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filingDate 1986-04-14-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b2e158fb72a2046dc654d02859673fb0
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f06c2fa9853fcf0d38cf89ee0326cf23
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e986b6a3fb8f3413da69071c1facfa87
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_3ee138baa0431bf7218eb993cac29f68
publicationDate 1986-11-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-0202759-A2
titleOfInvention Leukotriene antagonists
abstract Compounds of formula (I) n<CHEM>n in which R1 is C8to C13 alkyl, C7 to C12 alkoxy, C7 to C12 thioalkyl, C10 to C12 1-alkynyl, 10-undecynyloxy, 11-dodecynyl, phenyl-C4 to C10 alkyl, phenyl-C3 to C9 alkoxy, phenylthio-C3 to C9 alkyl with the phenyl optionally mono substituted; R2 is hydrogen, bromo, chloro, methyl, trifluoromethyl, hydroxy, methoxy or nitro; or R1 is hydrogen and R2 is C8 to C13 alkyl, C7 to C12 alkoxy, C7 to C12 thioalkyl, C10 to C12 1-alkynyl, 10-undecynyloxy, 11-dodecynyl, phenyl-C4o to C10 alkyl, phenyl-C3 to C9 alkoxy, phenylthio-C3 to C9 alkyl with the phenyl optionally mono substituted;n Y is COR3, n<CHEM>n or (CH2)0-1-C-tetrazolyl;n R3 is hydroxy or amino; R4 is hydrogen, methyl, methoxy, fluoro or hydroxy; m is 0, 1 or 2;n R is n<CHEM>n, CH(CO2H)CH2CO2H, CH2CH2Z or n<CHEM>n n is 0, 1 or 2; R5 is hydrogen, amino or NHCOCH2CH2CH(NH2)CO2H; R6 is hydroxy, amino or NHCH2CO2H; Z is SO3H, SO2NH2 or CN; R7 is hydrogen, C1 to C4 alkyl or C3 to C4 alkenyl; R8 is hydrogen, C1 to C4 alkyl, carboxyl or carboxamido, or (CH2)pCO2H, in which p is 1 or 2, when R7 and R9 are hydrogen or C1 to C4 alkyl; and R9 is hydrogen, C1 to C4 alkyl or CH2CO2H; compositions containing then and their use in therapy as leukotriene antagonists, for example in the treatment of asthma.
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priorityDate 1985-04-19-04:00^^<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: 874.