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filingDate 2001-01-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2005-10-25-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_273fe7941cbd2744bb5b11450b69259e
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_28a67dc40951de9bda8237a40cdebff5
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_22cd448cc00fe2412e1ac70499c0ca3c
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_00d36a05b6204d15f01ee3bc478c7b6c
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a8ba90b678daf2885632564fb0b9084c
publicationDate 2005-10-25-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CA-2332461-C
titleOfInvention New benzenesulfonamide derivatives, their method of preparation and the pharmaceutical compositions containing them
abstract The invention relates to novel compounds of formula (I) wherein n is an integer inclusive of 1 to 3; m is a whole included inclusively between 0 and 6; Ra represents a hydroxy group, a C1-C6 alkoxy group C6, aryloxy or arylalkyloxy; R1 and R2 independently represent a hydrogen atom or halogen, or an alkyl, C 1 -C 6 alkoxy, hydroxy or perhaloalkyl C1-C6 alkyl; R3 represents a hydrogen atom or an alkyl, arylalkyl group, cycloalkylalkyl, aryl or cycloalkyl; T1 represents an alkylene group, O-alkylene, alkylene-O- or alkylene-O-alkylene in which the alkylene groups behave each 1 to 3 carbon atoms; and G represents a group G1- or G1-T2-A-, in which A represents an aryl group, T2 represents a bond or a group alkylene, O-alkylene, alkylene-O- or alkylene-O-alkylene in which the groups alkylene each have 1 to 3 carbon atoms, G 1 represents a group -NR4R5, wherein R4 and R5 independently represent a hydrogen atom or one alkyl, cycloalkyl, aryl, arylalkyl, cycloalkylalkyl, heteroaryl or optionally substituted heteroarylalkyl, or else G1 represents a group heterocycloalkyl of formula having 5 to 7 members, wherein Y represent a nitrogen or oxygen atom, or a group CH or CH2 and R6 represents a atom hydrogen or an alkyl, cycloalkyl, cycloalkylalkyl or aryl group, arylalkyl, arylcarbonyl, arylcarbonylalkyl, diarylalkyl, diarylalkenyl, (Aryl) (hydroxy) alkyl, heteroaryl, heteroarylalkyl, heteroarylcarbonyl, or hétéroarylcarbonylalkyle. The invention also relates to the enantiomers and diastereoisomers of the compounds Formula (I), and their addition salts with an acid or a base pharmaceutically acceptable. The compounds according to the invention are useful for the manufacture of medicaments destined for to be used as TXA2 receptor antagonists and HT2, or used in the treatment of atherosclerotic cardiovascular thrombotic asthma, pinprasas, migraine or venous diseases.
priorityDate 2000-01-19-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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