http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-S6251618-A
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_52a65b677bbedbe7bf090dd556a7cc43 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-7024 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07H13-12 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-70 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N47-20 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P31-12 |
| filingDate | 1985-08-30-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_690d958623c8e155aa3a352ef9896a5a |
| publicationDate | 1987-03-06-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | JP-S6251618-A |
| titleOfInvention | Virus inactivator |
| abstract | PURPOSE: A virus inactivator, containing a novel O-arylcarbamoylaldose as an active constituent, having oxgen radical forming ability and virus inactivating ability and capable of exhibiting nucleic acid cleaving action in vitro. n CONSTITUTION: A virus inactivator obtained by using preferably an O- aralcarbamoylaldose having pentasaccharide and hexasaccharide in the aldose part as an active constituent. The O-arylcarbamoylaldose has nucleic acid cleaving action and is capable of inactivating viruses, e.g. tobacco mosaic virus or bacteriophage ϕ×174, in vitro. The O-arylcarbamoylaldose can be obtained by reacting aldose with an aryl isocyanate in a solvent. Specific examples thereof include compounds expressed by formulas I, II, etc. n COPYRIGHT: (C)1987,JPO&Japio |
| isCitedBy | http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2005092907-A3 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2006111783-A1 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-7790689-B2 |
| priorityDate | 1985-08-30-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 23.