On the medicinal chemistry of ferrocene

被引:458
作者
Fouda, Mohammad F. R. [1 ]
Abd-Elzaher, Mokhles M. [1 ]
Abdelsamaia, Rafeek A. [1 ]
Labib, Ammar A. [1 ]
机构
[1] Natl Res Ctr, Dept Inorgan Chem, Cairo, Egypt
关键词
bioorganometallic; ferrocene; anticancer; antimalarial; HIV; DNA detection; ESTROGEN-RECEPTOR MODULATORS; VITRO ANTIMALARIAL ACTIVITY; TOPOISOMERASE-II-ALPHA; ACTIVITY IN-VITRO; METALLOCENE POLYMERS; ORGANOMETALLIC ANALOG; PLASMODIUM-FALCIPARUM; BIOORGANOMETALLIC CHEMISTRY; CONFORMATIONAL-CHANGES; MOLECULAR-STRUCTURE;
D O I
10.1002/aoc.1202
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Organometallic chemistry and biochemistry have been merged in the last two decades into a new field: bioorganometallic chemistry. This new research area was devoted to the synthesis of new organometallic compounds and their biological and medical effects against some types of diseases, such as cancer and malaria. For several years, the use of ferrocene in bioorganometallic chemistry has been growing rapidly, and several promising applications have been developed since ferrocene is a stable, nontoxic compound and has good redox properties. This review will focus on ferrocenyl compounds which have been biologically evaluated against certain diseases. This area has attracted many researchers due to the promising results of some ferrocene compounds in the medicinal applications. Copyright (c) 2007 John Wiley & Sons, Ltd.
引用
收藏
页码:613 / 625
页数:13
相关论文
共 122 条
[1]  
AGNES TLC, 2006, EUR J PHARM SCI, V27, P175
[2]   Development of organometallic (organo-transition metal) pharmaceuticals [J].
Allardyce, CS ;
Dorcier, A ;
Scolaro, C ;
Dyson, PJ .
APPLIED ORGANOMETALLIC CHEMISTRY, 2005, 19 (01) :1-10
[3]   In vitro susceptibility to a new antimalarial organometallic analogue, ferroquine, of Plasmodium falciparum isolates from the Haut-Ogooue region of Gabon [J].
Atteke, C ;
Ndong, JMM ;
Aubouy, A ;
Maciejewski, L ;
Brocard, J ;
Lébibi, J ;
Deloron, P .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 2003, 51 (04) :1021-1024
[4]   Electrochemical activity of new ferrocene-labelled PNA monomers to be applied for DNA detection: Effects of the molecular structure and of the solvent [J].
Baldoli, C ;
Licandro, E ;
Maiorana, S ;
Resemini, D ;
Rigamonti, C ;
Falciola, L ;
Longhi, M ;
Mussini, PR .
JOURNAL OF ELECTROANALYTICAL CHEMISTRY, 2005, 585 (02) :197-205
[5]   Synthesis of chiral chromium tricarbonyl labeled thymine PNA monomers via the Ugi reaction [J].
Baldoli, C ;
Maiorana, S ;
Licandro, E ;
Zinzalla, G ;
Perdicchia, D .
ORGANIC LETTERS, 2002, 4 (24) :4341-4344
[6]   Synthesis and in vitro activities of ferrocenic aminohydroxynaphthoquinones against Toxoplasma gondii and Plasmodium falciparum [J].
Baramee, A ;
Coppin, A ;
Mortuaire, M ;
Pelinski, L ;
Tomavo, S ;
Brocard, J .
BIOORGANIC & MEDICINAL CHEMISTRY, 2006, 14 (05) :1294-1302
[7]   Easily synthesized antimalarial ferrocene triazacyclononane quinoline conjugates [J].
Biot, C ;
Dessolin, J ;
Ricard, I ;
Dive, D .
JOURNAL OF ORGANOMETALLIC CHEMISTRY, 2004, 689 (25) :4678-4682
[8]   Synthesis and antifungal activity of a ferrocene-fluconazole analogue [J].
Biot, C ;
François, N ;
Maciejewski, L ;
Brocard, J ;
Poulain, D .
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2000, 10 (08) :839-841
[9]  
Biot C, 1998, J LABELLED COMPD RAD, V41, P911, DOI 10.1002/(SICI)1099-1344(1998100)41:10<911::AID-JLCR145>3.0.CO
[10]  
2-4