http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-4309343-A

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classificationCPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K38-00
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07K14-702
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07K5-1016
classificationIPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K38-00
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07K5-107
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07K14-70
filingDate 1980-11-25-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1982-01-05-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_8330ab377fbb6ad884e22d0b004f1db0
publicationDate 1982-01-05-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-4309343-A
titleOfInvention Pharmacologically active peptides
abstract Compounds of the formula [R-Tyr-A-Gly-(N-R1)Phe(p-Y)-X]2-(CH2)n in which R is hydrogen or methyl; A is the residue of a D-amino acid selected from the group consisting of Ala, Abu, Ser, Thr, and Met; R1 is hydrogen, C1-C3 primary alkyl, cyclopropylmethyl, or allyl; Y is hydrogen or fluoro; n is an integer from 1 to 10; and X is -NH- or a group of the formula <IMAGE> in which R2 is hydrogen or C1-C3 primary alkyl; R3 is phenyl, 2-methylthioethyl, or isobutyl; or R2 and R3 taken together are -CH2-CH2-CH2-; subject to the limitation that, when R2 is other than hydrogen, R1 is hydrogen; are useful analgesic agents.
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