Literature DB >> 15293262

Synthesis and cytostatic properties of some 6H-Indolo[2, 3-b][1, 8]naphthyridine derivatives.

Henryk Mastalarz1, Ryszard Jasztold-Howorko, Felicja Rulko, Alain Croisy, Daniele Carrez.   

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.

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Year:  2004        PMID: 15293262     DOI: 10.1002/ardp.200200696

Source DB:  PubMed          Journal:  Arch Pharm (Weinheim)        ISSN: 0365-6233            Impact factor:   3.751


  1 in total

1.  Synthesis and structure-activity relationship studies of novel 3,9-substituted α-carboline derivatives with high cytotoxic activity against colorectal cancer cells.

Authors:  Yi-Chien Lin; Yi-Fong Chen; Li-Shin Tseng; Yueh-Hsuan Lee; Susan L Morris-Natschke; Sheng-Chu Kuo; Ning-Sun Yang; Kuo-Hsiung Lee; Li-Jiau Huang
Journal:  Eur J Med Chem       Date:  2016-01-07       Impact factor: 6.514

  1 in total

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