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filingDate 2004-12-17-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2010-09-07-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_9fc198da5dd5d73b5428a801d98d7357
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_8cbc1421121025fa4dc775064620fb2f
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publicationDate 2010-09-07-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-7790754-B2
titleOfInvention Alpha-hydroxy amides as bradykinin antagonists or inverse agonists
abstract α-Hydroxy amide derivatives of the general formula (I) are bradykinin B1 antagonists or inverse agonists useful in the treatment or prevention of symptoms such as pain and inflammation associated with the bradykinin B1 pathway. R 2a is selected from (1) a group selected from R a . (2) (CH 2 ) n NR b C(O)R a . (3) (CH 2 ) n NR b SO 2 R d . (4) (CH 2 ) n NR b CO 2 R a . (5) (CH 2 ) k -heterocycle optionally substituted with 1 to 3 groups independently selected from halogen.nitro, cyano.OR a .SR a .C 1-4 alkyl and C 1-3 haloakyl wherein said heterocycle is (a) a 5-membered heteroaromatic ring having a ring heteroatom selected from N.O and S. and optionally having up to 3 additional ring nitrogen atoms wherein said ring is optionally benzo-fused; or (b) a 6-membered heteromatic ring containing from 1 to 3 ring nitrogen atoms and N-oxydes thereof. Wherein said ring is optionally benzo-fused. (6) (CH 2 ) k CO 2 R a . and (7) (CH 2 )C(O)NR b R c . R 2b is OH or a group selected from R 2a ; or R 2a and R 2b together with the carbon atom to which they are attached form a 3- to 7-membered carbocyclic ring optionally substituted with 1 to 4 groups independently selected from halogen. OR a . C 1-4 alkyl and C 1-4 haloalkyl.
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priorityDate 2003-12-22-04:00^^<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: 1731.