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filingDate 2008-11-13-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_233b175a1d6c8c31520778b28b17e803
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publicationDate 2009-05-21-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-2009106290-A
titleOfInvention Novel anti-angiogenic peptide, polynucleotide encoding it, and method for inhibiting angiogenesis
abstract Compounds useful in the treatment of angiogenic diseases in mammals, particularly safe for therapeutic use and exhibiting little or no toxicity to, for example, normal (ie, non-cancerous) cells The present invention provides a compound serving as an anti-angiogenesis inhibitor, which exhibits selective toxicity against pathological symptoms by selectively inhibiting the proliferation of endothelial cells. Structural formula A-B-C-X-Y wherein A is absent or a nitrogen protecting group, Y is absent or a carboxylic acid protecting group, and B is a natural amino acid residue. , C is R 1 —R 2 —R 3 —R 4 [Lysyl, Leucyl or Arginyl, Tyrosyl, etc., Aspartyl], X is Absent or Natural Amino Acid Residue, etc.] Fragment of Mammalian Kringle (5) And Kringle (5) a method and compound for inhibiting angiogenic diseases, wherein the fusion protein is a compound for treating angiogenic diseases. [Selection figure] None
priorityDate 1996-05-03-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCC5D9N8
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http://rdf.ncbi.nlm.nih.gov/pubchem/gene/GID615026
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http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCP21329
http://rdf.ncbi.nlm.nih.gov/pubchem/gene/GID44999375
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http://rdf.ncbi.nlm.nih.gov/pubchem/gene/GID1991
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http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCQ8ZV53
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http://rdf.ncbi.nlm.nih.gov/pubchem/gene/GID54250
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http://rdf.ncbi.nlm.nih.gov/pubchem/gene/GID1487533
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Total number of triples: 778.