Bioorganic and Medicinal Chemistry Letters p. 3531 - 3536 (1998)
Update date:2022-08-04
Topics:
Chen, Xiaoqi
Kempf, Dale J.
Sham, Hing L.
Green, Brian E.
Molla, Akhteruzaman
Korneyeva, Marina
Vasavanonda, Sudthida
Wideburg, Norman E.
Saldivar, Ayda
Marsh, Kennan C.
McDonald, Edith
Norbeck, Daniel W.
The 2-isopropyl thiazolyl group is a highly optimized P3 ligand for C2 symmetry-based HIV protease inhibitors, as exemplified in the drag ritonavir. Here we report that incorporation of this P3 ligand into a piperazine hydroxyethylamine series also yielded novel, highly potent inhibitors. In tissue culture assays, the presence of human serum was less deleterious to the activity of these inhibitors than to that of ritonavir. Furthermore, potent activity against ritonavir resistant HIV was observed.
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