http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-S6284098-A
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_97ddd4d1d0ebc8a7d2c8e7d214d08cf3 |
| classificationCPCAdditional | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/Y02P20-55 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07K5-08 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P31-10 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07F7-18 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07K5-06 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07K7-06 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D309-12 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K38-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07K5-10 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D207-16 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P31-04 |
| filingDate | 1985-10-09-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_250de8d032b2ab9ed58b55361786ee17 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c35413ecabcc205ef3a6d26169107d96 |
| publicationDate | 1987-04-17-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | JP-S6284098-A |
| titleOfInvention | Synthetic intermediate for echinocandin and production thereof |
| abstract | NEW MATERIAL:A compound expressed by formula I [R 1 is H or tert- butylidemethyl; R 2 is H or tetrahydropyranyl; R 3 is H or tert-butyldimethylsilyl; A is hydroxyl group, pyridinethiol, etc.; B is H or formula II (D is H, benzyloxycarbonyl, etc.)] n EXAMPLE: ( 2S, 4R-N-Linoleyl-2-amino-4-O-Ct-butyldimethylsilyl )-5, 5-dimethoxy pentanolyl-O-tert-butyldimethylsilyl-threonyl-[( 4R )-4-hydroxy]prolyl-[( 3R )- hydroxy]homotyrosyl-threonly-[( 3S, 4S )-3-hydroxy-4-methyl]prolinamide. n USE: An antifungal and antiyeast agent. n PREPARATION: For example, a threonine derivative expressed by formula III is activated in an organic solvent and then reacted with a homotyrosine deriva tive expressed by formula IV and the protecting group is removed to afford the aimed compound expressed by formula I. n COPYRIGHT: (C)1987,JPO&Japio |
| priorityDate | 1985-10-09-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 32.