http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2004143046-A

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_7f6e33603375c486b0ab3505830af9e8
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-7048
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07H15-26
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P31-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P29-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P37-06
filingDate 2002-10-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_995aaabb55bb5861c659df3d14dc57d0
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_bb79a821a67cc99719e47d54d5647ca7
publicationDate 2004-05-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-2004143046-A
titleOfInvention Pharmaceutical containing lipid A1 carboxylic acid analog
abstract An object of the present invention is to provide a compound having an excellent macrophage activity inhibitory activity and useful as an anti-inflammatory agent, an anti-autoimmune disease agent, an immunosuppressant or an anti-sepsis agent. The general formula (I) Embedded image [In the formula, one of R 1 and R 3 is a C9-15 alkyl group, the other is a hydrogen atom or a C1-6 alkyl group, and the other one of R 2 and R 4 is a C10-16 alkenyloxy-substituted C9-alkyl group. 15 alkyl group, the other is, C10-16 alkyl group, R 5 represents a hydroxyl group, C1-6 alkoxy group, a halogen atom. ] Or a pharmacologically acceptable ester thereof or a pharmacologically acceptable salt thereof as an active ingredient. [Selection diagram] None.
priorityDate 2002-10-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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