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Arch Pharm (Weinheim) ; 337(8): 434-9, 2004 Aug.
Article in English | MEDLINE | ID: mdl-15293262

ABSTRACT

The new and efficient synthesis of the title heterocyclic ring system is described starting from suitable 2-chloro-1, 8-naphthyridines. The synthesized 6H-indolo[2, 3-b][1, 8]naphthyridine derivatives were tested in vitro on 55 tumor cell lines for their anticancer properties. The presence of the acetylamino moiety at position 3 in the main ring system proved to be crucial for the cytostatic activity of this class of compounds.


Subject(s)
Antineoplastic Agents/chemical synthesis , Antineoplastic Agents/pharmacology , Indoles/chemical synthesis , Indoles/pharmacology , Naphthyridines/chemical synthesis , Naphthyridines/pharmacology , Cell Division/drug effects , Cell Line, Tumor , Drug Screening Assays, Antitumor , Humans , Indicators and Reagents , Magnetic Resonance Spectroscopy , Structure-Activity Relationship
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