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Syntheses of new modified Phe-Pro peptides. Use of proline replacements in potential HIV inhibitors
M Bouygues1, M Medou, G Quéléver
1Laboratoire de Chimie Biomoléculaire, Faculté des Sciences de Luminy, Université de la Méditerranée, Marseille, France.
Bioorganic & Medicinal Chemistry Letters
|January 1, 1999
Abstract:
The syntheses consisting of replacement of proline amino acid by a 3-pyrrolidinone ring in Phe-Pro analogues are described. Preliminary anti-HIV studies demonstrated the potential activity of this new class of compounds.