A new class of anthelmintics effective against drug-resistant nematodes

被引:374
|
作者
Kaminsky, Ronald [1 ]
Ducray, Pierre [2 ]
Jung, Martin [1 ]
Clover, Ralph [3 ]
Rufener, Lucien [1 ,4 ]
Bouvier, Jacques [1 ]
Weber, Sandra Schorderet [1 ]
Wenger, Andre [1 ]
Wieland-Berghausen, Susanne [2 ]
Goebel, Thomas [2 ]
Gauvry, Noelle [2 ]
Pautrat, Francois [2 ]
Skripsky, Thomas [2 ]
Froelich, Olivier [1 ]
Komoin-Oka, Clarisse
Westlund, Bethany [3 ]
Sluder, Ann [3 ]
Maeser, Pascal [4 ]
机构
[1] Novartis Ctr Rech Sante Animale, CH-1566 St Aubin, Switzerland
[2] Novartis Anim Hlth Inc, CH-4002 Basel, Switzerland
[3] Cambria Biosci, Woburn, MA 01801 USA
[4] Lab Cent Vet Bingerville, Lanada, Cote Ivoire
关键词
D O I
10.1038/nature06722
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Anthelmintic resistance in human and animal pathogenic helminths has been spreading in prevalence and severity to a point where multidrug resistance against the three major classes of anthelmintics - the benzimidazoles, imidazothiazoles and macrocyclic lactones - has become a global phenomenon in gastrointestinal nematodes of farm animals. Hence, there is an urgent need for an anthelmintic with a new mode of action. Here we report the discovery of the amino- acetonitrile derivatives ( AADs) as a new chemical class of synthetic anthelmintics and describe the development of drug candidates that are efficacious against various species of livestock- pathogenic nematodes. These drug candidates seem to have a novel mode of action involving a unique, nematode- specific clade of acetylcholine receptor subunits. The AADs are well tolerated and of low toxicity to mammals, and overcome existing resistances to the currently available anthelmintics.
引用
收藏
页码:176 / U19
页数:6
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