| Predicate |
Object |
| assignee |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_7f6e33603375c486b0ab3505830af9e8 |
| classificationCPCAdditional |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/Y02P20-55 |
| classificationIPCInventive |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-7024
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07H13-06
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07H11-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P35-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-70
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P37-04 |
| filingDate |
1991-06-19-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c6ba83d7366e3a86df84e9a52d228ba8
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e20bf3aefc3b5f5f7e36727913facec7
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c16dcd795fe93e02a181b0c81cbb9844
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f0bfcaf7bef97294eb0f2d557261177d
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_995aaabb55bb5861c659df3d14dc57d0
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_aa6fbb7c1693c40d88561dace2b34d6f
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_6fc0529b84aea935efebe9aa78d99606 |
| publicationDate |
1992-08-24-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber |
JP-H04235193-A |
| titleOfInvention |
Lipid x relative substance |
| abstract |
PURPOSE: To obtain a new lipoid X relative substance having antitumor action based on macrophage activation and low toxicity. n CONSTITUTION: A compound shown by formula I [one of R 1 and R 4 is H and the other is P(O)(OH) 2 ; R 2 and R 3 are 6-20C aliphatic acyl which may be replaced with a group selected from substituent group of group A; R 5 is H or OH-protecting group; R 2 and R 3 are not simultaneously unsubstituted 6-20C acyl, 6-20C acyl replaced with OH and 6-20C aliphatic acyl replaced with 6-20C aliphatic acyloxy; substituent group of group A is halogen, OH, 6-20C aliphatic acyloxy or 6-20C aliphatic acyloxy replaced with halogen] and a salt thereof such as 2-deoxy-2-[(3'R)-3-hydroxymyristoylamino]-3-0-[(2"RS,3"SR)-2"-fluoro-3"- hydroxymyristoyl]-α-D-glucopyranosyl-1-phosphate. A compound shown by the formula I having phosphate residue bonded to the 1-position is obtained from glucosamine hydrochloride shown by formula II as a starting substance. n COPYRIGHT: (C)1992,JPO&Japio |
| isCitedBy |
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-4496369-B2
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-7737129-B2
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2007039359-A
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-7994154-B2 |
| priorityDate |
1990-06-22-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type |
http://data.epo.org/linked-data/def/patent/Publication |