http://rdf.ncbi.nlm.nih.gov/pubchem/patent/UY-24507-A1
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_ec35c5a8f37161e7faef708491127d1d |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P35-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P29-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P19-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P7-02 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D211-58 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C211-46 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C235-54 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-445 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C253-02 |
| filingDate | 1997-04-01-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b11948bd0ac3006e6452762892eeea13 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_912c7a6cbe63e92f128019d882b0e230 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_9ffdd47cddddc654cb28d966633ce69d http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b2983ba1abc315d73f74f2c21f592261 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_48465624ec8764fc1e27eec9007f3830 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a24e922395ae54e102ad9bf093124c4d |
| publicationDate | 1997-09-22-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | UY-24507-A1 |
| titleOfInvention | PROCEDURE FOR THE PREPARATION OF CARBOXYL ACID DERIVATIVES AND MEDICINES CONTAINING THEM |
| abstract | The present invention concerns a process for the preparation of derivatives of carboxylic acids of general formula (I) (FIGURE 1), in which X1, X2 and X3, which may be the same or different, in each case represent a nitrogen atom or a methine group, in which, in heterocyclic rings, in which X2 or X3 or X2 and X3 each represent a nitrogen atom, additionally in each case a methylene group, linked to a nitrogen atom of the ring, can be replaced by a carbonyl group; B signifies a 3-piperidinylene, 4-piperidinylene or 1,4-piperazinylene group, in which in each case a methylene group adjacent to a nitrogen atom can be replaced by a carbonyl group; their tautomers, their stereoisomers, including their mixtures, and their salts. These compounds have valuable pharmacological properties, such as: inflammation inhibiting effect and bone degradation inhibitor, antithrombotic and antiaggregative effects and tumor or metastasis inhibitors. Non-limiting example: 1- (4-carboxymethyloxy-phenyl) -4- [2- (piperidin-4-yl) -ethyl] -piperazine. |
| priorityDate | 1996-04-10-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 29.