http://rdf.ncbi.nlm.nih.gov/pubchem/patent/MX-2007013154-A

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filingDate 2006-04-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_014a8207fefe7e5ad35e35f84af3bfbf
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c9545bda40f0e1d9d8722b5615996fe3
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a63945700a7f2dcc919323831200579e
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_10210d022b783496641a925e80b3a2f3
publicationDate 2008-01-21-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber MX-2007013154-A
titleOfInvention FUSIONED HETEROCICLIC COMPOUNDS.
abstract An antagonist is provided to the CRF receptor comprising a compound of the formula (I): (see formula (I)) wherein R1 is an optionally substituted hydrocarbyl, an optionally substituted C-linked heterocyclic group, an optionally N-linked heteroaryl group substituted, a cyano or an acyl; R2 is an optionally substituted cyclic hydrocarbyl or an optionally substituted heterocyclic group; X is oxygen, sulfur or -NR3- (where R3 is a hydrogen, an optionally substituted hydrocarbyl or an acyl); Y1, Y2 and Y3 are each an optionally substituted carbon or a nitrogen, with the proviso that one or less of Y1, Y2 and Y3 is nitrogen; and Z is a bond, -CO-, oxygen, sulfur, -SO-, -SO2-, -NR4-, -NR4-alq-, -CONR4- or -NR4CO- (where alq is a C1-4 alkylene optionally substituted and R4 is a hydrogen, an optionally substituted hydrocarbyl or an acyl); or a salt thereof or a prodrug thereof.
priorityDate 2005-04-27-04:00^^<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: 527.