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Opioid receptor selectivity alteration by single residue replacement : synthesis and activity profile of [Dmt1]deltorphin B

Author
GUERRINI, R1 ; CAPASSO, A; SORRENTINO, L; ANACARDIO, R; BRYANT, S. D; LAZARUS, L. H; ATTILA, M; SALVADORI, S1
[1] Dipartimento di Scienze Farmaceutiche, Università di Ferrara, Via Fossato di Mortara 17 / 19, 44-100 Ferrara, Italy
Source

European journal of pharmacology. 1996, Vol 302, Num 1-3, pp 37-42 ; ref : 29 ref

CODEN
EJPHAZ
ISSN
0014-2999
Scientific domain
Pharmacology drugs
Publisher
Elsevier, Amsterdam
Publication country
Netherlands
Document type
Article
Language
English
Keyword (fr)
Activité biologique Agoniste Analgésique Animal In vitro In vivo Peptide opioïde Récepteur opiacé δ Récepteur opiacé μ Souris Synthèse peptidique Deltorphine dérivé Mammalia Rodentia Vertebrata
Keyword (en)
Biological activity Agonist Analgesic Animal In vitro In vivo Opioid peptide Opiate receptor δ Opiate receptor μ Mouse Peptide synthesis Mammalia Rodentia Vertebrata
Keyword (es)
Actividad biológica Agonista Analgésico Animal In vitro In vivo Péptido opioide Receptor opiáceo δ Receptor opiáceo μ Ratón Síntesis peptídica Mammalia Rodentia Vertebrata
Classification
Pascal
002 Biological and medical sciences / 002B Medical sciences / 002B02 Pharmacology. Drug treatments / 002B02B Neuropharmacology / 002B02B09 Neurotransmitters. Neurotransmission. Receptors / 002B02B09F Peptidergic system (neuropeptide, opioid peptide, opiates...). Adenosinergic and purinergic systems

Discipline
Pharmacological treatments
Origin
Inist-CNRS
Database
PASCAL
INIST identifier
3111090

Sauf mention contraire ci-dessus, le contenu de cette notice bibliographique peut être utilisé dans le cadre d’une licence CC BY 4.0 Inist-CNRS / Unless otherwise stated above, the content of this bibliographic record may be used under a CC BY 4.0 licence by Inist-CNRS / A menos que se haya señalado antes, el contenido de este registro bibliográfico puede ser utilizado al amparo de una licencia CC BY 4.0 Inist-CNRS

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