Synthesis of totarol amino alcohol derivatives and their antiplasmodial activity and cytotoxicity

被引:45
作者
Clarkson, C
Musonda, CC
Chibale, K [1 ]
Campbell, WE
Smith, P
机构
[1] Univ Cape Town, Dept Chem, ZA-7701 Rondebosch, South Africa
[2] Univ Cape Town, Groote Schuur Hosp, Dept Med, Div Pharmacol, ZA-7925 Observatory, South Africa
基金
英国医学研究理事会;
关键词
D O I
10.1016/S0968-0896(03)00491-7
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
The previously unknown antiplasmodial activity of the plant derived natural product totarol is reported. Novel beta-amino alcohol derivatives based on this natural product were designed, synthesised and evaluated for in vitro anti plasmodia I activity and cytotoxicity. These derivatives showed antiplasmodial IC50 values in the range of 0.6-3.0 muM and were equally active against a chloroquine-sensitive and resistant strain of Plasmodium falciparum, while showing little cytotoxicity against a mammalian cell line (CHO). In terms of lead development, two of the compounds based on substituted phenylpiperazine warrant further investigation as potential antiplasmodial leads. In addition to their selective antiplasmodial activity and lack of chloroquine cross-resistance, these compounds are structurally different to any of the available antimalarial drugs. (C) 2003 Elsevier Ltd. All rights reserved.
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页码:4417 / 4422
页数:6
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