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filingDate 1996-08-28^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_d8f9457babb6b09abeec2792e580a4d6
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_03de7fd9767d38304010c9bc5fb0197f
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a6b81a0ad27406e49e117abe7354a1e5
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_6e399e5eb8b169a330fe11051d99cfe4
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ba47a025b7af1fb7f8172773c7a1975a
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_5b5f381e66973ff8f3a2f0aefaa532b1
publicationDate 1997-05-13^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-H09124600-A
titleOfInvention Novel piperidine derivatives, methods for obtaining them and pharmaceutical compositions containing them
abstract (57) [Summary] (Modified) [Problem] To provide a piperidine derivative for use in healing in pathological phenomena including tachykinin system. Kind Code: A1 Piperazine derivatives represented by the compounds of formula (I "" a) and formula (I "" b), methods for producing them, and pharmaceutical compositions containing them. [In the formula, A ′ represents a direct bond or —CH 2 —, Z′a Represents a phenyl group which may be substituted with halogen or C 1 -C 10 alkoxy at the 3-position, Z′b represents phenyl, 3,5- or 2,4-bis (trifluoromethyl) phenyl, 3,5 -Represents dimethylphenyl, R 13 , R 17 and R 18 represent a hydrogen atom and C 1 -C 7 alkyl, and R 18 represents C 3 -C 7 cycloalkyl, phenyl, Represents benzyl and the like, q is 0, 1, 2] [Effect] The compound has a neurokinin receptor antagonistic activity, and is useful for healing all substance p- and neurokinin dependences.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-4729259-B2
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2010215666-A
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2005529114-A
priorityDate 1995-08-28^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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