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filingDate 2005-04-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2010-06-23-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_6b6840df5b4ba406a4c95e808b8da04a
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_134d0302d0b7f4e1efb98f7b5632c393
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_2730eb4d055f672c506c6ca33137d3f9
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_df89ad17efbbbb2caf93ae1dd5fca42a
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b764a58282c2cd646bcd0825d75210f0
publicationDate 2010-06-23-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-1735313-B1
titleOfInvention Substituted diaza-spiro-[4.5]-decane derivatives and their use as neurokinin antagonists
abstract This invention concerns substituted diaza-spiro-[4.5]-decane derivatives having neurokinin antagonistic activity, in particular NK1 antagonistic activity, a combined NK1/NK2 antagonist ic activity, a combined NK1/NK3 antagonist ic activity and a combined NK1/NK2/NK3 antagonistic activity, their preparation, compositions comprising them and their use as a medicine, in particular for the treatment and/or prophylaxis of schizophrenia, emesis, anxiety and depression, irritable bowel syndrome (IBS), circadian rhythm disturbances, pre-eclampsia, nociception, pain, in particular visceral and neuropathic pain, pancreatitis, neurogenic inflammation, asthma, chronic obstructive pulmonary disease (COPD) and micturition disorders such as urinary incontinence. The compounds according to the invention can be represented by general Formula (I) and comprises also the pharmaceutically acceptable acid or base addition salts thereof, the stereochemically isomeric forms thereof, the N-oxide form thereof and prodrugs thereof, wherein all substituents are defined as in Claim 1.
priorityDate 2004-04-06-04:00^^<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: 531.