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filingDate 1995-06-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 1998-03-03-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-H10502349-A
titleOfInvention Method for inhibiting the binding of integrin α 4 and β 1 to VCAM-1 or fibronectin
abstract (57) Abstract The present invention relates to an isolated and purified cyclic peptide of 5 to about 13 residues, modeled on a part of the CS1 peptide. The peptide of the present invention preferably has the amino acid residue sequence of SEQ ID NOs: 2 to 14 or 16 to 42. The present invention further, alpha 4 beta 1 integrin, VCAM-1, relates to a method of selectively inhibiting the binding of proteins, such as fibronectin or invasin, the method, the presence of an inhibitory effective amount of the peptide, alpha 4 cells expressing beta 1 integrin including exposure to the protein. The invention further relates to a pharmaceutical composition comprising a physiologically acceptable carrier and a cyclic peptide of the invention.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2001089499-A
priorityDate 1994-06-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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