http://rdf.ncbi.nlm.nih.gov/pubchem/patent/KR-20080033475-A

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filingDate 2006-07-28^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_85739b5bc85615598ae1f04879491094
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publicationDate 2008-04-16^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber KR-20080033475-A
titleOfInvention Macrocyclic Inhibitors of Hepatitis C Virus
abstract A compound of formula (I), an N-oxide, salt, or stereoisomer thereof (A represents OR 1 , NHS (═O) p R 2 ; wherein R 1 is hydrogen, C 1 -C 6 alkyl, C 0 -C 3 alkylenecarbocyclyl, C 0 -C 3 alkyleneheterocyclyl; R 2 is C 1 -C 6 alkyl, C 0 -C 3 alkylenecarbocyclyl, C 0 -C 3 alkylene Heterocyclyl; p independently represents 1 or 2; n represents 3, 4, 5 or 6; ----- represents any double bond; L represents N or CRz; Rz Is H or forms a double bond with an asterisk carbon; Rq is H, or when L is CRz, Rq may be C 1 -C 6 alkyl; Rr is C 1 -C 6 alkyl, C 1 -C 6 alkoxy, hydroxy, halo, haloC 1 -C 6 alkyl, amino, mono- or dialkylamino, mono- or dialkylaminocarbonyl, C 1 -C 6 alkylcarbonyl-amino, C 0 -C 3 Alkylene Carbocyclyl and C 0 -C 3 Alkylene Heterocyclo Quinazolinyl optionally substituted with one or two or three substituents each independently selected from kyl; R 5 represents hydrogen, C 1 -C 6 alkyl, C 1 -C 6 alkoxyC 1 -C 6 alkyl or C 3- C 7 cycloalkyl; R 6 represents hydrogen, C 1 -C 6 alkyl, C 1 -C 6 alkoxy, C 0 -C 3 alkylenecarbocyclyl, C 0 -C 3 alkyleneheterocyclyl, hydroxy , Bromo, chloro or fluoro) have utility in the treatment or prevention of flaviviruses, such as HCV infection.
priorityDate 2005-07-29^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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