http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-H05279315-A
Outgoing Links
Predicate | Object |
---|---|
classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P37-08 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P43-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P7-04 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P7-02 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C257-18 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P1-04 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P1-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P29-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-235 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-245 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-24 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12N9-99 |
filingDate | 1992-04-01-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationDate | 1993-10-26-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationNumber | JP-H05279315-A |
titleOfInvention | Benzoic acid amidinophenyl ester derivative |
abstract | (57) [Summary] [Purpose] To provide a novel protease inhibitor. [Structure] The following formula (I): (In the formula, R 1 and R 2 are the same or different, A hydroxyl group, an amino group, a halogen atom, a carboxyl group or a 4-amidinophenyl-1-oxycarbonyl group is shown. However, R 1 and R 2 are not a hydrogen atom or a 4-amidinophenyl-1-oxycarbonyl group at the same time, and R 1 and R 2 may be protected. ) The benzoic acid amidinophenyl ester derivative and its acid addition salt. [Effect] The compound of the present invention has inhibitory activity against serine proteases such as trypsin, thrombin and factor Xa at an extremely low concentration. |
isCitedBy | http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-9910316-A1 |
priorityDate | 1992-04-01-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 164.