http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-1942889-A2

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filingDate 2006-09-08-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_9249d62106130f29d47d979aa49a9a73
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_cb725e79860ae1ce9f939f57058ae485
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_d4659447651e0e6982f59af87eed0fd8
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f7bcd26a69e3f817f777ff9dd1316f25
publicationDate 2008-07-16-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-1942889-A2
titleOfInvention Use of bipyridine compound 'caerulomycin a' derivatives and analogs thereof as immunosuppressive agents
abstract The present invention relates to an isolated bioactive molecule Caerulomycin A, derivatives and analogs thereof as effective immunosuppressive agents. The immunosuppressive property of the compound is targeted in particular against the lymphocytes, CD4+ T cells, CD8+ T cells and B cells and in the production of IL-4 and IFN-Ϝ and antibodies. The compound operates through a mechanism by downregulating the expression of activation marker CD28 and upregulating the immunosuppressive marker CTLA-4. Caerulomycin A has previously been isolated from Streptomyces caeruleus and found to have useful antifungal activity. Prior to the present invention however, this compound had not been determined to have immunomodulatory activity.
priorityDate 2005-09-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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