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filingDate 1992-07-21-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e432015b060e849699081868a1e8ef6d
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_9b885a86aa5d3b86d012c5174210e29f
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a9acf1cfd32faec816f7f20608aa2089
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publicationDate 1994-05-11-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-0596015-A1
titleOfInvention SUBSTITUTED BETA-LACTAM COMPOUNDS FOR USE AS HYPOCHOLESTEROLEMIC AGENTS, AND METHODS OF PREPARATION.
abstract New compounds of formula (I), where A represents -CH = CH-B; -C = C-B; - (CH2) p-X-B, where p is between 0 and 2 and X represents a bond, -NH-, or -S (O) 0-2-; optionally substituted heteroaryl or benzoic fusion heteroaryl; -COB; or (Ia), where k is between 1 and 2; D represents B '- (CH2) mC (O) -, where m is between 1 and 5; B '- (CH2) q-, where q is between 2 and 6; B '- (CH2) eZ- (CH2) r-, where Z represents -O-, -C (O) -, phenylene, -NR8- or -S (O) 0-2-, e is between 0 and 5 and r is between 1 and 5, provided that the sum of e and r is between 1 and 6; B '- (alkenylene) -; B '- (alkadienylene) -; B '- (CH2) t-Z- (alkenylene), where t is between 0 and 3, provided that the sum of t and the number of carbon atoms in the alkenylene chain is between 2 and 6; B '(CH2) f-V- (CH2) g-, where V represents cycloalkylene, f is between 1 and 5 and g is between 0 and 5, provided that the sum of f and g is between 1 and 6; B '- (CH2) tV- (alkenylene) or B- (alkenylene) -V- (CH2) t-, provided that the sum of t and the number of carbon atoms in the alkenylene chain is between 2 and 6 ; B '- (CH2) a-Z- (CH2) b-V- (CH2) d-, where a, b and d are between 0 and 6, provided that the sum of a, b and d is between 0 and 6; T- (CH2) s-, where T represents cycloalkyl and s is between 1 and 6; optionally substituted naphthylmethyl or heteroarylmethyl; B represents optionally substituted phenyl; B 'represents naphthyl, optionally substituted heteroaryl or optionally substituted phenyl; R represents hydrogen, fluoro, alkyl, alkenyl, alkynyl or B- (CH2) h-, where h is between 0 and 3; R4 represents indanyl, benzofuranyl, tetrahydronaphthyl, pyridyl, pyrazinyl, pyrimidinyl, quinolyl or optionally substituted phenyl. The use of these compounds as hypocholesterolemia agents is also described, as well as compounds of formula (II), where R20 represents optionally substituted phenyl, optionally substituted naphthyl, optionally substituted heteroaryl or optionally substituted benzoic fusion heteroaryl, R21, R22 and R23 are independently
priorityDate 1991-07-23-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID13038
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID136721
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID128995187
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID129867253
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID129871639
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID129928649
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID226397584
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID17208
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID232062476
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID226394049
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID73949
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID10965460
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID129664945
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID128840476

Total number of triples: 292.