http://rdf.ncbi.nlm.nih.gov/pubchem/patent/ES-2401936-T3
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_eccd894c99fea2d1c0c8735872bb2309 |
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D495-04 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P17-02 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P25-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P25-28 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P31-18 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P35-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P35-02 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P9-10 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D495-04 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-4365 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P35-02 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P35-00 |
| filingDate | 2008-09-19-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| grantDate | 2013-04-25-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c7f5f50361f2be0b5ca3a1d2ed9dca33 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_4ca2a41f81ab8f70cda0070b001b73a0 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_03798399ef15c00228e2826c00ae8f64 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_d755463cdeb7a4ba3d9f9d402388ae26 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b5fe986c4885b4a84f2a98fcbe46c547 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_89ba1f43c1dbdc4ed30f3aba5dc29f68 |
| publicationDate | 2013-04-25-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | ES-2401936-T3 |
| titleOfInvention | 5-Cyano-thienopyridines for the treatment of tumors |
| abstract | Compounds of the formula I where R1 signifies Het R2, R3 each signifies, independently of one another, H, A, AlkNH2, AlkNHA, AlkNAA ', AlkNHSO2A, AlkOH, AlkOA, AlkCic, AlkCicAlkOH, AlkCicAlkOA, AlkCicAlkCOOAC, AlkCicAlkCOOAC, AlkCicAlkCOOAC, AlkCicAlkCOOAC, AlkCicAlkCOOAC, AlkCicAlkCOOAC, AlkCicAlkCOOAC, AlkCicAlkCOOA, AlkCicAlkCOOAC, AlkOAlkOH, AlkOAlkOA, AlkOAlkNH2, AlkOAlkNHA, AlkOAlkNAA ', AlkCHOH (CH2) nOH, AlkO (CH2) mHet1 or AlkAr, in which case one of the substituents R2 and R3 - H, R2 and R3 together may also be with an alkylene chain to 6 C atoms, where one or two non-adjacent CH2 groups can be replaced by N and / or O atoms and / or where 1 to 6 H atoms can be replaced by A, OH, OA, (CH2) nHet1, SO2A and / or Hal, Alk means alkylene with 1 to 6 C atoms, where 1 to 4 H atoms can be replaced by F, Cl and / or Br, Cic means cycloalkyl with 3 to 7 C atoms, where 1 to 4 atoms of H can be replaced by A, Hal, OH and / or OA, Het means benzofuranyl which can be mono- or bisubstituted with A, Het 'means a monocyclic heterocycle saturated, unsaturated or aromatic ico with 1 to 4 atoms of N, O and / or S, which can be mono-, bi- or trisubstituted with A, OH, OA, Hal, SO2A and / or> = O (carbonyl oxygen ), Ar means phenyl which is unsubstituted or mono-, bi- or trisubstituted with A, OH, OA, Hal, SO2NH2, SO2NA and / or SO2NAA ', A, A' each mean independently of one another, non-alkyl branched or branched, with 1-10 C atoms, where 1-5 H atoms can be replaced by F, Cl and / or Br, Hal means F, Cl, Br or I, m means 1, 2, 3, 4 , n means 0, 1, 2, 3, 4 as well as its salts, solvates, tautomers and stereoisomers, including their mixtures in all proportions. |
| priorityDate | 2007-10-16-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 637.