http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-5925672-A

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P25-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K31-366
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P29-00
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-366
filingDate 1996-12-06-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1999-07-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_af9b039a243ed9ef888d820ba090ae7d
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_d0fe16106059f5b160734a7d548f31a5
publicationDate 1999-07-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-5925672-A
titleOfInvention Methods of treating mental diseases, inflammation and pain
abstract Methods are disclosed for treating or preventing disorders such as mental diseases, inflammation and pain by inhibiting the enzyme anandamide amidohydrolase. A therapeutically effective level of an anandamide amidohydrolase inhibitor is administered such as a therapeutically effective level of a haloenol lactone. Preferably, the haloenol lactone is of the formula: ##STR1## wherein R is hydrogen, R 1 is a halogen, and R 2 is selected from the group consisting of aryl, aryloxy, and heteroaryl radicals, derivatives of said haloenol lactones, and mixtures thereof. The haloenol lactone, E-6-(bromomethylene)tetrahydro-3-(1-naphthalenyl)-2H-pyrane-2-one, is most preferred.
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