Title of article :
Synthesis and biological evaluation of 7-azaindolocarbazoles
Author/Authors :
Sylvain Routier، نويسنده , , Nathalie Ayerbe، نويسنده , , Jean-Yves Mérour، نويسنده , , Gérard Coudert، نويسنده , , Christian Bailly، نويسنده , , Alain Pierré، نويسنده , , Bruno Pfeiffer، نويسنده , , Daniel-Henri Caignard، نويسنده , , Pierre Renard، نويسنده ,
Issue Information :
هفته نامه با شماره پیاپی سال 2002
Pages :
10
From page :
6621
To page :
6630
Abstract :
In the course of a program aimed at designing antitumor agents containing an indolocarbazole framework, an efficient synthetic scheme based on the use of 3,4-dibromo-N-methylmaleimide and 7-azaindole has been developed to elaborate a series of mono- and di-aza derivatives of arcyriaflavin. The procedure was further exploited to introduce a hydroxyl group at different positions on the indole moiety of the non-symmetrical compounds. The DNA binding capacity and cytotoxic potential of these 7-azaindolocarbazole derivatives was evaluated.
Keywords :
indolocarbazole , 7-Azaindole , Synthesis
Journal title :
Tetrahedron
Serial Year :
2002
Journal title :
Tetrahedron
Record number :
1083354
Link To Document :
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