http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-RE28034-E
Outgoing Links
| Predicate | Object |
|---|---|
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D217-04 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D217-04 |
| filingDate | 1972-12-14-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| grantDate | 1974-06-04-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationDate | 1974-06-04-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | US-RE28034-E |
| titleOfInvention | Alkylsulfinylalkyl- and sulfonyl-nalkyl-i,z,j,x.tetrahydroisoqijinolines |
| abstract | N-SUBSTITUTED 1,2,3,4-TETRAHYDROISOQUINOLINES EXEMPLIFIED BY 2-(3-ETHYLSULFINYLPROPYL)- 1,2,3,4-TETRAHYDROISOQUINOLINE. 2-(CH3-CH2-SO-(CH2)3-)-1,2,3,4-TETRAHYDROISOQUINOLINE EXERT CARDIOVASCULAR EFFECTS WHEN ADMINISTERED AS THEIR HYDROCHLORIDES. SUCH SULFINYL COMPOUNDS ARE PREPARED BY OXIDATION OF THE CORRESPONDING THIO ETHERS, WHICH MAY ALSO BE OXIDIZED TO THE CORRESPONDING SULFONYL COMPOUNDS. SUBSTITUTION ON THE AROMATIC AND HETEROCYCLIC RINGS AND VARIATIONS IN THE CHAIN ARE DISCLOSED. |
| isCitedBy | http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-5817614-A http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-8803137-A1 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-5710116-A http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-4975438-A http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-0266949-A1 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-5576282-A |
| priorityDate | 1972-12-14-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 90.