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filingDate 1992-08-14-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_bbb942b46e8db6e13daeb00957296ae9
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_3cb471105d2ea391c2e0937329079387
publicationDate 1994-03-08-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-H0665287-A
titleOfInvention peptide
abstract (57) [Summary] [Structure] A tetrapeptide in which the carboxyl group of the fourth amino acid Xaa from the N-terminus represented by Tyr-Pro-Ile-Xaa-NH 2 is amidated (wherein Xaa is Gln, An agent having opioid activity, which comprises Pro, Val or other amino acid) and salts thereof, and one or more of the tetrapeptides and salts thereof as an active ingredient. [Effects] Since the above-mentioned tetrapeptides and salts thereof have high opioid activity, analgesia, anesthesia, emotion, Respiratory, pulsation, body temperature, digestive tract function, feeding, immunity, secretion control of hormones such as insulin and somatostatin, promotion of absorption of electrolytes, and possibility of showing contraction control function of myocardium, It can be expected to be used as an analgesic anesthetic, a hypnotic, a gastrointestinal hormone secretagogue, an electrolyte absorption enhancer, and a diarrhea-improving agent by contraction of gastrointestinal transport muscles, and is particularly effective as an analgesic anesthetic and a sedative.
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type http://data.epo.org/linked-data/def/patent/Publication

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