http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-2007078167-A1

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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-444
filingDate 2006-09-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_48fc8f1ef9a3fd6bf933958bed776b52
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c1c0e3022a12a6494cb18ed5b5436a4e
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e806a8a072680037be276158c38d8581
publicationDate 2007-04-05-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-2007078167-A1
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-γ 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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