Aza-and polyaza-naphthalenly ketones useful as hiv integrase inhibitors
申请人:Zhuang Linghang
公开号:US20050010048A1
公开(公告)日:2005-01-13
Certain aza- and polyaza-naphthalenyl ketones including certain quinolinyl and naphthyridinyl ketones are described as inhibitors of HIV integrase and inhibitors of HIV replication. These compounds are useful in the prevention or treatment of infection by HIV and the treatment or the delay in the onset of AIDS, as compounds or pharmaceutically acceptable salts, or as ingredients in pharmaceutical compositions, optionally in combination with other antivirals, immunomodulators, antibiotics or vaccines. Methods of treating or delaying the onset of AIDS and methods of preventing or treating infection by HIV are also described.
The present invention relates to macrocyclic compounds of formula (I): wherein W, n, m, R
1
, R
2
, R
3
, R
4
, R
5
, R
a
, M, Z and ring B are defined herein, and pharmaceutically acceptable salts thereof, pharmaceutical compositions comprising them, and their use for the treatment or prevention of infection by hepatitis C virus.
申请人:Instituto di Ricerche di Biologia Molecolare P. Angeletti S.p.A.
公开号:US08314062B2
公开(公告)日:2012-11-20
The present invention relates to macrocyclic compounds of formula (I): wherein W, n, m, R1, R2, R3, R4, R5, Ra, M, Z and ring B are defined herein, and pharmaceutically acceptable salts thereof, pharmaceutical compositions comprising them, and their use for the treatment or prevention of infection by hepatitis C virus.