
Chemical and Pharmaceutical Bulletin p. 2636 - 2640 (1994)
Update date:2022-08-04
Topics:
Kitazaki
Asano
Kato
Kishimoto
Itoh
Tripeptide analogues 2 and 3 containing a dioxoethylene moiety were designed based on the characteristic structure of the naturally occurring human immunodeficiency virus (HIV)-I protease inhibitors RPI-856 A, B, C and D (1). The compounds (2, 3) prepared showed high inhibitory activity, comparable to that of RPI-856 A, against HIV-1 protease in vitro.
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Doi:10.1016/S0040-4020(01)88757-3
(1992)Doi:10.1021/ja00037a068
(1992)Doi:10.1002/jms.3093
(2012)Doi:10.1021/ol060735u
(2006)Doi:10.1021/ol302942m
(2012)Doi:10.3762/bjoc.8.171
(2012)