http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CA-2232267-C

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P43-00
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D521-00
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filingDate 1996-07-24-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2002-06-11-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_eb568b0ef468eb9db887f4904917f5f7
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_aacc79a3f1231e7100f6b89dd2720a9a
publicationDate 2002-06-11-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CA-2232267-C
titleOfInvention Novel imidazole lipoxygenase inhibitors
abstract The present invention provides a compound of formula (I) and a pharmaceutically acceptable salt thereof, wherein Ar is phenylene optionally substituted with halo, hydroxy, cyano, amino, C1-C4 alkyl, C1-C4 alkoxy, C1- C4 alkylthio, C1-C4 halo-substituted alkyl or C1-C4 halo-substituted alkoxy; X is -A-X1- or -X1-A-, wherein A is a direct bond or C1-C4 alkylene, and X1 is ox y, thio, sulfinyl or sulfonyl; Ar1 is phenylene, pyridylene or thienylene optionally substituted with halo, hydroxy, cyano, nitro, amino, C1-C4 alkyl, C1-C4 alkoxy, C1-C4 alkylthio, C1-C4 halo-substituted alkyl, C1-C4 halo- substituted alkoxy, C1-C4 alkylamino or di(C1-C4)alkylamino; Y is CN or CONR1R2 wherein R1 and R2 are independently hydrogen or C1-C4 alkyl; and R i s hydrogen or C1-C6 alkyl; W is C2-C3 alkylene, one carbon atom of which may b e replaced by an oxygen atom. Further the invention provides a pharmaceutical composition for treating an inflammatory disease, allergy or cardiovascular diseases or the like in a mammalian subject which comprises a compound of formula (I) and a pharmaceutically acceptable carrier.
priorityDate 1995-09-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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