US2016250233A1PendingUtilityA1
Antiviral drugs for treatment or prevention of dengue infection
Est. expiryMay 23, 2027(~0.9 yrs left)· nominal 20-yr term from priority
A61P 31/14A61P 31/12C07D 405/12A61K 31/635C07D 253/08C07D 239/96C07C 311/46A61K 31/522C07D 491/048A61K 31/502A61K 31/18C07D 401/12A61K 31/473A61K 9/0019A61K 31/519A61K 31/53C07D 403/06C07D 409/12C07D 417/12C07D 239/88A61K 31/63C07D 237/32C07D 241/44A61K 31/517C07D 473/08C07D 221/14C07D 495/04Y02A50/30
50
PatentIndex Score
0
Cited by
0
References
0
Claims
Abstract
Compounds, methods and pharmaceutical compositions for treating viral infections, by administering certain compounds in therapeutically effective amounts are disclosed. Methods for preparing the compounds and methods of using the compounds and pharmaceutical compositions thereof are also disclosed. In particular, the treatment and prophylaxis of viral infections such as caused by flavivirus is disclosed, i.e., including but not limited to, Dengue virus, West Nile virus, yellow fever virus, Japanese encephalitis virus, and tick-borne encephalitis virus.
Claims
exact text as granted — not AI-modified1 .- 36 . (canceled)
37 . A pharmaceutical composition comprising a pharmaceutically acceptable carrier and a compound having the following general formula I or a pharmaceutically acceptable salt thereof:
wherein R 1 and R 2 are independently hydrogen, alkyl, alkenyl, alkynyl, or unsubstituted or substituted cycloalkyl, arylalkyl, aryl, or R 1 and R 2 together may form a substituted or unsubstituted ring, which may include one or more heteroatoms in the ring; and
Ar is substituted or unsubstituted aryl or heteroaryl;
said cycloalkyl, arylalkyl, and aryl group substituents being one or more radical(s) independently selected from the group consisting of a straight- or branched chain alkyl, alkoxy, alkoxyalkyl, alkoxyalkoxy, halogen, polyfluoroalkyl, polyfluoroalkoxy, carboxy, cyano, nitro, amido, amidoalkyl, carboxamide, alkylthio, alkylsulfinyl, alkylsulfonyl, sulfonamide, and mercapto
wherein the compound of formula I is selected from 2-(6-Chloro-4-oxo-4H-quinazolin-3-yl)-N4-[4-(isopropyl-methyl-sulfamoyl)-phenyl]-acetamide; 2-(7-Fluoro-4-oxo-4H-quinazolin-3-yl)-N-[4-(isopropyl-methyl-sulfamoyl)-phenyl]-acetamide; N-[4-(2,6-Dimethyl-piperidine-1-sulfonyl)-phenyl]-2-(4-oxo-4H-quinazolin-3-yl)-acetamide; N-[4-(3,5-Dimethyl-piperidine-1-sulfonyl)-phenyl]-2-(4-oxo-4H-quinazolin-3-yl)-acetamide; N-[4-(2,6-Dimethyl-piperidine-1-sulfonyl)-phenyl]-2-(4-oxo-4H-thieno[2,3-d]pyrimidin-3-yl)-acetamide; and 2-(4-oxo-4H-quinazolin-3-yl)-N-[4-(2,2,2-trifluoro-ethylsulfamoyl)-phenyl]-acetamide.
38 . The pharmaceutical composition according to claim 37 , wherein said pharmaceutical composition is suitable for administration in a human or animal, wherein said administration is selected from the group consisting of: oral administration, rectal administration, parenteral administration, intravaginal administration, intraperitoneal administration and administration by inhalation.
39 . The pharmaceutical composition according to claim 37 , wherein said pharmaceutically acceptable carrier is solid.
40 . The pharmaceutical composition according to claim 37 , wherein said pharmaceutically acceptable carrier is liquid.
41 . The pharmaceutical composition according to claim 38 , wherein said parenteral administration is selected from the group consisting of: intramuscular injection, subcutaneous injection and intravenous infusion.Cited by (0)
No later patents cite this yet.
References (0)
No backward citations on record.