作者
Christoph Boss,Hamed Aissaoui,Nathalie Amaral,Aude Bauer,Stephanie Bazire,Christoph A. Binkert,Reto Brun,Cédric Bürki,Claire‐Lise Ciana,Olivier Corminboeuf,Stéphane Delahaye,Claire Dollinger,Christoph Fischli,Walter Fischli,Alexandre Flock,Marie‐Céline Frantz,Malory Girault,Corinna Grisostomi,Astrid Friedli,Bibia Heidmann,Claire Hinder,Gaël Jacob,Amélie Le Bihan,Sophie Malrieu,Saskia Mamzed,Aurelien Merot,Solange Meyer,Sabrina Peixoto,Nolwenn Petit,Romain Siegrist,Julien Trollux,Thomas Weller,Sergio Wittlin
摘要
More than 40 % of the world's population is at risk of being infected with malaria. Most malaria cases occur in the countries of sub-Saharan Africa, Central and South America, and Asia. Resistance to standard therapy, including artemisinin combinations, is increasing. There is an urgent need for novel antimalarials with new mechanisms of action. In a phenotypic screen, we identified a series of phenylalanine-based compounds that exhibit antimalarial activity via a new and yet unknown mechanism of action. Our optimization efforts culminated in the selection of ACT-451840 [(S,E)-N-(4-(4-acetylpiperazin-1-yl)benzyl)-3-(4-(tert-butyl)phenyl)-N-(1-(4-(4-cyanobenzyl)piperazin-1-yl)-1-oxo-3-phenylpropan-2-yl)acrylamide] for clinical development. Herein we describe our optimization efforts from the screening hit to the potential drug candidate with respect to antiparasitic activity, drug metabolism and pharmacokinetics (DMPK) properties, and in vivo pharmacological efficacy.