New hydrazones of 5-nitro-2-furaldehyde with adamantanealkanohydrazides: synthesis and in vitro trypanocidal activity

被引:16
作者
Foscolos, Angeliki-Sofia [1 ]
Papanastasiou, Ioannis [1 ]
Foscolos, George B. [1 ]
Tsotinis, Andrew [1 ]
Kellici, Tahsin F. [2 ,4 ]
Mavromoustakos, Thomas [2 ]
Taylor, Martin C. [3 ]
Kelly, John M. [3 ]
机构
[1] Univ Athens, Fac Pharm, Sch Hlth Sci, Dept Pharmaceut Chem, Athens 15784, Greece
[2] Univ Athens, Dept Organ Chem, Fac Chem, Athens 15771, Greece
[3] London Sch Hyg & Trop Med, Dept Pathogen Mol Biol, London WC1 E7HT, England
[4] Univ Ioannina, Fac Chem, Dept Organ Chem & Biochem, GR-45110 Ioannina, Greece
基金
英国惠康基金;
关键词
MIT UROTROPIN-STRUKTUR; AFRICAN TRYPANOSOMIASIS; MOLECULAR-DYNAMICS; RESISTANCE; CHEMOTHERAPY; BENZNIDAZOLE; MELARSOPROL; NIFURTIMOX; THERAPY;
D O I
10.1039/c6md00035e
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Nifurtimox, a hydrazone of 5-nitro-2-furaldehyde is used therapeutically against Trypanosoma brucei and Trypanosoma cruzi infections. Exploiting our previous observation that adamantane derivatives display trypanocidal activity, we designed and synthesised a range of hydrazones of 5-nitro-2-furaldehyde with adamantane alkanohydrazides. The most promising compounds had >20 times greater activity (IC50 similar to 100 nM) than nifurtimox, with selectivity indices of 20-80. SAR studies revealed that activity is associated with increased lipophilicity and influenced by conformational flexibility. Derivatives lacking a nitro group were practically inactive against both parasites. The approaches described demonstrate the feasibility of enhancing the potency of chemical entities with known trypanocidal activity.
引用
收藏
页码:1229 / 1236
页数:8
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