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filingDate 2017-04-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_dd6e6b823155b435ce40b171fd4b2d90
publicationDate 2018-11-13-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-108785317-A
titleOfInvention Use of Cinnamon Cortex C21 Steroids in the Preparation of IDO Inhibitors
abstract The invention belongs to the field of medicines or health care products, and in particular relates to the application of C21 steroids of Cyperus saponica in the preparation of IDO inhibitors. The present invention finds through research that the inhibitory activity of bariclin A, baricacidin F, baricacidin U and baricacidin T on intracellular IDO is better than that of the positive control drug 1-methyl tryptophan (1-MT ) has significant IDO inhibitory activity, and can be used to treat cancer, Alzheimer's disease, autoimmune diseases, ankylosing spondylitis, bacterial infections, cataracts, mood disorders, and depression or anxiety disorders.
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