http://rdf.ncbi.nlm.nih.gov/pubchem/patent/ES-2347182-T3
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_a8f70c5b59b293a0220e30a752bb017f |
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K31-5025 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P21-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P21-02 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P25-20 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P25-22 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P25-08 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P25-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P23-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D487-04 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P43-00 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P25-08 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P25-22 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P25-20 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D487-04 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-5025 |
| filingDate | 2007-03-28-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| grantDate | 2010-10-26-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_98b55cd43db2bd969adbbf14fc8c5094 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_9d08f1812f4d495661d732722d284830 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ea0828d6851c41354f214314061b4106 |
| publicationDate | 2010-10-26-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | ES-2347182-T3 |
| titleOfInvention | IMIDAZO (1,2-B) PIRIDAZINAS, PROCEDURES FOR ITS PREPARATION AND ITS USE AS GIGA RECEIVER LINKS. |
| abstract | Imidazo [1,2-b] pyridazine compound of formula (I) ** (See formula) ** where R1 and R2 are independently selected from the group consisting of hydrogen, linear or branched (C1-C6) alkyl, alkenyl (C2) -C6), (C2-C6) alkynyl, (C3-C6) cycloalkyl, (C2-C6) haloalkyl, hydroxy, -O-(C1-C6) alkyl, phenoxy, -S-(C1-C6) alkyl, phenylthio , halogen, nitro, cyano, amino, (C1-C6) alkylamino, dialkylamino (C1-C6), pyrrolidinyl, morpholinyl, piperidinyl, N-(C1-C6) piperazinyl, phenyl optionally substituted with 1 to 5 Z groups and heteroaryl optionally substituted by 1 to 5 Z groups; R3 and R4 are independently selected from the group consisting of hydrogen, linear or branched (C1-C6) alkyl, (C2-C6) alkenyl, (C2-C6) alkynyl, (C3-C6) cycloalkyl, (C1-C6) hydroxyalkyl , amino, -NH-(C1-C6) alkyl, -N-dialkyl (C1-C6), pyrrolidinyl, morpholinyl, piperidinyl, -N-(C1-C6) piperazinyl, -N-acyl (C1-C6) piperazinyl , phenyl optionally substituted by 1 to 5 Z groups and heteroaryl optionally substituted by 1 to 5 Z groups, or both R3 and R4 can form, together with the nitrogen atom to which they are attached, an optionally substituted 5-6 membered heterocyclic ring by 1 to 5 Z groups, with the proviso that R3 and R4 are not simultaneously hydrogen; X is selected from CO and SO2; Z is selected from the group consisting of linear or branched (C1-C6) alkyl, (C2-C6) alkenyl, (C2-C6) alkynyl, (C3-C6) cycloalkyl, (C2-C6) haloalkyl, hydroxy, -O -C1-C6 alkyl, phenoxy, -S-C1-C6 alkyl, phenylthio, halogen, nitro, cyano, amino, C1-C6 alkylamino and C1-C6 dialkylamino; and pharmaceutically acceptable salts, polymorphs, hydrates, tautomers, solvates and stereoisomers thereof. |
| priorityDate | 2006-03-29-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
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