Synthesis and Biological Properties of New Benz[h]isoquinoline Derivatives
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概要
- 論文の詳細を見る
In order to determine the importance of the pyrrolic nitrogen atom in a series of suitably substituted γ-carbolines derivatives for their cytotoxic and antitumor properties, a series of structurally related benz[h]isoquinolines were synthesized. When compared to the "parent" γ-carbolines, these new compounds showed greatly decreased effects on topoisomerases I and II. Whereas the 8-hydroxylated derivatives retained a significant cytotoxicity, all the new compounds were devoid of antitumor effect in the P388 murine ip-ip system.
- 公益社団法人日本薬学会の論文
- 1994-04-15
著者
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Riou Jean-francois
Rhone-poulenc Rorer S. A. Centre De Recherche De Vitry-alfortville
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Bisagni E
Inst. Curie Rech. Cnrs Orsay Fra
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JANIN Yves
URA 1387 CNRS, Institut Curie Section de Biologie Bat. 110 Centre Universitaire
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CARREZ Daniele
U 350 INSERM, Institut Curie Section de Biologie Bat. 110 Centre Universitaire
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BISAGNI Emile
URA 1387 CNRS, Institut Curie Section de Biologie Bat. 110 Centre Universitaire
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Janin Yves
Ura 1387 Cnrs Institut Curie Section De Biologie Bat. 110 Centre Universitaire
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Carrez Daniele
U 350 Inserm Institut Curie Section De Biologie Bat. 110 Centre Universitaire