http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-0544681-A1

Outgoing Links

Predicate Object
assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_897769c87cd0311c34b3ffc629f7a8dc
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P7-02
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D309-40
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P43-00
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P43-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D309-40
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-35
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P7-02
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12P17-06
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-625
filingDate 1991-06-21-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_1fe29e294bef315364c6bde0d5cec384
publicationDate 1993-06-09-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-0544681-A1
titleOfInvention NEW CONJUGATES OF SALICYLIC ACID AND MALTOL.
abstract New conjugates of salicylic acid and maltol corresponding to formula (I), in which R represents H, C1-5 alkyl groups or C1-5 alkanoyl groups, and R1 represents H or C1-5 alkyl groups. The new maltol esters of salicylic acid derivatives have more powerful antioxidant and antithrombotic activities than those of salicylic acid derivatives.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-8406302-B2
priorityDate 1991-06-21-04:00^^<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/CID31113
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID19906651
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID129287822
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID129627858
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID226396740
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID129720848
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID128331689
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID8369
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID16639
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID3073200
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID226410237
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID227428161
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID338
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID226395769
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID6335613
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID4277
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID10899264
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID2244
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID226394110
http://rdf.ncbi.nlm.nih.gov/pubchem/taxonomy/TAXID4054
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID226395791
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID128931013
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID272730
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID197341
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID11370
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID226400117
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID228304246
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID10868
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCP84122
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID10964
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID4781
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID234911571
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID226393392
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID127389669
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID226395115
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID62020
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID1268265
http://rdf.ncbi.nlm.nih.gov/pubchem/anatomy/ANATOMYID4054
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID226394558
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID128186503
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID226412196

Total number of triples: 60.