http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-1735312-A1

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filingDate 2005-04-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_047e643db3b6ec6cfcb6e0e228418c30
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f0241976e6cbe7ba1b87bc34e2c72eb1
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_df89ad17efbbbb2caf93ae1dd5fca42a
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b9b443b1808c6503ec03a7f0062c933b
publicationDate 2006-12-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-1735312-A1
titleOfInvention Substituted diaza-spiro-[5.5|-undecane derivatives and their use as neurokinin antagonists
abstract This invention concerns substituted diaza-spiro-[5.5]-undecane derivatives having neurokinin antagonistic activity, in particular NK1 antagonistic activity, a combined NK1/NK2 antagonistic activity, a combined NK1/NK3 antagonistic 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, COPD and micturition disorders such as urinary incontinence. The compounds according to the invention can be represented by general Formula (I) (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: 512.