http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CA-1120030-A

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_2ca2e4410855da087e11bf3eea8933fa
classificationCPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K38-00
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07K14-6555
classificationIPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K38-00
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07K14-575
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07K14-655
filingDate 1978-04-19-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1982-03-16-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f16c9db1f395ff3595114341f69f8ed5
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_5c31d7d9136c9b21cf67a8a74a7a9f4a
publicationDate 1982-03-16-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CA-1120030-A
titleOfInvention Somatostatin analogs and intermediates thereto
abstract Abstract of the Disclosure The tetradecapeptide D-Val-Gly-L-Cys-L-Lys-L-Asn-L-Phe-L-Phe-D-Trp-L-Lys-L-Thr-L-Phe-L-Thr-L-Ser-L-Cys-OH is described along with its corresponding non-toxic pharmaceutically-acceptable acid addition salts as well as intermediates useful in the synthesis of this tetradecapeptide. This tetradecapeptide is prepared by reacting the corresponding straight-chain tetradecapeptide with an oxidizing agent to con-vert the two sulfhydryl groups to a disulfide bridge. This tetradecapeptide as well as its pharmaceutically acceptable acid addition salts exhibit various activities including inhibition of the release of growth hormone and reduction of gut motility.
priorityDate 1977-04-21-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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