http://rdf.ncbi.nlm.nih.gov/pubchem/patent/MX-2009006582-A

Outgoing Links

Predicate Object
assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_cf0a9220978baa4415ff07a3c609b022
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P9-14
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P13-10
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P25-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C335-12
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P29-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K31-17
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P11-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C275-24
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P43-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P1-00
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P29-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C275-24
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-17
filingDate 2007-12-06-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_76a753c5497ab43077071356cb0bd6ff
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_428e53f9d74b9554dbdef07df2895500
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a92322e6ca5c05091b458cfb2ee60f41
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_d694a9b49e3c237209802ced3f76dd82
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ed4ccb190239a9ed3b8e8412adbdd41d
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_6524e748fad5a666d5f202d9f6aab463
publicationDate 2009-07-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber MX-2009006582-A
titleOfInvention DERIVATIVES OF DIBENCIL UREA O-SUBSTITUTED AS ANTAGONISTS OF THE VANILOID RECEIVER OF THE RECEIVING CHANNEL OF THE TRANSITORY POTENTIAL 1.
abstract The invention relates to compounds of formula (I) (see formula I) wherein R is selected from halogen, alkyl, alkoxy, aryl and heteroaryl; R1 is selected from 2-hydroxyethyl, 2,3-dihydroxypropyl, 3-hydroxypropyl, 2,2-dihydroxyethyl, 3,3-dihydroxypropyl, 1,3-dioxolane-ethyl, 1,3-dioxane-methyl, 1,3- dioxolane-methyl, 1,3-dioxane-ethyl, 3-fluoro-2-hydroxypropyl, 3-carboxy-2-hydroxy-propyl, 3-chloro-2-hydroxypropyl, 2-hydroxypropyl, 2-hydroxy-propen-2- yl, morpholinoethyl, piperazinoethyl, hydroxymethyl, benzyl, 4- (hydroxymethyl) benzyl, 4-chlorobenzyl, 4-fluorobenzyl and 4-hydroxybenzyl; R2 is tert-butyl or trifluoromethyl; R3 is independently selected from hydrogen, carboxy, cyano, alkyl or hydroxyalkyl; The compounds of formula (I) can be used for the preparation of pharmaceutical compositions for the therapy of inflammatory conditions, such as chronic neuropathic pain, over-active bladder syndrome, tumor pain, hemorrhoids, inflammatory hyperalgesia, post-intervention pain, extraction dental, respiratory and gastrointestinal diseases.
priorityDate 2006-12-21-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

Incoming Links

Predicate Subject
isDiscussedBy http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID458394834
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID458394736
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID458393374
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID458393353
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID458393640
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID457311044
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419890815
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID458394739
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID1031
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID458393349
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID458397482

Total number of triples: 38.