Miltefosine - discovery of the antileishmanial activity of phospholipid derivatives

被引:120
作者
Croft, Simon L. [1 ]
Engel, Juergen
机构
[1] DNDi, 1 Pl St Gervais, CH-1201 Geneva, Switzerland
[2] Zentaris GmbH, D-60314 Frankfurt, Germany
关键词
leishmaniasis; antileishmanial; miltefosine; alkyl-phosphocholines; anticancer drug;
D O I
10.1016/j.trstmh.2006.03.009
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 [公共卫生与预防医学]; 120402 [社会医学与卫生事业管理];
摘要
Miltefosine (hexadecylphosphocholine, Impavido (TM)), a novel antiprotozoal drug used for the treatment of visceral and cutaneous leishmaniasis, was identified and evaluated independently in the early 1980s as a potential anticancer drug in Germany and as an antileishmanial drug in the UK. Although miltefosine is not the most active compound of its class against Leishmania parasites in vitro, the early demonstration of activity after oral administration in experimental models of visceral leishmaniasis helped to bring this compound to the attention of WHO TDR for further development in a unique collaboration model-with the pharmaceutical industry (Zentaris GmbH). Miltefosine is active against most Leishmania species, including those that cause cutaneous disease. (c) 2006 Royal Society of Tropical Medicine and Hygiene. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:S4 / S8
页数:5
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