http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-8252751-B2

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_6c900f6a43c3b25f06ddfaffa37538ca
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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07H15-26
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P3-04
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07H15-24
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P3-10
filingDate 2008-11-25-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2012-08-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_1d98cc55f18f4a4b01f2ce09274b9fec
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_34a0bab45d6345b4ae4c9c51aba5742e
publicationDate 2012-08-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-8252751-B2
titleOfInvention Organic compounds
abstract The present invention relates to a compound The instant invention relates to a compound of formulae (I A), (I B), (X A), (X B), (Y A) or (Y B), wherein R′ represents and R″ represents hydrogen, hydroxy, C1-C7alkoxy, C1-C8-alkanoyloxy, or R5R4N—CO—O—, where R4 and R5 independently are C1-C7alkyl or phenyl which is unsubstituted or substituted by a substitutent selected from C1-C7alkyl, C1-C7alkoxy, halogen and trifluoromethyl and where R4 additionally is hydrogen; or R4 and R5 together represent C3-C6alkylene; in free form or in form of a pharmaceutically acceptable acid addition salt. Compounds of formulae (I A), (I B), (X A), (X B), (Y A) or (Y B) inhibit DPP-IV (dipeptidyl-peptidase-IV) activity. They are therefore indicated for use as pharmaceuticals in inhibiting DPP-IV and in the treatment of conditions mediated by DPP-IV, such as non-insulin-dependent diabetes mellitus, arthritis, obesity, osteoporosis and further conditions of impaired glucose tolerance.
priorityDate 2007-11-30-04:00^^<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: 891.