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Synthesis of naltrexone-derived δ-opioid antagonists. Role of conformation of the δ adress moiety

Author
PORTOGHESE, P. S; SULTANA, M; MOE, S. T; TAKEMORI, A. E
Univ. Minnesota, coll. pharmacy, dep. medicinal, Minneapolis MN 55455, United States
Source

Journal of medicinal chemistry (Print). 1994, Vol 37, Num 5, pp 579-585 ; ref : 31 ref

CODEN
JMCMAR
ISSN
0022-2623
Scientific domain
Pharmacology drugs
Publisher
American Chemical Society, Washington, DC
Publication country
United States
Document type
Article
Language
English
Keyword (fr)
Activité biologique Analogue Animal Antagoniste analgésique narcotique Antagoniste Benzène Composé aromatique Conformation Fixation biologique In vitro In vivo Indole dérivé Muscle lisse Naltrexone Récepteur opiacé δ Synthèse chimique
Keyword (en)
Biological activity Analog Animal Narcotic antagonist Antagonist Benzene Aromatic compound Conformation Biological fixation In vitro In vivo Indole derivatives Smooth muscle Opiate receptor δ Chemical synthesis
Keyword (es)
Actividad biológica Análogo Animal Antagonista narcótico Antagonista Benceno Compuesto aromático Conformación Fijación biológica In vitro In vivo Indol derivado Músculo liso Receptor opiáceo δ Síntesis química
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
3980192

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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