http://rdf.ncbi.nlm.nih.gov/pubchem/patent/SK-279315-B6

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filingDate 1989-08-21-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_939e553e62fdcaf6ca4ec9eb2603d676
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c151c497dbd3f27584ebef0a03139b34
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_674007c71b9224ea94c4d1b4d9936a8b
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_00f1c2e6636f33fba4fa8889aa95c457
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_2291b44d23deaa73199d0ac3636402d5
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a717192b4edcb7b4a122b0e3677c8b02
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_5ef1a673e394aae29aa2f9e506455b25
publicationDate 1998-09-09-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber SK-279315-B6
titleOfInvention PEPTIDES ANTAGONING EFFECTS OF BRADYCININ AND METHOD
abstract Peptides of the formula (I) in which A is hydrogen, alkyl, alkanoyl, alkoxycarbonyl, alkylsulphonyl, cycloalkyl, aryl, arylsulphonyl, heteroaryl or the residual of an amino acid, each of which can optionally be substituted; B is the residual of a basic amino acid; C is the residual of a di- or tripeptide; E is the residual of an aromatic amino acid; F is, independently of one another, an amino acid which is optionally substituted in the side chain or is a direct bond; G is the residual of an amino acid; F' is defined as F and it can be -NH-(CH2)2-8 or optionally a direct bond; I is -OH, -NH2 or -NHC2H5; K is a radical -NH(CH2)1-4 -CO- or is a direct bond, have bradykinin-antagonistic action. Their therapeutic uses comprise all pathological states which are promoted, induced or sustained by bradykinin and bradykinin-related peptides. The peptides of the formula I are prepared by known methods of peptide synthesis.
priorityDate 1988-11-24-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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