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Synthesis of potent and orally active HIV-protease inhibitors
H G Capraro1, G Bold, A Fässler
1Ciba-Geigy Ltd., Basel, Switzerland.
Archiv Der Pharmazie
|June 1, 1996
Abstract:
A series of potent HIV-protease inhibitors has been prepared. Several of the newly synthesized compounds showed high plasma even after oral administration to animals. Based on the overall biological profile, CGP 61755 was chosen for further preclinical evaluation. For this compound, a 10 step synthesis potentially suitable for large scale production was developed.