http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-S59164768-A

Outgoing Links

Predicate Object
assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_e7962109cd4763907b82b66760cd0ae8
classificationCPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/Y02P20-52
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/B01J27-10
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P9-12
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C325-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/B01J27-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/B01J31-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/B01J31-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07B61-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C67-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C337-08
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-175
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12N9-99
filingDate 1983-03-11-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_504be0d0477262470ee334aafdeefe58
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a64a5b8ff274af8d52b695d57fc269d7
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_fa0747a699d08c7913d2532734a45aab
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_05d9fd4e83117ef849c16c47df71b742
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_91bf4366d4ae7df449a7fb940be84364
publicationDate 1984-09-17-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-S59164768-A
titleOfInvention Thiosemicarbazone and its preparation
abstract NEW MATERIAL:A compound shown by the formula I (X is H, halogen, lower alkyl, lower alkoxy, phenyl, or phenoxy; R is lower alkyl, or 3,4-dihydroxystyryl). n EXAMPLE: 1-(4-Methylphenyl)butan-1-onethiosemicarbazone. n USE: A hypotensor. Having an inhibitory action on decarboxylase. The use of it together with dopa in Parkinson's disease enhances the effect of dopa. n PREPARATION: A ketone shown by the formula II is reacted with thiosemicarbazide in a solvent such as methanol, ethanol, etc. in the presence of an acid catalyst (e.g., acetic acid, hydrochloric acid, etc.) at 40W70°C for 2W24hr to give a compound shown by the formula I . n COPYRIGHT: (C)1984,JPO&Japio
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-8904824-A1
priorityDate 1983-03-11-04:00^^<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/compound/CID836
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID226412729
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419536281
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID406903350
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419538410
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID176
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID6047
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID410444215
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID702
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID71407464
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID458394811
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419492817
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID5370664
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID428409669
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419557048
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID887
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID2723789
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID226532310
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID411932836
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID226411642
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID313
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID458394858
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID236265068
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID151398

Total number of triples: 50.