Synthesis, structure, and cytostatic properties of new olivacine derivatives
- Author
- JASZTOLD-HOWORKO, Ryszard1 ; CROISY, Alain2 ; CARREZ, Daniele2 ; JAROSZEWICZ, Iwona3 ; NASULEWICZ, Anna3 ; PELCZYNSKA, Marzena3 ; OPOLSKI, Adam3
[1] Wrocław University of Medicine, Faculty of Pharmacy, Department of Organic Chemistry, Wrocław, Poland
[2] Institut Curie Recherche, Orsay, France
[3] Institute of Immunology and Experimental Therapy, Polish Academy of Sciences, Wrocław, Poland - Source
Archiv der Pharmazie (Weinheim). 2004, Vol 337, Num 11, pp 599-604, 6 p ; ref : 7 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
- 1-Substituted-6H-pyrido[4,3-b]carbazole Cytotoxicity Olivacine
- Keyword (fr)
- Activité biologique Animal Anticancéreux Cytotoxicité In vitro Lignée L1210 Lignée cellulaire Souris Synthèse chimique Olivacine dérivé Pyrido[4,3-b]carbazole dérivé Pyridocarbazole Mammalia Rodentia Vertebrata
- Keyword (en)
- Biological activity Animal Antineoplastic agent Cytotoxicity In vitro L1210 cell line Cell line Mouse Chemical synthesis Mammalia Rodentia Vertebrata
- Keyword (es)
- Actividad biológica Animal Anticanceroso Citotoxicidad In vitro Célula L1210 Línea celular Ratón Síntesis química Mammalia Rodentia Vertebrata
- 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
- 16318213
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.200400893 
https://dx.doi.org/10.1002/ardp.200400893
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