http://rdf.ncbi.nlm.nih.gov/pubchem/patent/MX-2007001137-A

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filingDate 2005-07-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_54e62c06ae29d5593027bff747761a99
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ee1302f64fcca2ea3f72bd8aa3b6e42b
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e61715394e24c5fc00bf93397ec004b7
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b6f8fe61539ec035bf894e96363dd470
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_7c9f67a1d56e997ac39942b8ae8a5666
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b92807627403077eafa6417ba703d87c
publicationDate 2007-04-19-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber MX-2007001137-A
titleOfInvention DERIVATIVES OF AMINOPIPERIDINE, PREPARATION OF THE SAME AND USE OF THE SAME AS MELANOCORTIN RECEPTOR AGONISTS.
abstract The invention relates to amino-piperidine derivatives of the general formula (I) in which: Ra, Ra 'and R5 represent hydrogen atoms, or alkyl groups, R1 represents a hydrogen atom or an alkyl, cycloalkyl, heterocycloalkyl group or aryl, R2 represents a group of the formulas - (CH2) x- (CO) yY or - (CO) and- (CH2) xY, in which Y represents a hydrogen atom or a hydroxy, alkyl, cycloalkyl group, alkoxy, aryl, heteroaryl or -NR11R12, and being different from a hydrogen atom where x = y = 0, R3 represents 1 to 3 groups chosen from halogen atoms and alkyl, cycloalkyl, -OR, -NRR 'groups, -NR-CO-R ', -NR-CO-NRR', -NR-COOR ', -NO2, -CN and -COOR, and R4 is chosen from the groups of formulas (a), (b) and ( c), in which p = 0, 1, 2 or 3, m = 0, 1 or 2, and X represents an oxygen or sulfur atom or a chain -C (R6) (R7) - or -N ( R10) - :( Formulas (a), (b), (c)). Method of preparation and application in therapy.
priorityDate 2004-07-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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