Advances in iron chelation: an update

被引:75
作者
Heli, Hossein [2 ]
Mirtorabi, Siamak [3 ]
Karimian, Khashayar [1 ]
机构
[1] Arasto Pharmaceut Chem Inc, Tehran 1438933743, Iran
[2] Islamic Azad Univ, Sci & Res Branch, Dept Chem, Fars 7348113111, Iran
[3] Avicenna Labs Inc, Tehran 1438933743, Iran
关键词
AIDS; asthma; cancer; cardiotoxicity; fibrosis; infection; iron chelation; malaria; neurodegenerative disease; ototoxicity; reactive oxygen species; sideromycine; thalassemia; TRANSFUSION-DEPENDENT THALASSEMIA; CHRONIC ANTHRACYCLINE CARDIOTOXICITY; PYRIDOXAL ISONICOTINOYL HYDRAZONE; DRUG-DELIVERY AGENTS; INDUCIBLE FACTOR FIH; LONG-TERM THERAPY; BETA-THALASSEMIA; RIBONUCLEOTIDE REDUCTASE; OXIDATIVE STRESS; CELL-GROWTH;
D O I
10.1517/13543776.2011.569493
中图分类号
R914 [药物化学];
学科分类号
100705 [微生物与生化药学];
摘要
Introduction: Oxidative stress (caused by excess iron) can result in tissue damage, organ failure and finally death, unless treated by iron chelators. The causative factor in the etiology of a variety of disease states is the presence of iron-generated reactive oxygen species (ROS), which can result in cell damage or which can affect the signaling pathways involved in cell necrosis-apoptosis or organ fibrosis, cancer, neurodegeneration and cardiovascular, hepatic or renal dysfunctions. Iron chelators can reduce oxidative stress by the removal of iron from target tissues. Equally as important, removal of iron from the active site of enzymes that play key roles in various diseases can be of considerable benefit to the patients. Areas covered: This review focuses on iron chelators used as therapeutic agents. The importance of iron in oxidative damage is discussed, along with the three clinically approved iron chelators. Expert opinion: A number of iron chelators are used as approved therapeutic agents in the treatment of thalassemia major, asthma, fungal infections and cancer. However, as our knowledge about the biochemistry of iron and its role in etiologies of seemingly unrelated diseases increases, new applications of the approved iron chelators, as well as the development of new iron chelators, present challenging opportunities in the areas of drug discovery and development.
引用
收藏
页码:819 / 856
页数:38
相关论文
共 486 条
[41]
3,5-disubstituted-4-hydroxyphenyls linked to 3-hydroxy-2-methyl-4(1H)-pyridinone:: Potent inhibitors of lipid peroxidation and cell toxicity [J].
Bebbington, D ;
Monck, NJT ;
Gaur, S ;
Palmer, AM ;
Benwell, K ;
Harvey, V ;
Malcolm, CS ;
Porter, RHP .
JOURNAL OF MEDICINAL CHEMISTRY, 2000, 43 (15) :2779-2782
[42]
Ben-Shachar D., 2005, U. S. Patent, Patent No. [6,855,711, 6855711]
[43]
Comparison of Clinically Used and Experimental Iron Chelators for Protection against Oxidative Stress-Induced Cellular Injury [J].
Bendova, Petra ;
Mackova, Eliska ;
Haskova, Pavlina ;
Vavrova, Anna ;
Jirkovsky, Eduard ;
Sterba, Martin ;
Popelova, Olga ;
Kalinowski, Danuta S. ;
Kovarikova, Petra ;
Vavrova, Katerina ;
Richardson, Des R. ;
Simunek, Tomas .
CHEMICAL RESEARCH IN TOXICOLOGY, 2010, 23 (06) :1105-1114
[44]
Zileuton: clinical implications of 5-Lipoxygenase inhibition in severe airway disease [J].
Berger, W. ;
De Chandt, M. T. M. ;
Cairns, C. B. .
INTERNATIONAL JOURNAL OF CLINICAL PRACTICE, 2007, 61 (04) :663-676
[45]
BERGERON, 2007, Patent No. 20070232664
[46]
BERGERON, 2005, Patent No. 20050245579
[47]
Design, synthesis, and testing of non-nephrotoxic desazadesferrithiocin polyether analogues [J].
Bergeron, Raymond J. ;
Wiegand, Jan ;
McManis, James S. ;
Bharti, Neelam ;
Singh, Shailendra .
JOURNAL OF MEDICINAL CHEMISTRY, 2008, 51 (13) :3913-3923
[48]
IRON - A CONTROLLING NUTRIENT IN PROLIFERATIVE PROCESSES [J].
BERGERON, RJ .
TRENDS IN BIOCHEMICAL SCIENCES, 1986, 11 (03) :133-136
[49]
Desketoneoenactin-siderophore conjugates for Candida :: Evidence of iron transport-dependent species selectivity [J].
Bernier, G ;
Girijavallabhan, V ;
Murray, A ;
Niyaz, N ;
Ding, PY ;
Miller, MJ ;
Malouin, F .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2005, 49 (01) :241-248
[50]
Bezkorovainy A., 1980, Biochemistry of Nonheme Iron, P343