http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-S5651452-A

Outgoing Links

Predicate Object
assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_1374dd16777534b65ad4422333245af8
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-60
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D209-12
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P29-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P7-02
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P9-08
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-403
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-40
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P9-10
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-404
filingDate 1979-10-03-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_d8f27821fb9224f44007b56410c4f427
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_5fa29223188087f431fd9f445a813c48
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_bc73a53703b5cdb6582ae13ea7614f2c
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_45b45e663ab3ee9bb0604b862f44baa5
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_08cc131ed8a82d49cd5d79f8e408787e
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_1216d44ad651531644e2ea82b190b5c0
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a003e516b0070f4851f6e5ac45810acf
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_5a3e031c2c78c88ee6aed81c1b9b7b78
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_5c247b3bab7eff298cd96066158853b2
publicationDate 1981-05-09-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-S5651452-A
titleOfInvention Derivative of acylated indole, its preparation and blood platelet coagulation suppressing agent containing said compound as effective component
abstract NEW MATERIAL:Derivatives of acylated indole of formula I [R 1 is lower alkyl or (substituted) phenyl; R 2 is H or lower alkyl; R 3 and R 4 are H, halogen, lower alkoxy, lower alkylthio, lower alkylsulfinyl, amino, lower alkyl-substituted amino, trifluoromethyl, etc., or R 3 and R 4 together form methylenedioxy or ethylenedioxy; ϕ is aryl or alicyclic group]. n EXAMPLE: 3-Benzoyl-2-methyl-1-(3-oxo-2-butyl) indole. n USE: Preventive agent for cardiac vascular infarction, preventive and treatment agent for post-operative diseases, antiinflamatory agent, fibrinolytic agent etc. It has excellent activity to suppress the coagulation of blood platelets. n PROCESS: A compound of formula I is obtained by the reaction of e.g. a compound of formula II with a compound of formula III (X is halogen) in the presence of a basic compound. n COPYRIGHT: (C)1981,JPO&Japio
priorityDate 1979-10-03-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

Incoming Links

Predicate Subject
isDiscussedBy http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID457311044
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID70527595
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID458396401
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID56605938
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID70527593
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID798
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID226421593
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID236373428
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID226393662
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID428264975
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID236373432

Total number of triples: 37.