期刊
EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY
卷 120, 期 -, 页码 353-362出版社
ELSEVIER FRANCE-EDITIONS SCIENTIFIQUES MEDICALES ELSEVIER
DOI: 10.1016/j.ejmech.2016.04.064
关键词
Nitroimidazole; Antiparasitic agent; Giardia lamblia; Entamoeba histolytica; Plasma protein binding; Metabolism
资金
- UQ CIEF
- NHMRC [AP1063214]
- NIH [AI114671, DE020607]
- Australian Postgraduate Award (APA)
- QLD Government Smart Futures PhD scholarship
- Wellcome Trust Seeding Drug Discovery Award [094977/Z/10/Z]
- Wellcome Trust Strategic Award [066648 CO-ADD]
- NHMRC Fellowships [AF511105, APP1059354]
- IMB scholarship
Diarrhoeal diseases caused by the intestinal parasites Giardia lamblia and Entamoeba histolytica constitute a major global health burden. Nitroimidazoles are first-line drugs for the treatment of giardiasis and amebiasis, with metronidazole 1 being the most commonly used drug worldwide. However, treatment failures in giardiasis occur in up to 20% of cases and development of resistance to metronidazole is of concern. We have re-examined 'old' nitroimidazoles as a foundation for the systematic development of next-generation derivatives. Using this approach, derivatisation of the nitroimidazole carboxamide scaffold provided improved antiparasitic agents. Thirty-three novel nitroimidazole carboxamides were synthesised and evaluated for activity against G. lamblia and E. histolytica. Several of the new compounds exhibited potent activity against G. lamblia strains, including metronidazole-resistant strains of G. lamblia (EC50 = 0.1-2.5 mu M cf. metronidazole EC50 = 6.1-18 mu M). Other compounds showed improved activity against E. histolytica (EC50 = 1.7-5.1 mu M cf. metronidazole EC50 = 5.0 mu M), potent activity against Trichomonas vaginalis (EC50 = 0.6-1.4 mu M cf. metronidazole EC50 = 0.8 mu M) and moderate activity against the intestinal bacterial pathogen Clostridium difficile (0.5-2 mu g/mL, cf. metronidazole = 0.5 mu g/mL). The new compounds had low toxicity against mammalian kidney and liver cells (CC50 > 100 mu M), and selected antiparasitic hits were assessed for human plasma protein binding and metabolic stability in liver microsomes to demonstrate their therapeutic potential. (C) 2016 The Authors. Published by Elsevier Masson SAS.
作者
我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。
推荐
暂无数据