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filingDate 1992-03-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_741b1f040e98a2443632d025465b98c3
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publicationDate 1993-09-07-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-H05229958-A
titleOfInvention Osteoporosis treatment
abstract (57) [Summary] (Modified) [Structure] General formula H-X ↑ 1-Cys-ABBABA-Ser-X ↑ 2-Y (In the formula, A is an amino acid residue Val. , Leu, Ile, Nle, B Is the amino acid residues Arg, Lys, Gln, His, Ser, X ↑ 1 And X ↑ 2 is a single bond or Gly, Ala, Val, Arg, Asn, Ser, Phe, Pro, Leu, Glu, Asp, Lys, Th A peptide fragment consisting of 1 to 10 amino acid residues selected from r, His, Tyr, Nle, and Ile, Y is a hydroxyl group or an amino group), and has a human interleukin-1 binding ability or a salt thereof. A therapeutic agent for osteoporosis containing as an active ingredient. [Effect] It is useful for treatment of osteoporosis associated with IL-1, such as para-articular osteoporosis associated with rheumatoid arthritis, alveolar bone resorption associated with periodontitis, postmenopausal high-rotation osteoporosis, and senile osteoporosis.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-02066063-A1
priorityDate 1991-12-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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