http://rdf.ncbi.nlm.nih.gov/pubchem/patent/AR-070020-A1

Outgoing Links

Predicate Object
assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_966a6c1f382ec9bcb5e3839dfd73e5b8
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P1-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P1-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K31-4439
filingDate 2008-08-19-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_427556bd36ddf3c314f8888eebb7ef81
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_4f7920b13c87bcdc8242fc19bdf4358b
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_6621beaadf0b75434175432188d2c17a
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publicationDate 2010-03-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber AR-070020-A1
titleOfInvention USE OF MGLUR5 ANTAGONISTS FOR THE TREATMENT OF GERD, PHARMACEUTICAL COMPOSITION AND TREATMENT METHOD
abstract Claim 1: Use of a compound of the general formula (1) wherein one of A or E is N and the other is C; R1 is halogen; R2 is C1-6 alkyl; R3 is phenyl, pyridinyl, pyrazinyl, pyrimidinyl or pyridazinyl, which are optionally substituted by one, two or three substituents chosen from the group consisting of halogen, C1-6 alkyl, C1-6 alkoxy, C1-6 haloalkyl or C2-6 haloalkoxy ; R4 is CHF2, CF3, CH2OH or C1-6 alkyl; In the form of free base or acid addition salt they are very effective for the treatment, prevention and / or delay of the progress of gastro-esophageal reflux disorder (GERD). Claim 13: Pharmaceutical composition according to claim 12 further containing an anti-secreting agent, preferably chosen from the group consisting of proton pump inhibitors (PPI) and histamine H2 receptor antagonists.
priorityDate 2007-08-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

Incoming Links

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Total number of triples: 19.