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filingDate 2002-06-07^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c1084fc28e725215adae8805cf0a3c2a
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a706bad6da3b4481f8829f6c7c4bf64c
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_26ffc7a3a60d5771f108856b785f719e
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b0683157a0386d5c78660d5d3d7744eb
publicationDate 2006-06-30^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber NZ-532926-A
titleOfInvention Urea substituted imidazopyridines and pharmaceutical compositions for inducing cytokine biosynthesis and treating viral and neoplastic diseases
abstract A compound of formula (I) is described wherein: X is alkylene or alkenylene; Y is -CO- or -CS-; Z is -NR6-, -NR6-CO-, -NR6-SO2- or -NR7-; R1 is aryl, heteroaryl, heterocyclyl, alkyl or alkenyl each which may be unsubstituted or substituted; R2 is selected from H, alkyl, alkenyl, aryl, substituted aryl, heteroaryl, substituted heteroaryl, alkyl-O-alkyl, alkyl-S-alkyl, alkyl-O-aryl, alkyl-S-aryl, alkyl-O-alkenyl, alkyl-S-alkenyl and alkyl or alkenyl substituted; R3 and R4 are selected from hydrogen, alkyl, alkenyl, halogen, alkoxy, amino, alkylamino, dialkylamino and alkylthio; R5 is H or C1-10 alkyl, or R5 can join with X to form a ring that contains one or two hetero atoms; R6 is H or C1-10alkyl; R7 is H or C1-10alkyl which may be interrupted by a heteroatom or when R1 is alkyl, R7 and R1 can join to form a ring. A pharmaceutical composition comprising the compound is useful for inducing cytokine biosynthesis, in treating viral disease and for treating a neoplastic disease.
priorityDate 2001-12-06^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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