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filingDate 1996-01-08-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_067edc01f01af67f6dd7966049f34d02
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_4697bbde0e00f404a2d8201ef27806f4
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_be3ba066698b3e40c934d071c7b1e86c
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_62b5bc28abd1f2fd3a683854ad524dda
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_6cc611197a87d1156315572ae3e397ba
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_622472e980516272eb8c17165ec79b5c
publicationDate 1998-02-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber SK-93297-A3
titleOfInvention Indole derivatives, method for their producing, pharmaceutical comosition containing the same, and their use
abstract A compound of formula (I) or a salt thereof, or a solvate thereof, wherein either: (i) Ra represents a group R5 which is hydrogen, alkyl or optionally substituted aryl and Rb represents a moiety of formula (a); wherein X represents a hydroxy or an alkoxy group wherein the alkyl group may be substituted or unsubstituted or X represents a group NRsRt wherein Rs and Rt each independently represent hydrogen, alkyl, substituted alkyl, optionally substituted alkenyl, optionally substituted aryl, optionally substituted arylalkyl, an optionally substituted heterocyclic group or an optionally substituted heterocyclylalkyl group, or Rs and Rt together may form a heterocyclic group; R1 represents an alkyl or a substituted or unsubstituted aryl group; and R2, R3 and R4 each independently represent hydrogen, alkyl, aryl or substituted aryl or (ii) Ra represents a moiety of the above defined formula (a) and Rb represents the above defined R5; R6 and R7 each independently represents hydrogen, hydroxy, amino, alkoxy, optionally substituted aryloxy, optionally substituted benzyloxy, alkylamino, dialkylamino, halo, trifluoromethyl, trifluoromethoxy, nitro, alkyl, carboxy, carbalkoxy, carbamoyl, alkylcarbamoyl, or R6 and R7 together represent methylenedioxy, carbonyldioxy or carbonyldiamino; and R8 represents hydrogen, hydroxy, alkanoyl, alkyl, aminoalkyl, hydroxyalkyl, carboxyalkyl, carbalkoxyalkyl, carbamoyl or aminosulphonyl; a process for the preparation of such a compound, a pharmaceutical composition comprising such a compound and the use of such a compound in medicine.
priorityDate 1995-01-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID57517941
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID421753557
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID86725019
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID421474531
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID54051711
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID10806018
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID70139389
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID421474532
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID415750740
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID14358692
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID458394811
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID20722760
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID2724682
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID149436139
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID75051
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419521903
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID421474401
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID421110030
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID426476737
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID19610413
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID421474542
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID414803645
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID522220
http://rdf.ncbi.nlm.nih.gov/pubchem/anatomy/ANATOMYID12721
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID9833941
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID70670
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID22180045
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID19610404
http://rdf.ncbi.nlm.nih.gov/pubchem/taxonomy/TAXID11276
http://rdf.ncbi.nlm.nih.gov/pubchem/anatomy/ANATOMYID11276
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID6436223
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID159087
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419505939
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID19610408
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID410596662
http://rdf.ncbi.nlm.nih.gov/pubchem/taxonomy/TAXID11320
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID19610409
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID22397576
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419535600
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID62034
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID263
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID12159
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID26998

Total number of triples: 331.