http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-2382212-A1

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filingDate 2010-01-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ebc1266abfb60b6fc8028cce9c61cc07
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ae6210b9a52e41dcb3f7585fbb02012d
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_879e0c34fb2b9f7552343d79b3ea0286
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_5bc3f1deae0c83258c93ca7208a24bf5
publicationDate 2011-11-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-2382212-A1
titleOfInvention Substituted oxadiazole derivatives as s1p agonists in the treatment of autoimmune and inflammatory diseases
abstract Disclosed are compounds of Formula (I) [INSERT CHEMICAL STRUCTURE HERE] (I) or pharmaceutically acceptable salts thereof, wherein Q is [INSERT CHEMICAL STRUCTURE HERE] or [INSERT CHEMICAL STRUCTURE HERE]; R1 is alkyl or aryl, said aryl optionally substituted with one to five substituents independently selected from C1 to C6 alkyl, C1 to C4 haloalkyl, OR4, and/or halogen; and R2, R3, R4, and n are defined herein. Also disclosed are methods of using such compounds as selective agonists for G protein-coupled receptor S1P1, and pharmaceutical compositions comprising such compounds. These compounds are useful in treating, preventing, or slowing the progression of diseases or disorders in a variety of therapeutic areas, such as autoimmune diseases and vascular disease.
priorityDate 2009-01-23-04:00^^<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: 909.