http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2002088081-A

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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P1-00
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filingDate 2000-09-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_681a59838483700a8d73ded90d20458c
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_248aeca7d79fec041c3500605bc085f2
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publicationDate 2002-03-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-2002088081-A
titleOfInvention Novel naphthyridine derivative or pharmacologically acceptable salt thereof
abstract (57) [Summary] [PROBLEMS] A novel tachykinin receptor antagonist is desired. A novel naphthyridine derivative represented by the following general formula (1) or a pharmacologically acceptable salt thereof is provided. Embedded image For example, in the formula, R1, R2, R3, R4, R5, R6 and R7 each independently represent a hydrogen atom, a lower alkyl group, a hydroxyl group, It represents a lower alkoxy group or a lower acyloxy group. Q is N An amino-protected compound represented by RaCORb; L is an unsubstituted or oxygen atom; X and Y are ethylene and methylene groups; and Z is a phenyl group or a substituted phenyl group. A represents a hydrogen atom, a lower alkyl group, or the like. G represents an acyl group. As a specific example, 10-acetylamino-2-[(4- (N-benzoyl-N-methyl) amino-3- (3,4-dichlorophenyl) butyl]- 1,2,3,4-tetrahydro-benzo [b] [1, 6] naphthyridine 5-oxide.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2011116867-A1
priorityDate 2000-09-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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