EP 0538374 A4 19930519 - ASPARTIC PROTEASE INHIBITORS
Title (en)
ASPARTIC PROTEASE INHIBITORS
Publication
Application
Priority
US 54946090 A 19900706
Abstract (en)
[origin: WO9200954A1] Compounds useful as inhibitors of retroviral proteases characterized by structure (I) wherein X<1> and X<2> may consist of 0-2 alpha -amino acid groups terminally substituted by hydrogen or one of a number of end groups, R<1>, R<2> can be selected from a wide variety of hydrocarbon radicals.
IPC 1-7
IPC 8 full level
A61K 38/55 (2006.01); A61P 31/12 (2006.01); C07F 9/30 (2006.01); C07F 9/32 (2006.01); C07F 9/38 (2006.01); C07F 9/40 (2006.01); C07K 1/113 (2006.01); C07K 5/06 (2006.01); C07K 14/81 (2006.01); A61K 38/00 (2006.01)
CPC (source: EP)
A61P 31/12 (2017.12); C07F 9/301 (2013.01); C07F 9/3211 (2013.01); C07K 5/06191 (2013.01); A61K 38/00 (2013.01)
Citation (search report)
- [E] EP 0435059 A1 19910703 - HOECHST AG [DE]
- [A] JOURNAL OF THE AMERICAN CHEMICAL SOCIETY vol. 106, no. 15, 25 July 1984, WASHINGTON, DC US pages 4282 - 4283 PAUL A. BARTLETT 'Phosphinic Acid Dipeptide Analogues: Potent, Slow-Binding Inhibitors of Aspartic Pepsidases'
- See references of WO 9200954A1
Designated contracting state (EPC)
AT BE CH DE DK ES FR GB GR IT LI LU NL SE
DOCDB simple family (publication)
WO 9200954 A1 19920123; AU 8191091 A 19920204; EP 0538374 A1 19930428; EP 0538374 A4 19930519; JP H05508846 A 19931209
DOCDB simple family (application)
US 9104759 W 19910703; AU 8191091 A 19910703; EP 91913442 A 19910703; JP 51231291 A 19910703