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Title:
置換されたアリールチオウレアおよび関連化合物;ウイルス複製のインヒビター
Document Type and Number:
Japanese Patent JP4206382
Kind Code:
B2
Abstract:
The invention provides compounds and pharmaceutically acceptable salts of Formula I wherein the variables A1, A2, R1, R2, V, W, X, Y, and Z are defined herein. Certain compounds of Formula I described herein which possess potent antiviral activity. The invention particularly provides compounds of Formula I that are potent and/or selective inhibitors of Hepatitis C virus replication. The invention also provides pharmaceutical compositions containing one or more compound of Formula I, or a salt, solvate, or acylated prodrug of such compounds, and one or more pharmaceutically acceptable carriers, excipients, or diluents. The invention further comprises methods of treating patients suffering from certain infectious diseases by administering to such patients an amount of a compound of Formula I effective to reduce signs or symptoms of the disease or disorder. These infectious diseases include viral infections, particularly HCV infections. The invention is particularly includes methods of treating human patients suffering from an infectious disease, but also encompasses methods of treating other animals, including livestock and domesticated companion animals, suffering from an infectious disease. Methods of treatment include administering a compound of Formula I as a single active agent or administering a compound of Formula I in combination with on or more other therapeutic agent.

Inventors:
Chen, Dawei
Deshpande, Mylind
Andrew, Turkauf
Paduke, Avinash
One, sheangs
Shen, Yupin
Riu, quisian
Queen, Jesse
Oukanda, Junko
Li, Shaumin
Application Number:
JP2004553861A
Publication Date:
January 07, 2009
Filing Date:
November 18, 2003
Export Citation:
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Assignee:
Achillion Pharmaceuticals, Incorporated
International Classes:
C07C335/26; A61K31/17; A61K31/24; A61K31/245; A61K31/343; A61K31/353; A61K31/357; A61K31/36; A61K31/381; A61K31/40; A61K31/4015; A61K31/404; A61K31/41; A61K31/4162; A61K31/4164; A61K31/4192; A61K31/42; A61K31/423; A61K31/4245; A61K31/428; A61K31/433; A61K31/4402; A61K31/4406; A61K31/445; A61K31/47; A61K31/4965; A61K31/519; A61K31/5377; A61K31/55; A61P1/16; A61P31/14; C07D207/16; C07D207/34; C07D209/42; C07D209/48; C07D211/10; C07D211/62; C07D211/70; C07D211/86; C07D213/64; C07D213/65; C07D213/81; C07D215/06; C07D215/38; C07D217/04; C07D233/42; C07D233/90; C07D239/26; C07D241/24; C07D249/04; C07D257/04; C07D261/18; C07D263/34; C07D271/08; C07D271/12; C07D277/56; C07D277/62; C07D277/68; C07D285/06; C07D295/12; C07D295/135; C07D295/14; C07D295/15; C07D307/52; C07D307/68; C07D307/85; C07D311/24; C07D311/58; C07D317/66; C07D319/20; C07D333/20; C07D333/34; C07D333/62; C07D333/70; C07D405/12; C07D407/12; C07D409/12; C07D413/12; C07D417/04; C07D417/12; C07D487/04; C07D495/04
Domestic Patent References:
JP2002537298A
JP2001526255A
JP7285952A
JP9504278A
JP6184162A
JP5507686A
JP2229148A
JP2256661A
JP1168661A
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Foreign References:
WO2001097786A1
WO2000025780A1
US4617316
DE3504016A
US3803227
Other References:
Bioorganic & Medicinal Chemistry Letters,2001年,11(17),p.2225-2228
Indian Journal of Chemistry, Section B,1995年,34B(3),p.201-208
Chinese Journal of Medicinal Chemistry,2002年,12(4),p.200-204
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Chinese Journal of Applied Chemistry,1992年,9(4),p.35-40
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Synthesis,1988年,(6),p.456-459
Journal of the Pharmaceutical Society of Korea,1973年,17(4),p.223-234
Chimica Therapeutica,1966年,(7),p.421-424
Attorney, Agent or Firm:
Takeshi Oshio