Retroviral protease inhibiting compounds

C - Chemistry – Metallurgy – 07 – D

Patent

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C07D 213/56 (2006.01) A61K 31/00 (2006.01) A61K 38/05 (2006.01) C07C 33/00 (2006.01) C07C 33/46 (2006.01) C07C 43/164 (2006.01) C07C 43/174 (2006.01) C07C 43/205 (2006.01) C07C 43/215 (2006.01) C07C 43/23 (2006.01) C07C 43/30 (2006.01) C07C 43/315 (2006.01) C07C 45/00 (2006.01) C07C 45/29 (2006.01) C07C 45/56 (2006.01) C07C 45/59 (2006.01) C07C 45/62 (2006.01) C07C 45/67 (2006.01) C07C 45/74 (2006.01) C07C 49/215 (2006.01) C07C 53/134 (2006.01) C07C 69/34 (2006.01) C07C 69/65 (2006.01) C07C 69/732 (2006.01)

Patent

CA 2017252

A retroviral protease inhibiting compound of the formula A-X-B or a pharmaceutically acceptable salt, prodrug or ester thereof, wherein X is a linking group; A is (1) substituted amino, (2) substituted carbonyl, (3) functionalized imino, (4) functionalized alkyl, (5) functionalized acyl, (6) functionalized heterocyclic or (7) functionalized (heterocyclic)alkyl; and B is (1) substituted carbonyl independently defined as herein, (2) substituted amino independently defined as herein, -332- (3) functionalized imino independently defined as herein, (4) functionalized alkyl independently defined as herein, (5) functionalized acyl independently defined as herein, (6) functionalized heterocyclic independently defined as herein or (7) functionalized (heterocyclic)alkyl independently defined as herein.

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