http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-S54151919-A
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_6831b19bfc354357342f7c7da79fc162 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-7024 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P35-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07H13-12 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-70 |
| filingDate | 1978-05-16-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c7516e45e46ec6d1a9a76aa982362027 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_85ed5e4a7668a6a19770deac23ba64be http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_dd7eec6b55be0ba2b1000d535090fb63 |
| publicationDate | 1979-11-29-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | JP-S54151919-A |
| titleOfInvention | Preparation of derivative of nitrosourea |
| abstract | NEW MATERIAL:A derivative of nitrosourea of formula I (R 1 =straight chain alkyl of C 1W20 ; R 2 is a monosaccharide having hemiacetal OH at the 1 position or a disaccharide residue without the hydroxyl group at the 1 position). n EXAMPLE: 1-(2-Chloroethyl)-1-nitroso-3-methyl-3-D-glucopyranosylurea. n USE: Non-toxic antileukemic agents, antineoplasmic agents, etc. n PROCESS: A compound of formula I is obtained by the reaction of a urea derivative of formula II and nitrogen tetraoxide. The derivative is dissolved in a proper solvent and nitrogen tetraoxide is introduced therein, to carry out the reaction. Or nitrogen tetraoxide is dissolved in a proper solvent and the solution obtaind is mixed to the derivative. n COPYRIGHT: (C)1979,JPO&Japio |
| priorityDate | 1978-05-16-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 25.