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Structure-activity relationship of N17'-substituted norbinaltorphimine congeners. Role of the N17' basic group in the interaction with a putative address subsite on the κ opioid receptor

Author
PORTOGHESE, P. S; LIN, C.-E; FAROUZ-GRANT, F; TAKEMORI, A. E
Univ. Minnesota, coll. pharmacy, dep. medicinal chemistry, Minneapolis MN 55455, United States
Source

Journal of medicinal chemistry (Print). 1994, Vol 37, Num 10, pp 1495-1500 ; ref : 30 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 Analyse structurale Antagoniste Position Relation structure activité Récepteur opiacé κ Site actif Structure moléculaire Substitution chimique Synthèse chimique Norbinaltorphimine
Keyword (en)
Biological activity Analog Structural analysis Antagonist Position Structure activity relation Opiate receptor κ Active site Molecular structure Chemical substitution Chemical synthesis
Keyword (es)
Actividad biológica Análogo Análisis estructural Antagonista Posición Relación estructura actividad Receptor opiáceo κ Lugar activo Estructura molecular Sustitución química 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
4131481

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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