Design and synthesis of hydroxyferroquine derivatives with antimalarial and antiviral activities

被引:223
作者
Biot, C
Daher, W
Chavain, N
Fandeur, T
Khalife, J
Dive, D
De Clercq, E
机构
[1] USTL, Unite Catalyse & Chim Solide, ENSCL, CNRS,UMR 8181, F-59652 Villeneuve Dascq, France
[2] Inst Pasteur, INSERM, U547, F-59019 Lille, France
[3] UMR Univ, INRA Immunol Parasitaire, Fac Pharmaceut Sci, F-37200 Tours, France
[4] Katholieke Univ Leuven, Rega Inst Med Res, B-3000 Louvain, Belgium
关键词
D O I
10.1021/jm0601856
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Three ferroquine (FQ) derivatives, closely mimicking the antimalarial drug hydroxychloroquine (HCQ), have been prepared. Whereas these organometallic compounds provide the expected reduced cytotoxic effects compared to FQ, they inhibit in vitro growth of Plasmodium falciparum far better than chloroquine (CQ). Moreover, this new class of bioorganometallic compounds exert antiviral effects with some selectivity toward SARS-CoV infection. These new drugs may offer an interesting alternative for Asia where SARS originated and malaria has remained endemic.
引用
收藏
页码:2845 / 2849
页数:5
相关论文
共 34 条
[1]   INVITRO ASSESSMENT OF THE ANTIMALARIAL ACTIVITY OF CHLOROQUINE AND ITS MAJOR METABOLITES [J].
ADEROUNMU, AF .
ANNALS OF TROPICAL MEDICINE AND PARASITOLOGY, 1984, 78 (06) :581-585
[2]   Current drug development portfolio for antimalarial therapies [J].
Biagini, GA ;
O'Neill, PM ;
Bray, PG ;
Ward, SA .
CURRENT OPINION IN PHARMACOLOGY, 2005, 5 (05) :473-478
[3]   Synthesis and antimalarial activity in vitro of potential metabolites of ferrochloroquine and related compounds [J].
Biot, C ;
Delhaes, L ;
N'Diaye, CM ;
Maciejewski, LA ;
Camus, D ;
Dive, D ;
Brocard, JS .
BIOORGANIC & MEDICINAL CHEMISTRY, 1999, 7 (12) :2843-2847
[4]  
Biot C., 2004, CURR MED CHEM, V3, P135, DOI DOI 10.2174/1568012043354008
[5]  
BIOT C, 2006, IN PRESS CURR DRUG T
[6]   Insights into the mechanism of action of ferroquine. Relationship between physicochemical properties and antiplasmodial activity [J].
Biot, Christophe ;
Taramelli, Donatella ;
Forfar-Bares, Isabelle ;
Maciejewski, Lucien A. ;
Boyce, Mlandzeni ;
Nowogrocki, Guy ;
Brocard, Jacques S. ;
Basilico, Nicoletta ;
Olliaro, Piero ;
Egan, Timothy J. .
MOLECULAR PHARMACEUTICS, 2005, 2 (03) :185-193
[7]  
DAHER WE, 2006, IN PRESS DRUG METAB
[8]   COMPARATIVE EFFICACY OF ANTIHERPES DRUGS AGAINST DIFFERENT STRAINS OF HERPES-SIMPLEX VIRUS [J].
DECLERCQ, E ;
DESCAMPS, J ;
VERHELST, G ;
WALKER, RT ;
JONES, AS ;
TORRENCE, PF ;
SHUGAR, D .
JOURNAL OF INFECTIOUS DISEASES, 1980, 141 (05) :563-574
[9]   ANTIVIRAL AND ANTIMETABOLIC ACTIVITIES OF NEPLANOCINS [J].
DECLERCQ, E .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1985, 28 (01) :84-89
[10]  
DECLERCQ E, 2006, UNPUB EXPERT REV ANT