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publicationDate 1982-05-01-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber ES-8204412-A1
titleOfInvention PROCEDURE FOR OBTAINING A CYCLIC OCTAPEPTIDE
abstract PROCEDURE FOR OBTAINING A CYCLIC OCTAPEPTIDE, AS WELL AS ITS COMPLEXES AND SALTS, OF FORMULA (I), IN WHICH L-TRP, D-TRP OR AN ANALOGUE WITH A HALOGEN IN THE INDOLIC NUCLEUS; AC IS HYDROGEN OR ACYL; A IS L-PHE, D-PHE, L-PHG, WITH THE PHENILIC RING REPLACED AND WITHOUT SUBSTITUTE OR SATURATED; AND B IS A RADICAL OF AMINOCARBOXYL ACID. CONSISTS OF THE DISSOLUTION OF THE PROTECTIVE GROUP (S) OF A CYCLICAL COMPOUND STRUCTURALLY CORRESPONDING TO THE OCTAPEPTIDE TO BE OBTAINED, IN WHICH AT LEAST ONE OF THE AMINO, HYDROXYL AND / OR CARBOXYL GROUPS LEADS AN ADDITIONAL PROTECTIVE GROUP. THE DISSOCIATION REACTION IS CARRIED OUT ACCORDING TO CONVENTIONAL METHODS DEPENDING ON THE TYPE OF GROUP TO BE SEPARATED. FROM THE COMPOUND OBTAINED, THE CORRESPONDING SALT, ACID, BASE OR COMPLEX CAN BE OBTAINED. THESE COMPOUNDS HAVE PHARMACOLOGICAL APPLICATIONS FOR THEIR PROPERTIES OF INHIBITING THE SECRETION REGULATED BY THE HYPOPHYSIS OF THE GROWTH HORMONE AND THE SECRETORY ACTIVITY OF THE PANCREASANDOCRINE.
priorityDate 1979-12-21-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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