Dechy-Cabaret Odile, Benoit-Vical Françoise, Loup Christophe, Robert Anne, Gornitzka Heinz, Bonhoure Anne, Vial Henri, Magnaval Jean-François, Séguéla Jean-Paul, Meunier Bernard
Laboratoire de Chimie de Coordination du CNRS, 205 route de Narbonne, 31077 Toulouse Cedex 4, France.
Chemistry. 2004 Apr 2;10(7):1625-36. doi: 10.1002/chem.200305576.
Trioxaquines are dual molecules that contain a trioxane motif linked to an aminoquinoline entity. Among the different compounds of this series, trioxaquine cis-15 (DU1302 c), prepared from alpha-terpinene, a cheap natural product, showed efficient antimalarial activity in vitro on both sensitive and resistant strains of Plasmodium falciparum (IC(50)=5-19 nM). A stereochemical description of this stable, nontoxic, and non-genotoxic antimalarial agent is detailed. Mice infected with P. vinckei were successfully treated with cis-15 in a four-day suppressive test. The doses required to decrease parasitemia by 50 % (ED(50)) were 5 and 18 mg kg(-1) d(-1) after intraperitoneal and oral administration, respectively. Parasitemia clearance was complete without recrudescence at an intraperitoneal dose of 20 mg kg(-1) d(-1).
三氧喹啉是一类双分子化合物,其包含一个与氨基喹啉实体相连的三恶烷结构单元。在该系列的不同化合物中,由廉价天然产物α-萜品烯制备的三氧喹啉顺式-15(DU1302 c),在体外对恶性疟原虫的敏感株和耐药株均表现出高效的抗疟活性(IC(50)=5-19 nM)。本文详细描述了这种稳定、无毒且无遗传毒性的抗疟药物的立体化学结构。在一项为期四天的抑制试验中,感染文氏疟原虫的小鼠经顺式-15成功治疗。腹腔注射和口服给药后,使疟原虫血症降低50%所需的剂量(ED(50))分别为5和18 mg kg(-1) d(-1)。腹腔注射剂量为20 mg kg(-1) d(-1)时,疟原虫血症得以完全清除且无复发。