http://rdf.ncbi.nlm.nih.gov/pubchem/patent/PE-20110205-A1

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filingDate 2009-08-03-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ebbf482521f36e2c6919a7433ac5b45a
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publicationDate 2011-04-07-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber PE-20110205-A1
titleOfInvention N-BENCENSULFONAMIDE-3,4-DIAMINO-3-CYCLOBUTENE-1,2-DIONE DERIVATIVES SUBSTITUTED AS ANTAGONISTS OF THE CXCR2 CHEMOKIN RECEPTOR
abstract REFERS TO COMPOUNDS DERIVED FROM BENZEN-SULFONAMIDE OF FORMULA (I) WHERE R1 IS H, CARBOCYCLIC (C3-C10), ALKYL (C1-C6) OPTIONALLY SUBSTITUTED WITH HALOGEN, CN OR OH, AMONG OTHERS; R2 IS CARBOCYCLIC (C3-C10), ALKYL (C1-C6), OPTIONALLY SUBSTITUTED ALCOXYL (C1-C6), AMONG OTHERS; R3 IS H, HALOGEN OR CN; R4 IS H, ALKYL (C1-C8), CYCLOALKYL (C3-C8), AMONG OTHERS; R5 IS ALKYL (C1-C8), CYCLOALKYL (C3-C8), CYCLOALKENYL (C5-C8), AMONG OTHERS; X IS CR14 O N, WHERE R14 IS H O ALKYL (C1-C6). PREFERRED COMPOUNDS ARE: 6-CHLORO-3- [3,4-DIOXO-2 - ((R) -1-PHENYL-PROPYL-AMINO) -CYCLOBUT-1-ENYL-AMINO] -2-HYDROXY-N-METOXY- N-METHYL-BENZEN-SULFONAMIDE, 6-CHLORO-2-HYDROXY-N-METOXY-N-METHYL-3- {2 - [(R) -1- (5-METHYL-FURAN-2-IL) -PROPIL- AMINO] -3,4-DIOXO-CYCLOBUT-1-ENYL-AMINO} -BENCEN-SULFONAMIDE, 6-CHLORO-3- {3,4-DIOXO-2 - [(S) - (TETRAHYDRO-THIOFEN-3-IL ) -AMINO] -CYCLOBUT-1-ENYL-AMINO} -2-HYDROXY-N-METOXY-N-METHYL-BENZEN-SULFONAMIDE, AMONG OTHERS. IT ALSO REFERS TO A PREPARATION PROCEDURE. SUCH COMPOUNDS ARE ANTAGONISTS OF THE CXCR2 CHEMOKIN RECEPTOR, BEING USEFUL IN THE TREATMENT OF CHRONIC PULMONARY OBSTRUCTIVE DISEASE, EMPHYSEMA, OVARY CANCER, PULMONARY FIBROSIS
priorityDate 2008-08-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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