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Synthesis and benzodiazepine receptor activity of some 4,5-dihydro-1H-pyrazolo [4,3-c] [1,8] naphthyridine derivatives

Author
DA SETTIMO, A1 ; PRIMOFIORE, G1 ; DA SETTIMO, F1 ; SIMORINI, F1 ; BARILI, P. L; SENATORE, G; MARTINI, C; LUCACCHINI, A
[1] Univ. Pisa, ist. chimica farmaceutica tossicologica, 56126 Pisa, Italy
Source

Drug design and discovery (Print). 1994, Vol 11, Num 4, pp 307-328 ; ref : 49 ref

CODEN
DDDIEV
ISSN
1055-9612
Scientific domain
Pharmacology drugs
Publisher
Harwood Academic Publishers, Amsterdam
Publication country
Netherlands
Document type
Article
Language
English
Keyword (fr)
Affinité Animal Bovin Encéphale Fixation ligand In vitro Naphtyridine dérivé Relation structure activité Récepteur benzodiazépinique Synthèse chimique Système nerveux central Artiodactyla Mammalia Ungulata Vertebrata
Keyword (en)
Affinity Animal Bovine Brain (vertebrata) Ligand binding In vitro Naphtyridine derivatives Structure activity relation Benzodiazepine receptor Chemical synthesis Central nervous system Artiodactyla Mammalia Ungulata Vertebrata
Keyword (es)
Afinidad Animal Bovino Encéfalo Fijación ligando In vitro Relación estructura actividad Receptor benzodiazepínico Síntesis química Sistema nervioso central Artiodactyla Mammalia Ungulata Vertebrata
Classification
Pascal
002 Biological and medical sciences / 002B Medical sciences / 002B02 Pharmacology. Drug treatments / 002B02B Neuropharmacology / 002B02B09 Neurotransmitters. Neurotransmission. Receptors / 002B02B09D Gabaergic and benzodiazepinic system

Discipline
Pharmacological treatments
Origin
Inist-CNRS
Database
PASCAL
INIST identifier
4180564

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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