Synthesis and cytostatic properties of some 6H-indolo[2,3-b][1,8]naphthyridine derivatives
- Author
- MASTALARZ, Henryk1 ; JASZTOLD-HOWORKO, Ryszard1 ; RULKO, Felicja1 ; CROISY, Alain2 ; CARREZ, Daniele2
[1] Department of Organic Chemistry, University of Medicine, Wrocław, Poland
[2] Institut Curie, Section de Biologie, INSERM U-350, Orsay, France - Source
Archiv der Pharmazie (Weinheim). 2004, Vol 337, Num 8, pp 434-439, 6 p ; ref : 6 ref
- CODEN
- ARPMAS
- ISSN
- 0365-6233
- Scientific domain
- Organic chemistry; Pharmacology drugs
- Publisher
- Wiley-VCH, Weinheim
- Publication country
- Germany
- Document type
- Article
- Language
- English
- Author keyword
- 6H-lndolo[2,3-b][1,8]naphthyridines Cytotoxicity Synthesis
- Keyword (fr)
- Anticancéreux Cellule tumorale Composé aromatique Composé tétracyclique Cytotoxicité Hétérocycle azote In vitro Lignée cellulaire Relation structure activité Synthèse chimique Indolo[2,3-b][1,8]naphtyridine dérivé Indolonaphtyridine
- Keyword (en)
- Antineoplastic agent Tumor cell Aromatic compound Tetracyclic compound Cytotoxicity Nitrogen heterocycle In vitro Cell line Structure activity relation Chemical synthesis
- Keyword (es)
- Anticanceroso Célula tumoral Compuesto aromático Compuesto tetracíclico Citotoxicidad Heterociclo nitrógeno In vitro Línea celular Relación estructura actividad Síntesis química
- Classification
- Pascal
- 002 Biological and medical sciences / 002B Medical sciences / 002B02 Pharmacology. Drug treatments / 002B02R Antineoplastic agents / 002B02R01 General aspects
- Discipline
- Pharmacological treatments
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- 16019810
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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DOI
10.1002/ardp.200200696 
https://dx.doi.org/10.1002/ardp.200200696
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