| Literature DB >> 1799953 |
T Mimoto1, J Imai, S Tanaka, N Hattori, S Kisanuki, K Akaji, Y Kiso.
Abstract
HIV-1 protease inhibitors containing allophenylnorstatine [Apns; (2S,3S)-3-amino-2-hydroxy-4-phenylbutyric acid]-Pro (syn diastereomer) as a transition-state mimic were established to be potent and highly selective. Z-Asn-Apns-Pro-NHBut (KNI-102) is the only tripeptide exhibiting substantial anti-HIV activity and may be of minimum size for potent, selective inhibition of HIV protease. Ready availability due to its simple chemical structure and stability should make it valuable for studies of the development of metabolically stable anti-AIDS drugs.Entities:
Mesh:
Substances:
Year: 1991 PMID: 1799953 DOI: 10.1248/cpb.39.3088
Source DB: PubMed Journal: Chem Pharm Bull (Tokyo) ISSN: 0009-2363 Impact factor: 1.645