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filingDate 1985-10-31-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_67fd015f9ca7622cd4d4eaef75f41baf
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a92b63a352b3bd4ba9043bae3a63c40e
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_4f1dcb078493715111bf7f54ca0c2004
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_9bbff2e786eaf3c115e76b5c421e8eb8
publicationDate 1986-05-14-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-0181163-A2
titleOfInvention Heterocyclic phenoxy derivatives having an antihistamine H2 activity
abstract Compounds of the formula (I) : n<CHEM>n or pharmaceutically acceptable salts thereof, wherein : n<??>R<1> and R<2> are independently C1-4alkyl; or R<1> and R<2> together with the nitrogen atom to which they are joined represent a pyrrolidino, piperidino or hexahydroazepino ring; Y is straight-chain or branched-chain C1-4alkyl; n is 2 to 5; m is 0 or 1; when m is 1, Z is inter alia an optionally substituted pyridine, pyrimidine, oxazole, thiazole, imidazole, benzoxazole benzthiazole or N-alkylbenzimidazole ring; when m is 0, Z is an optionally substituted imidazole, pyrazole or benzimidazole ring. n<??>The compounds are histamine H2-receptors antagonists and relatively lipophilic and can penetrate the blood-brain barrier and are useful in treating diseases mediated via histamine H2- receptors. Processes for their preparation, pharmaceutical compositions and methods of use are described.
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priorityDate 1984-11-03-04:00^^<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: 575.