http://rdf.ncbi.nlm.nih.gov/pubchem/patent/MX-PA06011683-A

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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_26ed63498df2f132abcd2844e74e774d
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_df89ad17efbbbb2caf93ae1dd5fca42a
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_7220e6be8c29c020fed0711921c25c91
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_71ea97029e5292e3a31678648b0964bd
publicationDate 2006-12-14-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber MX-PA06011683-A
titleOfInvention DERIVATIVES OF 4-ALQUIL- AND 4-ALCANOIL-PIPERIDINA SUBSTITUTED AND ITS USE AS AN ANTHOGONIST OF NEUROQUININS.
abstract The present invention describes substituted 4-alkyl- and 4-alkanoyl-piperidine derivatives having neuroquinine antagonist activity, in particular, NK1 antagonist activity and NK1 / NK3 combined antagonist activity; with compositions comprising said derivatives and with their use as a medicament, especially for the treatment or prophylaxis of schizophrenia; the vomit; anxiety and depression; irritable bowel syndrome (IBS), circadian rhythm disturbances; preeclamsia; nociception; pain, in particular, visceral and neuropathic pain; pancreatitis; neurogenic inflammation; asthma; chronic obstructive pulmonary disease (COPD), and urination disorders, such as urinary incontinence; The compounds according to the invention can be represented by the general Formula (I): (see formula (I)) and also comprise their pharmaceutically acceptable base or acid addition salts; its stereochemically isomeric forms; its N-oxide form; and its prodrugs, wherein all substituents are defined in accordance with claim 1.
priorityDate 2004-04-08-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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