Bioorganic and Medicinal Chemistry Letters p. 5988 - 5992 (2006)
Update date:2022-08-02
Topics:
Moret, Vincent
Dereudre-Bosquet, Nathalie
Clayette, Pascal
Laras, Younes
Pietrancosta, Nicolas
Rolland, Amandine
Weck, Clement
Marc, Sylvain
Kraus, Jean-Louis
To find new derivatives that block different virus strains entry in cells bearing specific surface receptors represent an interesting challenge for medicinal chemists. Here, we report the synthesis and the anti-HIV properties of a new series of analogues based on the introduction of quinoline moiety on various polyamine backbones, including polyazamacrocycles. Three compounds 7, 8, and 10 of this series were found active on PBMCs cells infected by HIV-1 LAV or by HIV-1 BaL, in contrast the well-known reference compound 1a (AMD 3100) was found only active on HIV-1 LAV strain.
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