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filingDate 2007-12-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e174bb6487cb193d4daef26032c9f3d1
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_9af0519cfb7a900b2e88814746a29279
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e11686d416f9daa169b7d38b80a42394
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c7f400e90cf5bf934360673256aa2cb0
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_7af10e3cd8f0411ca867714381648c75
publicationDate 2008-04-03-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-2008074875-A
titleOfInvention Sulfonamides for the treatment of endothelin-mediated disorders
abstract The vascular endothelium releases various vasoactive substances such as endothelin (ET), which is a vasoconstrictive peptide derived from the endothelium. Thienyl-, furyl- and pyrrolyl-sulfonamides; pharmaceutically acceptable salts of sulfonamides; salts and formulations of the sulfonamides; and endothelin peptides using the formulations and sulfonamides Methods of modulating or altering the activity of are provided. Specifically, formulations of sodium salts of N- (isoxazolyl) thienylsulfonamides, N- (isoxazolyl) furylsulfonamides and N- (isoxazolyl) pyrrolylsulfonamides are provided. A process for the production of an alkali metal salt of a hydrophobic sulfonamide is provided. The method includes dissolving a free sulfonamide in an organic solvent in the presence of a saturated alkali metal salt solution and recovering the produced sulfonamide salt from the organic solvent. [Selection figure] None
priorityDate 1997-04-28-04:00^^<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: 917.