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Preparation and pharmacological activities of spiro[3,4-dihydro-6/7-R-1,2,4-benzotriazine-3,4'-(1'-substituted)piperidines]

Author
NOVELLI, F1 ; SPARATORE, F1
[1] Istituto di Scienze Farmaceutiche, Università di Genova, Viale Benedetto XV 3, 16132 Genova, Italy
Source

Il Farmaco (Pavia). 1996, Vol 51, Num 8-9, pp 541-550 ; ref : 36 ref

ISSN
0014-827X
Scientific domain
Pharmacology drugs
Publisher
Elsevier Science, Lausanne
Publication country
Switzerland
Document type
Article
Language
English
Keyword (fr)
Antagoniste Antiallergique Antihypertenseur Antiinflammatoire Cholestérol Composé aromatique Composé tricyclique Hypolipémiant Hétérocycle azote In vitro In vivo Pipéridine dérivé Récepteur α-adrénergique Spirane Synthèse chimique Test activité Benzotriazine dérivé Spiro[1,2,4-Benzotriazine-3:4p-pipéridine](3,4-dihydro-1p-[3-(4-fluorobenzoyl)propyl])
Keyword (en)
Antagonist Antiallergic Antihypertensive agent Antiinflammatory agent Cholesterol Aromatic compound Tricyclic compound Antilipemic agent Nitrogen heterocycle In vitro In vivo Piperidine derivatives α-Adrenergic receptor Spiran Chemical synthesis Screening test
Keyword (es)
Antagonista Antialérgico Antihipertensivo Antiinflamatorio Colesterol Compuesto aromático Compuesto tricíclico Hipolipemiante Heterociclo nitrógeno In vitro In vivo Piperidina derivado Receptor α-adrenérgico Espirano Síntesis química Prueba actividad
Classification
Pascal
002 Biological and medical sciences / 002B Medical sciences / 002B02 Pharmacology. Drug treatments / 002B02N General and cellular metabolism. Vitamins

Discipline
Pharmacological treatments
Origin
Inist-CNRS
Database
PASCAL
INIST identifier
3249157

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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