http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-H03232870-A

Outgoing Links

Predicate Object
assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_400cd24db1653476b271d31812b8817c
http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_44c713790ce00813da2e6c6d57a29456
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-145
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C333-32
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-535
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D265-30
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-5375
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P1-16
filingDate 1990-02-06-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_149702e9b8d257d91c90b0f867932a38
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_8650e29fa662ff8d85b7f44fbe6d6ae3
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_001b641ffb81ebbbdfca01f9896dadcc
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_261ed6722c889448ff43de456947ff62
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ac2af401aaa4a905fb917d76c96ba79d
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b0f147195de64fe9894f4ef9f11eead5
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e9dc55a35fba32a36432d66761a4dacc
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_429e6380a930fa49d8cd6954313923b1
publicationDate 1991-10-16-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-H03232870-A
titleOfInvention Thioamide compound
abstract NEW MATERIAL:2,6-Dimethylmorpholino-N-phenylthiourea shown by formula I and N,N'-dimethyl-N,N'-bis(m-tolyl)thiuram disulfide shown by formula II. n USE: A therapeutic agent for liver diseases. n PREPARATION: 2,6-Dimethylmorpholine is made to react with phenyl isothiocyanate is a solvent such as toluene at room temperature to the boiling point of the solvent to give a compound shown by formula I. The compound shown by formula II is obtained by reacting N-methyl-m-toluidine with carbon disulfide and an aqueous solution of an alkali such as sodium hydroxide to give sodium N-methyl-N-(m-tolyl)dithiocarbamate, which is then oxidized with sodium hypochlorite at 20-50°C. n COPYRIGHT: (C)1991,JPO&Japio
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-2214709-A4
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-103012226-A
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2002537377-A
priorityDate 1990-02-06-04:00^^<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/SID226414710
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID6348
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID408460211
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID452802464
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID23665760
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID15020868
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID453313435
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID110862
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID226452055
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID226646054
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID409060395
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID7673
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID69675
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID226410347
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID235139608
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID1140
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID426703316
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID235139578
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID14798
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419559234
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID88513063
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID420926252
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID456922693
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID2761171
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419516421

Total number of triples: 51.