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Bis-8-hydroxyquinoline and bis-8-hydroxyquinaldine N-substituted amines: A single methyl group structural difference between the two heterocycles, which modulates the antiproliferative effects

✍ Scribed by Sébastien Madonna; Aline Marcowycz; Delphine Lamoral-Theys; Gwendoline Van Goietsenoven; Jean Dessolin; Christine Pirker; Sabine Spiegl-Kreinecker; César-Alain Biraboneye; Walter Berger; Robert Kiss; Jean-Louis Kraus


Book ID
102343016
Publisher
Journal of Heterocyclic Chemistry
Year
2010
Tongue
English
Weight
114 KB
Volume
47
Category
Article
ISSN
0022-152X

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✦ Synopsis


Abstract

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The synthesis of a series of bis‐8‐hydroxyquinoline‐ and bis‐8‐hydroxyquinaldine‐substituted N‐benzyl or thiophenyl amines and their corresponding bis‐8‐hydroxyquinoline is reported. In vitro growth inhibitory effects of both series have been evaluated. It has been observed that analogs from the bis‐8‐hydroxyquinoline series exert nanomolar range activity, whereas the antiproliferative activity of the corresponding analogs from the bis‐8‐hydroxyquinaldine series was found to be drastically lower. Molecular docking and chemical–physical properties account for these observed growth inhibitory differences between the two series of analogs, which differ only by the presence of a methyl group at the 2 position of the heterocyclic ring. J. Heterocyclic Chem., (2010).


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