http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-H08311043-A

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filingDate 1995-05-16-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_2aedd16109e96e98a1cc5ea1df01e8b6
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_406c0d2d5f27baa0e84defe572b744fc
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publicationDate 1996-11-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-H08311043-A
titleOfInvention Sulfonamide derivative
abstract (57) [Summary] [Structure] General formula [I] (However, Ring A represents a substituted or unsubstituted monocyclic or bi- to tricyclic hydrocarbon group or a substituted or unsubstituted heterocyclic group, and Ring B is (1) Ring A is a substituted or unsubstituted monocyclic group. In the case of a cyclic hydrocarbon group, a substituted or unsubstituted di- to tricyclic hydrocarbon group or a substituted or unsubstituted heterocyclic group, (2) When ring A is a substituted or unsubstituted bi- to tricyclic hydrocarbon group or a substituted or unsubstituted heterocyclic group, a substituted or unsubstituted monocyclic or bi- to tricyclic hydrocarbon group or substituted or Represents an unsubstituted heterocyclic group, and Q is of the formula- O is a group represented by O-, Y is a group represented by the formula -O-, A lk is a lower alkylene group or the like, Z is a group represented by the formula —O—, R is a substituted or unsubstituted aromatic heterocyclic group, R 1 represents a hydrogen atom or the like. ) A sulfonamide derivative represented by or a pharmaceutically acceptable salt thereof. [Effect] This compound exhibits excellent endothelin antagonism.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-4769460-B2
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priorityDate 1995-05-16-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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