http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-2002161012-A1

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_0be8d6cfb14d04522568dd6146ad713a
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D261-18
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D261-18
filingDate 2002-01-17-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e09c7d55446c47f338b502233a094081
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_52336e4450891e248a503f629ce9eee3
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_17f4a2b5fed5c1e0117a828aba01c8c0
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b69dacdab0febffa81324bcde848acbb
publicationDate 2002-10-31-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-2002161012-A1
titleOfInvention Isoxazolecarboxamide derivatives
abstract The invention relates to novel N-(substituted phenyl)-N′-[(ω-(3-substituted phenyl-4-isoxazolecarbonylamino)alkyl]piperazines, their N-oxides, and pharmaceutically acceptable salts thereof. The compounds are endowed with enhanced selectivity for alpha1-adrenergic receptors and a low activity in lowering blood pressure. The compounds are useful in the treatment of obstructive syndromes of the lower urinary tract, including benign prostatic hyperplasia (BPH), and in the treatment of lower urinary tract symptoms (LUTS) and neurogenic lower urinary tract dysfunction (NLUTD), and other conditions. The compounds may be administered alone or in combination with an anticholinergic compound.
priorityDate 1999-10-18-04:00^^<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: 773.