http://rdf.ncbi.nlm.nih.gov/pubchem/patent/AP-877-A

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D215-48
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D215-48
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P25-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P43-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-47
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-5355
filingDate 1997-08-14-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2000-09-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_39d0b9e7f813f0933a58d695c0673d36
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_3c87f06f52bf03f07e0515b5c9325635
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f7cfafc6813298ca18003f1683f8c754
publicationDate 2000-09-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber AP-877-A
titleOfInvention Tetrahydroquinoline derivatives as EAA antagonists.
abstract Compounds of formula (I) or a salt, or metabolically labile ester thereof wherein R represents a group selected from halogen, alkyl, alkoxy, amino, alkylamino, dialkylamino, hydroxy, trifluoromethyl, trifiuoromethoxy, nitro, cyano, SOhRz or COR2 wherein R2 represents hydroxy, methoxy, amino, alkylamino or dialkylamino; m is zero or an integer 1 or 2; Ri represents a group (CH2)nCN, -CH=CHR3, CH2nNHCOCH2R4 or 0(CH2)pNR5R6; RS represents cyano or the g\ COR7 R4 represents alkoxy or a group NHCORs; Rs and RS 'each represent independently hydrogen or alkyl, or RS and Rg together with the nitrogen atom to which they are attached represent a heterocyclic group, or RS is hydrogen and R6 is the group CORg; RT represents an alkoxy, amino or hydroxyl group; Rs represents a hydrogen atom or optionally substituted alkyl, alkoxy, aryl or heterocyclic group; R9 is the group RS or the group NRioRn wherein RIO represents hydrogen or alkyl group; Rn represents optionally substituted alkyl. aryl, heterocyclic or cycloalkyl group; n is zero or an integer from I to 4; p is an integer from 2 to 4, processes for their preparation and to their use in medicine.
priorityDate 1996-08-17-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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