http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CA-2132792-A1

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filingDate 1994-09-23-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_988dadb47314ba4a045dd28851b0be3b
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_8add3d291c380ba92257b848c637b68a
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_5b28e1bd1e8fce6be24c1353f429b9e4
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_4c5c7dc237c167b4b2026a8af2326763
publicationDate 1995-03-25-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CA-2132792-A1
titleOfInvention Condensed cyclic compounds and their use
abstract Abstract of the disclosure Disclosed is a squalene synthetase inhibitor which comprises the compound represented by the formula wherein R1 is hydrogen or an optionally substituted hydrocarbon group; R2 is hydrogen, an optionally substituted alkyl group, an optionally substituted phenyl group or an optionally substituted aromatic heterocyclic ring group; X' is a substituent comprising an optionally esterified carboxyl group, an optionally substituted carbamoyl group, an optionally substituted hydroxyl group, an optionally substituted amino group or an optionally substituted heterocyclic radical having a protonizable hydrogen; Ring A is an optionally substituted benzene ring or an optionally substituted aromatic heterocyclic ring; Ring J' is a 7- to 8-membered heterocyclic ring containing at most three ring constituting hetero atoms; D is C or N; the Ring J' optionally having, besides R1, R2 and X', a further substituent; provided that the condensed ring composed of Ring A and ring J' is not a 2-oxo-1,2,3,5-tetrahydro-4,1-benzoxazepine ring, or a pharmaceutically acceptable salt thereof, and which is useful for the prophylaxis or therapy of hypercholesteremia or coronary sclerosis of mammals.
priorityDate 1993-09-24-04:00^^<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: 417.