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grantDate 2007-01-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_27b825342650e98ed5c82605ce96caaf
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c9a865748bce229803528af79f59ca6a
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publicationDate 2007-01-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-7169924-B2
titleOfInvention Pyrimidinone derivatives and their use in the treatment of atherosclerosis
abstract Compound of formula (I): n nare disclosed in which:n R 1 is an aryl group, optionally substituted by 1, 2, 3 or 4 substituents which may be the same or different selected from C (1-6) alkyl, C (1-6) alkoxy, C (1-6) alkylthio, hydroxy, halogen, CN, and mono to perfluoro-C (1-4) alkyl; R 2 is halogen, C (1-3) alkyl, C (1-3) alkoxy, hydroxyC (1-3) alkyl, C (1-3) alkylthio, C (1-3) alkylsulphinyl, aminoC (1-3) alkyl, mono- or di-C (1-3) alkylaminoC (1-3) alkyl, C (1-3) alkylcarbonylaminoC (1-3) alkyl, C (1-3) alkoxyC (1-3) alkylcarbonylaminoC (1-3) alkyl, C (1-3) alkylsulphonylaminoC (1-3) alkyl, C (1-3) alkylcarboxy, C (1-3) alkylcarboxyC (1-3) alkyl, and R 3 is hydrogen, halogen, C (1-3) alkyl, or hydroxyC (1-3) alkcyl; or R 2 and R 3 together with the pyrimidone ring carbon atoms to which they are attached form a fused 5-or 6-membered carbocyclic ring; or R 2 and R 3 together with the pyrimidone ring carbon atoms to which they are attached form a fused benzo or heteroaryl ring ring optionally substituted by 1, 2, 3 or 4 substituents which may be the same or different selected from halogen, C (1-4) alkyl, cyano, C (1-6) alkoxy, C (1-6) alkylthio or mono to perfluoro-C (1-4) alkyl; R 4 is hydrogen, C (1-6) alkyl which may be unsubstituted or substituted by 1, 2 or 3 substituents selected from hydroxy, halogen, OR 7 , COR 7 , carboxy, COOR 7 , CONR 9 R 10 , NR 9 R 10 , NR 7 COR 8 , mono- or di-(hydroxyC (1-6) alkyl) amino and N-hydroxyC (1-6) alkyl-N—C (1-6) allkylamino; or R 4 is Het-C (0-4) alkyl in which Het is a 5- to 7- membered heterocyclyl ring comprising N and optionally O or S, and in which N may be substituted by COR 7 , COOR 7 , CONR 9 R 10 , or C (1-6) alkyl optionally substituted by 1, 2 or 3 substituents selected from hydroxy, halogen, OR 7 , COR 7 , carboxy, COOR 7 , CONR 9 R 10 or NR 9 R 10 , for instance, piperidinyl-4-yl, pyrrolidin-3-yl; R 5 is an aryl or a heteroaryl ring optionally substituted by 1, 2, 3 or 4 substituents which may be the same or different selectd from C (1-6) alkyl, C (1-6) alkoxy, C (1-6) alkylthio, arylC (1-6) alkoxy, hydroxy, halogen, CN, COR 7 , carboxy, COOR 7 , NR 7 COR 8 , CONR 9 R 10 , SO 2 NR 9 R 10 , NR 7 SO 2 R 8 , NR 9 R 10 , mono to perfluoro-C (1-4) alkyl and mono to perfluoro-C (1-4) alkoxy; R 6 is an aryl or a heteroaryl ring which is further optionally substituted by 1, 2, 3 or 4 substituents which may be the same or different selected from C (1-18) alkyl, C (1-18) alkoxy, C (1-6) alkylthio, C (1-6) alkylsulfonyl, arylC (1-6) alkoxy, hydroxy, halogen, CN, COR 7 , carboxy, COOR 7 , CONR 9 R 10 , NR 7 COR 8 , SO 2 NR 9 R 10 , NR 7 SO 2 R 8 , NR 9 R 10 , mono to perfluoro-C (1-4) alkyl and mono to perfluoro-C (1-4) alkoxy, or C (5-10) alkyl; These compound are useful for treating diseases associated with abnormal activity of the phospholipase A 2 enzyme, for example athereosclosis.
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http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID77608721
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID229548645
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID249116430
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID23614401
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID239580622
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID247213153
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID229472118
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID44535643
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID23614400
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID239580621
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID420930579
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID44535427
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID229471950
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID239580627
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID247184918
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID249126122
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID69158943
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID128212580
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID239580626
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID2796029
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID412923399
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID23614397
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID420944401
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID49797849
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID412923395
http://rdf.ncbi.nlm.nih.gov/pubchem/gene/GID557037
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID44535424
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID91359942
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID23614396
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID247189162
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID449326692
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID412931179
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID127529797
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID239580610
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID87717122
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID409424171
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID128953223
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID412923415
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID239580604
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID412894236
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID239618225
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID412894181
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID229470200

Total number of triples: 2828.