http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-S6191197-A

Outgoing Links

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_5929f2d6f4dba84be8dd3a8ba633db12
classificationCPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/Y02P20-55
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12N15-00
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12N15-09
filingDate 1984-10-09-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_07de6eb4eec4e1e2d6a943202cd1c890
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_85e99fe704b04a9774ff656b3259c950
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e84994e5f68dd2c96af251fdd3fdd69b
publicationDate 1986-05-09-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-S6191197-A
titleOfInvention Polypeptide
abstract NEW MATERIAL:A compound of the formula (R 1 , R 2 , R 3 are H, protecting groups). n USE: A reagent for elucidating the mechanism of resistance manifestation in a bacterium resisting antibiotics or a reagent for studying biotechnology and molecular biology. n PREPARATION: For example, the benzyl ester of glycine which is the C-terminal aminoacid of this peptide is dissolved in DMF together with alanine whose amino group is protected with t-butoxycarbonyl group, p-toluenesulfonate salt and triethylamine. Then, a condensation reagent such as N,N'-dicyclohexyl- carbodiimide is added thereto under cooling to effect reaction. The amino- protecting groups are removed, then the operations are repeated in accordance with the aminoacid sequence of the peptide, further the protecting groups are eliminated as needed to give the compound of the formula. n COPYRIGHT: (C)1986,JPO&Japio
priorityDate 1984-10-09-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

Incoming Links

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Total number of triples: 35.