934619-02-0Relevant articles and documents
Structure-activity relationships and blood distribution of antiplasmodial aminopeptidase-1 inhibitors
Deprez-Poulain, Rebecca,Flipo, Marion,Piveteau, Catherine,Leroux, Florence,Dassonneville, Sandrine,Florent, Isabelle,Maes, Louis,Cos, Paul,Deprez, Benoit
, p. 10909 - 10917 (2013/03/14)
Malaria is a severe infectious disease that causes between 655 000 and 1.2 million deaths annually. To overcome the resistance to current drugs, new biological targets are needed for drug development. Aminopeptidase M1 (PfAM1), a zinc metalloprotease, has
Novel selective inhibitors of the zinc plasmodial aminopeptidase PfA-M1 as potential antimalarial agents
Flipo, Marion,Beghyn, Terence,Leroux, Virginie,Florent, Isabelle,Deprez, Benoit P.,Deprez-Poulain, Rebecca F.
, p. 1322 - 1334 (2007/10/03)
Proteases that are expressed during the erythocytic stage of Plasmodium falciparum are newly explored drug targets for the treatment of malaria. We report here the discovery of potent inhibitors of PfA-M1, a metallo- aminopeptidase of the parasite. These