http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-0372940-A3
Outgoing Links
| Predicate | Object |
|---|---|
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07F9-65515 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P29-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D307-58 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07F7-0814 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D307-58 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P29-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07F9-655 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07F7-08 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-365 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D307-33 |
| filingDate | 1989-12-07-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationDate | 1991-03-06-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | EP-0372940-A3 |
| titleOfInvention | Anti-inflammatory 2-furanones |
| abstract | The present invention provides compounds nof the formula (I): n nin which: nA is C₈-C₂₀alkyl or CH(R₁)R; nR is C₇-C₂₀alkyl; nR₁ is hydroxy, OCOR₂, n2-(methoxy)ethoxymethoxy, halogen and NHR₃; nR₃ is H, C₁-C₆ alkanoyl, COCF₃ and nC₁-C₆ sulfonyl; nR₂ is C₁-C₁₄alkyl or amino optionally nN-substituted by one α-(C₁-C₄alkyl)benzyl group, by none or two C₁-C₄alkyl groups or by one phenyl group; nor OP(R₄R₅); or nR is 2-(methoxy)ethoxymethoxymethyl and R₁ is nOCO-(C₇-C₁₄alkyl); or nR is CH(OCOC₁-C₄alkyl)C₇-C₂₀alkyl and nR₁ is OCO(C₁-C₄alkyl); and nR₄ = R₅ is H or C₁-C₄ alkyl, n n npharmaceutical compositions containing them, a process nfor their preparation and their use in the treatment nof inflammation or an allergic response in a mammal, nor psoriasis. |
| priorityDate | 1988-12-07-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 25.