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filingDate 2010-05-11-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2017-12-08-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 2017-12-08-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber KR-101806837-B1
titleOfInvention Uracyl spirooxetane nucleosides
abstract Compounds of formula (I) and all possible stereoisomers thereof; Or a pharmaceutically acceptable salt or solvate thereof; Pharmaceutical preparations; Use of compound (I) as an HCV inhibitor is disclosed: In this formula, R 4 is monophosphate, diphosphate or triphosphate ester; expression Lt; / RTI &gt; R 7 is optionally substituted phenyl; Optionally substituted naphthyl; Or an optionally substituted indolyl; R 8 and R 8 ' are hydrogen, C 1 -C 6 alkyl, benzyl, or phenyl; R 8 and R 8 'taken together with the carbon atom to which they are attached form C 3 -C 7 cycloalkyl; R 9 is C 1 -C 10 alkyl, C 3 -C 7 cycloalkyl, phenyl or phenyl-C 1 -C 6 alkyl, wherein the phenyl moiety of the phenyl or phenyl-C 1 -C 6 alkyl is optionally substituted.
priorityDate 2009-05-14-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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