| Predicate |
Object |
| assignee |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_97ddd4d1d0ebc8a7d2c8e7d214d08cf3 |
| classificationIPCInventive |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P31-12
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-70
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07H19-06
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P35-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-7064
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-7052
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-7042
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-7072 |
| filingDate |
1985-03-08-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a36ed92d7844eda9027ec618a1181647
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_237c27731d12a24ccd11fe696526a1f1
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_6300a72a477b9b2ee1c53f63d1fb84ab |
| publicationDate |
1986-09-11-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber |
JP-S61205295-A |
| titleOfInvention |
Anhydrophosphononucleoside and production thereof |
| abstract |
NEW MATERIAL:The compound of formula I (R and R 1 are H or acyl; R 2 and R 3 are H or alkyl). n EXAMPLE: 1'-Deoxy-1' dimethylphosphono-β-D-fructofuranoxyluracil of formula II. n USE: An agent to suppress the biosynthesis of nucleic acid, and expected to be useful as a carcinostatic agent and antiviral agent. n PREPARATION: The anhydronucleoside of formula III is treated with a mineral acid, or acylated after the treatment with a mineral acid. The starting compound of formula III is a novel substance which can be produced from 2, 3'-anhydro-β- D-fructofuranosyluracil of formula IV derived from D-fructose. n COPYRIGHT: (C)1986,JPO&Japio |
| isCitedBy |
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-9501986-A1 |
| priorityDate |
1985-03-08-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type |
http://data.epo.org/linked-data/def/patent/Publication |