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filingDate 1996-04-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2002-01-01-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b932868f0309fc6f60ea78e83e829771
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e1cd75a8f4cfedd4be0956d8e53b5d03
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_67308d0eb3fb02adeb3a4d1d4fa8ccf7
publicationDate 2002-01-01-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber TW-470750-B
titleOfInvention Reversible cysteine protease inhibitors
abstract A compound which is a cysteine protease inhibitor of formula 1, in which: n is 0 to 2; A-B represents a linkage of -C(O)NH-; X represents a bond, methylene or the linkage -CH2CH(R4)-, wherein R4 is hydrogen or C1-4 alkyl; Y is -NH-; Z is -C(R6)(R7)- wherein R6 is hydrogen or methyl and R7 is as defined below; Z1 is -C(R5)(R8)-, wherein R6 is hydrogen or methyl and R8 is as defined below; R1 is morpholinecarbonyl, phenyl-C1-6 alkyl-carbonyl, or C1-6 alkyl-carbonyl wherein the C1-6 alkyl is optionally substituted with carboxyl group or C1-4 alkyl ester of the carboxyl group; R7 is hydrogen, C1-6 alkyl or phenyl- or napthyl-C1-6-alkyl optionally substituted with hydroxyl on the phenyl or rapthyl moiety, R8 is hydrogen, phenyl-C1-6 alkyl, or carboxy-C1-6 alkyl; and R2 is hydrogen, C1-6 alkyl optionally substituted with one or more radicals selected from halo, phenyl, napthyl, phenyl-C1-6 alkyl, or napthyl-C1-6-alkyl; and the pharmaceutically acceptable salts, individual isomers and mixtures of isomers thereof.
priorityDate 1995-03-24-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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Total number of triples: 433.