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filingDate 1992-02-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_2f8bfd7aaaa8a3d2f43925eafd107f4a
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publicationDate 1993-04-16-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-H0592954-A
titleOfInvention Cycloalkano [1,2-b indolesulfonamide and method for producing the same
abstract (57) [Summary] (Modified) [Structure] Expression [Wherein R 1 is H, F, CF 3 , —COOR a (R a = H, alkyl), - S (O) m R 3 (R 3 = H, alkyl, aryl; m = 0,1,2), - NR 4 R 5 (R 4, R 5 = H, alkyl, aryl, aralkyl), - OR 6 (R 6 = H, alkyl, aryl, aralkyl, alkyl -SO 2 -, aryl -SO 2 -, Aralkyl -SO 2 -, CF 3, etc.); R 2 is F, C N, CF 3, CF 3 O , R b O (R b = alkyl, phenyl, benzyl); - NR 4 R 5 ( R 4, R 5 = above); x is a number of 1, 2, 3; y is Represents the number 0, 1] Of benzenesulfonamide alkyl] cycloalkano [1,2-b] indole and its preparation by condensation of phenylhydrazine with cycloalkane-benzenesulfonamide. [Effect] This compound is converted to a novel compound having a platelet aggregation inhibitory action by 2-carboxyethylation of indole-N.
priorityDate 1986-02-21-04:00^^<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/substance/SID426004119
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID77857
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID23712863
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID11958046
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID415730448
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID9588
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID458393677
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID20073554
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID14441149
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID458393684
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID450662553
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID87457779
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID416014513
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID458393644
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID14130441

Total number of triples: 312.