Natural product-inspired aryl isonitriles as a new class of antimalarial compounds against drug-resistant parasites

被引:5
|
作者
Kyei-Baffour, Kwaku [1 ,2 ]
Davis, Dexter C. [1 ,2 ]
Boskovic, Zarko [4 ]
Kato, Nobutaka [3 ]
Dai, Mingji [1 ,2 ]
机构
[1] Purdue Univ, Dept Chem, W Lafayette, IN 47907 USA
[2] Purdue Univ, Ctr Canc Res, W Lafayette, IN 47907 USA
[3] Broad Inst Harvard & MIT, 415 Main St, Cambridge, MA 02142 USA
[4] Univ Kansas, Dept Med Chem, Lawrence, KS 66045 USA
关键词
Isonitrile; Antimalarial; Drug resistance; Natural product; Terpene Isonitrile; Stilbene; Drug discovery; KALIHINOL; SPONGE; SESQUITERPENES; ARTEMISININ;
D O I
10.1016/j.bmc.2020.115678
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
Malaria is a prevalent and deadly disease. The fast emergence of drug-resistant malaria parasites makes the situation even worse. Thus, developing new chemical entities, preferably with novel mechanisms of action, is urgent and important. Inspired by the complex and scarce isonitrile-containing terpene natural products, we evaluated a collection of easily prepared synthetic mono- and bis-isonitrile compounds, most of which feature a simple, but rigid stilbene backbone. From this collection, potent antimalarial lead compounds with EC50 value ranging from 27 to 88 nM against the Dd2 strain using a blood stage proliferation assay were identified. Preliminary SAR information showed that the isonitrile group is essential for the observed activity against the Dd2 strain and the bis-isonitrile compounds in general perform better than the corresponding mono-isonitrile compounds.
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页数:4
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