New trends in anti-malarial agents

被引:57
作者
Frédérich, M
Dogné, JM
Angenot, L
De Mol, P
机构
[1] Univ Liege, CHU Sart Tilman B36, Nat & Synth Drugs Res Ctr, Lab Pharmacognosy, B-4000 Liege, Belgium
[2] Univ Liege, CHU Sart Tilman B23, Lab Med Microbiol, B-4000 Liege, Belgium
[3] Univ Liege, CHU Sart Tilman B36, Nat & Synth Drugs Res Ctr, Med Chem Lab, B-4000 Liege, Belgium
关键词
D O I
10.2174/0929867023369691
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Malaria is the major parasitic infection in many tropical and subtropical regions, leading to more than one million deaths (principally young African children) out of 400 million cases each year (WHO world health report 2000). More than half of the world's population live in areas where they remain at risk of malaria infection. During last years, the situation has worsened in many ways, mainly due to malarial parasites becoming increasingly resistant to several antimalarial drugs. Furthermore, the control of malaria is becoming more complicated by the parallel spread of resistance of the mosquito vector to currently available insecticides. Discovering new drugs in this field is therefore a health priority. Several new molecules are under investigation. This review describes the classical treatments of malaria and the latest discoveries in antimalarial agents, especially artemisinin and its recent derivatives as well as the novel peroxidic compounds.
引用
收藏
页码:1435 / 1456
页数:22
相关论文
共 138 条
[51]   SYNTHESIS AND ANTIMALARIAL ACTIVITY OF (+)-DEOXOARTEMISININ [J].
JUNG, M ;
LI, X ;
BUSTOS, DA ;
ELSOHLY, HN ;
MCCHESNEY, JD ;
MILHOUS, WK .
JOURNAL OF MEDICINAL CHEMISTRY, 1990, 33 (05) :1516-1518
[52]   Malaria chemoprophylaxis in the age of drug resistance. I. Currently recommended drug regimens [J].
Kain, KC ;
Shanks, GD ;
Keystone, JS .
CLINICAL INFECTIOUS DISEASES, 2001, 33 (02) :226-234
[53]   Ferryl-oxo heme intermediate in the antimalarial mode of action of artemisinin [J].
Kapetanaki, S ;
Varotsis, C .
FEBS LETTERS, 2000, 474 (2-3) :238-241
[54]   MICROBIAL AND MAMMALIAN METABOLISM STUDIES ON THE SEMISYNTHETIC ANTIMALARIAL, DEOXOARTEMISININ [J].
KHALIFA, SI ;
BAKER, JK ;
JUNG, M ;
MCCHESNEY, JD ;
HUFFORD, CD .
PHARMACEUTICAL RESEARCH, 1995, 12 (10) :1493-1498
[55]   MITOCHONDRIA AS THE SITE OF ACTION OF TETRACYCLINE ON PLASMODIUM-FALCIPARUM [J].
KIATFUENGFOO, R ;
SUTHIPHONGCHAI, T ;
PRAPUNWATTANA, P ;
YUTHAVONG, Y .
MOLECULAR AND BIOCHEMICAL PARASITOLOGY, 1989, 34 (02) :109-115
[56]   Membrane transport in the malaria-infected erythrocyte [J].
Kirk, K .
PHYSIOLOGICAL REVIEWS, 2001, 81 (02) :495-537
[57]   Transport proteins of Plasmodium falciparum:: defining the limits of metabolism [J].
Krishna, S ;
Webb, R ;
Woodrow, C .
INTERNATIONAL JOURNAL FOR PARASITOLOGY, 2001, 31 (12) :1331-1342
[58]   ENERGY-DEPENDENCE OF CHLOROQUINE ACCUMULATION AND CHLOROQUINE EFFLUX IN PLASMODIUM-FALCIPARUM [J].
KROGSTAD, DJ ;
GLUZMAN, IY ;
HERWALDT, BL ;
SCHLESINGER, PH ;
WELLEMS, TE .
BIOCHEMICAL PHARMACOLOGY, 1992, 43 (01) :57-62
[59]   DEMONSTRATION OF HYPNOZOITES IN SPOROZOITE-TRANSMITTED PLASMODIUM-VIVAX INFECTION [J].
KROTOSKI, WA ;
COLLINS, WE ;
BRAY, RS ;
GARNHAM, PCC ;
COGSWELL, FB ;
GWADZ, RW ;
KILLICKKENDRICK, R ;
WOLF, R ;
SINDEN, R ;
KOONTZ, LC ;
STANFILL, PS .
AMERICAN JOURNAL OF TROPICAL MEDICINE AND HYGIENE, 1982, 31 (06) :1291-1293
[60]   THE ANTIMALARIAL ACTION ON PLASMODIUM-FALCIPARUM OF QINGHAOSU AND ARTESUNATE IN COMBINATION WITH AGENTS WHICH MODULATE OXIDANT STRESS [J].
KRUNGKRAI, SR ;
YUTHAVONG, Y .
TRANSACTIONS OF THE ROYAL SOCIETY OF TROPICAL MEDICINE AND HYGIENE, 1987, 81 (05) :710-714