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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07K14-585
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K38-23
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07K14-575
filingDate 1987-02-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_cfe30541b329153cf02fa1a3c5bc50a6
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e254595808f1a3f5f16fda0dce89b240
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publicationDate 1988-08-23-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-S63203699-A
titleOfInvention Novel calcitonin derivative
abstract NEW MATERIAL:A compound (salt) expressed by the formula [X is alanine or threonine; R is (substituted)benzyl]. n USE: A remedy for hypercalcemia, osteoporosis and bone Behcet's diseases. n PREPARATION: For example, BHA resin is placed in a reaction vessel for peptide solid-phase synthesis, reacted with a solution of an amino group-protected proline which is a C-terminal amino acid in dichloromethane in the presence of a condensing agent and linked to the resin. The amino-protecting group is then removed. Amino acids having protected amino groups are subsequently reacted according the amino acid sequence of the peptide and amino-protecting groups are removed. The above-mentioned operation is repeated to successively link the amino acids to afford a resin peptide, which is then treated with hydrogen fluoride to carry out elimination of the peptide from the resin and removal of all the protecting groups. Thereby the compound expressed by the formula is obtained. n COPYRIGHT: (C)1988,JPO&Japio
priorityDate 1987-02-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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Total number of triples: 28.