http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-2018282367-A1

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_2caaba601fd6460c7b37706d920d42e2
classificationCPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K38-00
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07K7-16
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07K7-16
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filingDate 2016-10-06-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b19757da04d086d00a3ab3383a3a665b
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_8f5568b37422a1ddece8bc4249e0f5dd
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b9a85539b70cdf3e26c28ad83a5cac3c
publicationDate 2018-10-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-2018282367-A1
titleOfInvention New methods for making barusiban and its intermediates
abstract The present invention relates to new solid phase peptide methods for synthesizing analogues that exhibit oxytocin antagonist activity, specifically Barusiban and its intermediates. Specifically, the present invention relates to a solid phase process for preparing a compound having the formula c[AA 1 -AA 6 ]-AA 7 -ol, wherein AA 1 is propionic acid, AA 2 is preferably D-Trp, AA 3 is Ile, AA 4 is preferably AlloIle, AA 5 is Asn, AA 6 is hCy, and AA 7 is preferably N-Me-Orn-ol, or a pharmaceutically acceptable salt or solvate thereof.
priorityDate 2015-10-06-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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