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filingDate 1998-06-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_75cc35ed92bb3647576b5086a76be295
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_2636b655600cd11fc5257e5c6f2d205f
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_fd980ab0b758627986379937b983aeae
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c20f00656ba786718e0ac7fc18a7d7ec
publicationDate 1999-05-06-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-0887346-A3
titleOfInvention Phenyl-and aminophenyl-alkylsulfonamide and urea derivatives, their preparation and their use as alpha1A/1L adrenoceptor agonists
abstract The present invention concerns novel compounds represented by thenFormula:n nwherein: A is R 1 q (R 3 R 60 N) m (Z)(NR 2 ) n ; m and q are each 0 or 1, with the proviso thatnwhen q is 1, m is 0 and when q is 0, m is 1; Z is C=O or SO 2 ; n is 1 with the provisonthat, when Z is C=O, m is 1; X is -NH-, -CH 2 -, or -OCH 2 -; Y is 2-imidazoline,n2-oxazoline,n2-thiazoline, or 4-imidazole; R 1 is H, lower alkyl, or phenyl, with the provisonthat, when R 1 is H, m is 1; R 2 , R 3 , R 60 are each independently H, lower alkyl, ornphenyl; R 4 , R 5 , R 6 , and R 7 are each independently hydrogen, lower alkyl, -nCF 3 , lowernalkoxy, halogen, phenyl, lower alkeny, hydroxyl, lower alkylsulfonamido, or lowerncycloalkyl, wherein R 2 and R 7 optionally may be taken together to form alkylene ornalkenylene of 2 to 3 atoms in an unsubstituted or optionally substituted 5-orn6-memberednring, wherein the optional substituents on the ring are halo, lower alkyl, orn-CN, with the proviso that, when R 7 is hydroxyl or lower alkylsulfonamido, then X isnnot -NH- when Y is 2-imidazoline. The compounds include pharmaceuticallynacceptable salts of the above. In the above formula A may be, for example,n(R 1 SO 2 NR 2 -), (R 3 R 60 NSO 2 NR 2 -), or (R 3 R 60 NCONR 2 -). The invention also includes thenuse of the above compounds, and compositions containing them, as alpha 1A/1L nagonists in the treatment of various disease states such as urinary incontinence,nnasal congestion, priapism, depression, anxiety, dementia, senility, Alzheimer's,ndeficiencies in attentiveness and cognition, and eating disorders such as obesity,nbulimia, and anorexia.
priorityDate 1997-06-23-04:00^^<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: 562.