Falcipain Inhibitors Based on the Natural Product Gallinamide A are Potent in vitro and in vivo Antimalarials

A library of analogues of the cyanobacterium-derived depsipeptide natural product gallinamide A were designed and prepared using a highly efficient and convergent synthetic route. Analogues were shown to exhibit potent inhibitory activity against the Plasmodium falciparum cysteine proteases falcipain 2 (FP2) and falcipain 3 (FP3) and against cultured chloroquine-sensitive (3D7) and chloroquine-resistant (W2) strains of P. falciparum. Three lead compounds were selected for evaluation of in vivo efficacy against Plasmodium berghei infection in mice based on their improved blood, plasma and microsomal stability profiles compared to the parent natural product. One of the lead analogues cured P. berghei-infected mice in the Peters-4-day-suppressive test when administered 25 mg/kg intraperitoneally daily for four days. The compound was also capable of clearing parasites in established infections at 50 mg/kg intraperitoneally daily for four days and exhibited moderate activity when administered as four oral dose...