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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K31-282
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K38-08
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-337
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-282
filingDate 2006-06-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_538b9590a6038a13458eff698fc81b6a
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b5087f08670f065c007a9df60ccebd1b
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_8651cdada7912db40027ac6f9ddac651
publicationDate 2007-01-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-2007015715-A1
titleOfInvention Method of treating cancer and neuropathic complications induced by chemotherapeutic agents using selective Bradykinin B1 receptor antagonists
abstract The present invention relates to a method for the use of a bradykinin B1 receptor antagonist of formula I: n nX—CO-Aaa 0 -Aaa 1 -Aaa 2 -Aaa 3 -Gly-α(Me)Phe-Ser-D-βNal-Aaa 8 -OH  (I)nor a pharmaceutically acceptable salt or hydrate thereof wherein: n X is C n H 2n+1 or C i H 2i —C 6 H 5 , where n is an integer from 1 to 3, and i is an integer from 0 to 3; Aaa 0 is Lys, Orn or Cit; Aaa 1 is Arg or Cit, and preferably Arg; Aaa 2 is Oic, Hyp or Pro, and preferably Oic; Aaa 3 is Pro or Oic, and preferably Pro; and Aaa 8 is Ile, Leu, Nle, and preferably Ile, for the treatment of metastases, cancers and/or chemotherapy-induced neuropathies, comprising the administration of said compound to a patient in need of such treatment. The present invention also relates to compositions containing such antagonists and the uses thereof.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2018524401-A
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-7091241-B2
priorityDate 2004-08-19-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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