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filingDate 1992-07-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_02392400ff05f3596e85bd9cc7ab2b21
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_15b16bf0b25af68e35b4e1a029b4edbf
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_86d7c391dd365b66d0d1574c939cfcc2
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_8279ce11c4fb389bdb96a8667d01361d
publicationDate 1993-02-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber IE-922465-A1
titleOfInvention 2-(imidazol-1-yl)-2-benzylethylidene-aminoxyalkanoic acid¹ derivatives
abstract The present invention relates to 2-(imidazol-1-yl)-2-benzylethylidene-aminoxyalkanoic acids and esters thereof of formula (I) wherein A is a divalent group of formula in which R is hydrogen, halogen, CF3, C1-C4 alkoxy, C1-C4 alkylsulfonyl or cyano; R1 is a) phenyl unsubstituted or substituted by halogen, C1-C4 alkoxy, CF3 or C1-C4 alkylsulfonyl; b) cyclohexyl; or c) a straight or branched C1-C6 alkyl group; T is a branched or straight C3-C5 alkylene chain; R2 is hydrogen or C1-C4 alkyl, and the pharmaceutically acceptable salts thereof, which are useful as selective inhibitors of thromboxane A2 (TxA2) synthesis.
priorityDate 1991-07-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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