of anti-HIV...
Nineteen new halogenated diarylpyridinamine (DAPA) analogues (6a-n and 8a-e) modified on the phenoxy...
By means of structure-based molecular hybridization strategy, a series of novel diarylpyri(mi)dine d...
Through a structure-based molecular hybridization approach, a novel series of diarylnicotinamide der...
Three series (<b>6</b>, <b>13</b>, and <b>14</b>) of new diarylaniline (DAAN) analogues were designe...
Using physicochemical property-driven optimization, twelve new diarylaniline compounds (DAANs) (7a–h...
The current optimization of 2,4-diarylaniline analogs (DAANs) on the central phenyl ring provided a ...
Twenty-one new 4-substituted diarylaniline compounds (DAANs) (Scheme 2, series 13, 14, and 15) were ...
Based on the structures and activities of our previously identified non-nucleoside reverse transcrip...
By using structure-based drug design and isosteric replacement, diarylaniline and 1,5-diarylbenzene-...
Non-nucleoside inhibitors of HIV-1 reverse transcriptase are reported that have ca. 100-fold greater...
The recently approved anti-AIDS drug rilpivirine (TMC278, Edurant) is a nonnucleoside inhibitor (NNR...
Two series (4 and 5) of diarylpyridine derivatives were designed, synthesized, and evaluated for ant...
Non-nucleoside reverse transcriptase inhibitors (NNRTIs) represent an indispensable part of anti-HIV...
Nineteen new halogenated diarylpyridinamine (DAPA) analogues (6a-n and 8a-e) modified on the phenoxy...
By means of structure-based molecular hybridization strategy, a series of novel diarylpyri(mi)dine d...
Through a structure-based molecular hybridization approach, a novel series of diarylnicotinamide der...