Biological Actions of Artemisinin: Insights from Medicinal Chemistry Studies

被引:90
作者
Li, Jian [1 ]
Zhou, Bing [1 ]
机构
[1] Tsinghua Univ, State Key Lab Biomembrane & Membrane Biotechnol, Sch Life Sci, Beijing 100084, Peoples R China
关键词
artemisinin; PfATP6; heme; iron; mitochondria; FALCIPARUM MALARIA PARASITES; CHLOROQUINE-RESISTANT PARASITES; ANTIMALARIAL AGENT ARTEMISININ; CONTROLLED TUMOR PROTEIN; PLASMODIUM-FALCIPARUM; IN-VITRO; RODENT MALARIA; ENDOPEROXIDE ANTIMALARIAL; SYNTHETIC 1,2,4-TRIOXANES; MOLECULAR DOCKING;
D O I
10.3390/molecules15031378
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
Artemisinins have become essential antimalarial drugs for increasingly widespread drug-resistant malaria strains. Although tremendous efforts have been devoted to decipher how this class of molecules works, their exact antimalarial mechanism is still an enigma. Several hypotheses have been proposed to explain their actions, including alkylation of heme by carbon-centered free radicals, interference with proteins such as the sarcoplasmic/endoplasmic calcium ATPase (SERCA), as well as damaging of normal mitochondrial functions. Besides artemisinins, other endoperoxides with various backbones have also been synthesized, some of which showed comparable or even higher antimalarial effects. It is noteworthy that among these artemisinin derivatives, some enantiomers displayed similar in vitro malaria killing efficacy. In this article, the proposed mechanisms of action of artemisinins are reviewed in light of medicinal chemistry findings characterized by efficacy-structure studies, with the hope of gaining more insight into how these potent drugs work.
引用
收藏
页码:1378 / 1397
页数:20
相关论文
共 113 条
[31]  
HUANG Q, 2008, J TSINGHUA U SCI TEC, V43, P408
[33]   Resistance of Plasmodium falciparum field isolates to in-vitro artemether and point mutations of the SERCA-type PfATPase6 [J].
Jambou, R ;
Legrand, E ;
Niang, M ;
Khim, N ;
Lim, P ;
Volney, B ;
Ekala, MT ;
Bouchier, C ;
Esterre, P ;
Fandeur, T ;
Mercereau-Puijalon, O .
LANCET, 2005, 366 (9501) :1960-1963
[34]   New developments in synthetic peroxidic drugs as artemisinin mimics [J].
Jefford, Charles W. .
DRUG DISCOVERY TODAY, 2007, 12 (11-12) :487-495
[35]   SYNTHESIS, STRUCTURE, AND ANTIMALARIAL ACTIVITY OF TRICYCLIC 1,2,4-TRIOXANES RELATED TO ARTEMISININ [J].
JEFFORD, CW ;
VELARDE, JA ;
BERNARDINELLI, G ;
BRAY, DH ;
WARHURST, DC ;
MILHOUS, WK .
HELVETICA CHIMICA ACTA, 1993, 76 (08) :2775-2788
[36]   SYNTHESIS, STRUCTURE, AND ANTIMALARIAL ACTIVITY OF SOME ENANTIOMERICALLY PURE, CIS-FUSED CYCLOPENTENO-1,2,4-TRIOXANES [J].
JEFFORD, CW ;
KOHMOTO, S ;
JAGGI, D ;
TIMARI, G ;
ROSSIER, JC ;
RUDAZ, M ;
BARBUZZI, O ;
GERARD, D ;
BURGER, U ;
KAMALAPRIJA, P ;
MAREDA, J ;
BERNARDINELLI, G ;
MANZANARES, I ;
CANFIELD, CJ ;
FLECK, SL ;
ROBINSON, BL ;
PETERS, W .
HELVETICA CHIMICA ACTA, 1995, 78 (03) :647-662
[37]   SYNTHESIS OF NEW 1,2,4-TRIOXANES AND THEIR ANTIMALARIAL ACTIVITY [J].
JEFFORD, CW ;
MCGORAN, EC ;
BOUKOUVALAS, J ;
RICHARDSON, G ;
ROBINSON, BL ;
PETERS, W .
HELVETICA CHIMICA ACTA, 1988, 71 (07) :1805-1812
[38]   QINGHAOSU-INDUCED CHANGES IN THE MORPHOLOGY OF PLASMODIUM-INUI [J].
JIANG, JB ;
JACOBS, G ;
LIANG, DS ;
AIKAWA, M .
AMERICAN JOURNAL OF TROPICAL MEDICINE AND HYGIENE, 1985, 34 (03) :424-428
[39]   In vitro inhibition of Toxoplasma gondii by four new derivatives of artemisinin [J].
Jones-Brando, Lorraine ;
D'Angelo, John ;
Posner, Gary H. ;
Yolken, Robert .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2006, 50 (12) :4206-4208
[40]   OPIATES SUPPRESS CARRAGEENAN-INDUCED EDEMA AND HYPERTHERMIA AT DOSES THAT INHIBIT HYPERALGESIA [J].
JORIS, J ;
COSTELLO, A ;
DUBNER, R ;
HARGREAVES, KM .
PAIN, 1990, 43 (01) :95-103