http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-2002161221-A1

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filingDate 2001-08-09-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_7da88e65407b622e067cda9e5e9f7437
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_1507032c360dbe28f8f8395e8b7a2edd
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_62345a69e6293df7a9b0e8afc58042c7
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_d244c1bfc6ea0af15589ff8ee61e12dd
publicationDate 2002-10-31-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-2002161221-A1
titleOfInvention Ether type lipid a 1-carboxylic acid analogs
abstract A compound of formula (I) below, which exhibits excellent macrophage activity inhibitory action, is useful for the treatment or prophylaxis of inflammatory disorders, autoimmune diseases or septicemia. In a preferred embodiment, R 1 and R 3 each represents a C 1 -C 20 alkanoyl group which may optionally be substituted with one or more substituent groups selected from substituent group A, R 2 and R 4 each represents a C 1 -C 20 alkyl group which may optionally be substituted with one or more substituent groups selected from substituent group A, R 5 is a hydrogen atom, a halogen atom, a hydroxy group, or a C 1 -C 6 alkoxy group, and substituent group A is a halogen atom, a hydroxy group, an oxo group, a C 1 -C 20 alkoxy group, or a C 1 -C 20 alkanoyloxy group.
priorityDate 1999-02-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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Total number of triples: 1364.