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filingDate 1990-08-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_624cba60b78ff7b6e85c9aceaa2e3d95
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publicationDate 1991-04-11-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-H0386882-A
titleOfInvention Pyrroloquinoline compound
abstract NEW MATERIAL:A compound expressed by formula I {R 1 and R 2 are H or lower alkyl; R 3 is (substituted) aryl or heterocyclic ring; R 4 is H, halogen or lower alkyl; A is methylene, methine, oxa, thia, sulfinyl or sulfonyl; Y is vinylene or ethylene; Z is expressed by formula II or formula III [R 5 is (protected) carboxy; R 6 is H or OH protecting group]; dotted line is single bond or double bond}. n EXAMPLE: (±)-Erythro-(E)-7-[5,6-dihydro-4,4-dimethyl-1-(4-fluorophenyl)-4H- pyrrolo[3,2,1-ij]quinoline-2-yl]-3,5-dihydroxyhepto-6-enic acid. n USE: Inhibitor of 3-hydroxy-3-methylglutaryl.coenzyme-A reductase. n PREPARATION: A compound expressed by formula IV or salt of said compound is reduced to afford a compound expressed by formula V. n COPYRIGHT: (C)1991,JPO&Japio
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priorityDate 1989-08-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
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