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filingDate 2004-12-06-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_5cd975a6e7f064be5c720cd2d7c48d48
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_4bfe8177b4c06a48e7be1dfad291ce02
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publicationDate 2005-07-07-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber WO-2005061439-A1
titleOfInvention Substituted (4-aminocyclohexen-1-yl)phenyl and (4-aminocyclohexen-1-yl)pyridinyl compounds as 5-ht1f agonists
abstract The present invention relates to compounds of formula (I) or a pharmaceutically acceptable acid addition salt thereof, where; X is -C(R4)= or -N=; Ar is phenyl, substituted phenyl, heterocycle, or substituted heterocycle; R1 and R2 are independantly hydrogen or C1-C3 alkyl; R3 is hydrogen, fluoro, or methyl; when X is -C(R4)=, R4 is hydrogen, fluoro, or methyl, provided that no more than one of R3 and R4 may be other than hydrogen; and R5 is hydrogen, methyl, or ethyl. The compounds of the present invention are useful for activating 5-HT1F receptors, inhibiting dural protein extravasation, and for the treatment or prevention of migraine in a mammal.
priorityDate 2003-12-17-04:00^^<http://www.w3.org/2001/XMLSchema#date>
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http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID26136
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419586895
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID83261571
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID226394178
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID21672373
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419489531
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419531062
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID7150
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID226394190
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID458393636
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCP27580
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID21788637

Total number of triples: 627.