Floxacrine analog WR 243251 inhibits hematin polymerization

被引:15
作者
Dorn, A
Scovill, JP
Ellis, WY
Matile, H
Ridley, RG
Vennerstrom, JL
机构
[1] Univ Nebraska, Med Ctr, Coll Pharm, Omaha, NE 68198 USA
[2] F Hoffmann La Roche & Co Ltd, Preclin Res, Div Pharma, CH-4070 Basel, Switzerland
[3] Walter Reed Army Med Ctr, Walter Reed Army Inst Res, Div Expt Therapeut, Washington, DC 20307 USA
关键词
D O I
10.4269/ajtmh.2001.65.19
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
Floxacrine was a promising antimalarial compound that led to the identification of WR 243251. On the basis of their structures, we suspected that these compounds might be good inhibitors of hematin polymerization. Indeed, WR 243251 was as potent and floxacrine was only 2-fold less potent than chloroquine as inhibitors of this process. However. this hematin polymerization inhibition did not completely account for the increased antimalarial potency of WR 243251 versus chloroquine. The WR 243251 ketone hydrolysis product WR 243246 was without activity against hematin polymerization. These data also confirm that hematin polymerization inhibition can be quite sensitive to small changes in inhibitor structure.
引用
收藏
页码:19 / 20
页数:2
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