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filingDate 2015-03-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_75f7fd267b9d64cf635b5c08b4b0c644
publicationDate 2015-09-11-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber WO-2015132294-A1
titleOfInvention Attenuation of intrapulmonary inflammation
abstract A cyclized compound of the amino acid sequence of formula X 1 -GQRETPEGAEAKPWY-X 2 wherein X 1 comprises an amino acid (sequence) with 1 to 4, in particular 1 to 3 members, comprising natural or unnatural amino acids, in particular selected from the amino acid (sequence) C, KSP, K, ornithin, 4-amino butanoic acid, β-alanine, and X 2 comprises one amino acid, selected from natural amino acids, in particular selected from the group C, D, G and E, and wherein X comprises the N-terminal amino acid at ist first left position and X 2 comprises the C-terminal amino acid at its last right position, optionally in the form of a salt for use in the treatment of inflammation, a pharmaceutical composition for treating inflammation comprising such compound and a method of treating inflammation comprising administering an effective amount of such compound to a mammal in need thereof.
priorityDate 2014-03-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
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