Chemistry and biological activities of CO-releasing molecules (CORMs) and transition metal complexes

被引:171
作者
Alberto, Roger
Motterlini, Roberto
机构
[1] Univ Zurich, Inst Inorgan Chem, CH-8057 Zurich, Switzerland
[2] Norwich Pk Inst Med Res, Vasc Biol Unit, Dept Surg Res, Harrow, Middx, England
关键词
D O I
10.1039/b701992k
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
The advent of CO as a small molecule that, in addition to NO, elicits essential biological functions has initiated the search for compounds and complexes capable of releasing CO in a well defined manner under physiological conditions. Since some pharmacological and therapeutic effects of CO have been established in preclinical studies, tailor-made CO-releasing molecules (CORMs) which could be utilized as pharmaceuticals could be of great benefit for many patients. Release of CO2 is one of the most common features in chemistry and NO producing molecules are very well established but compounds with CO-releasing properties are rare. Some of the more promising candidates and molecules under study are discussed in this article. Furthermore, molecules that possess intrinsic features to serve as potential CO-RMs and merit indepth investigations are proposed. The focus is thereby on main group compounds and on transition element complexes. It should be emphasized that CORMs not only have encouraging prospects as therapeutic agents but may also be signficant for synthetic pathways to novel complexes containing the CO ligand. To underline the prospects of CORMs, the chemical part is embedded in a biological and medicinal context.
引用
收藏
页码:1651 / 1660
页数:10
相关论文
共 103 条
[1]   RADIOLYSIS AND PHOTOLYSIS OF AQUEOUS FORMIC ACID - CARBON MONOXIDE FORMATION [J].
ADAMS, GE ;
HART, EJ .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1962, 84 (21) :3994-&
[2]  
Aebischer N, 2000, ANGEW CHEM INT EDIT, V39, P254, DOI 10.1002/(SICI)1521-3773(20000103)39:1<254::AID-ANIE254>3.0.CO
[3]  
2-F
[4]   Heme oxygenase-1-derived carbon monoxide protects hearts from transplant-associated ischemia reperfusion injury [J].
Akamatsu, Y ;
Haga, M ;
Tyagi, S ;
Yamashita, K ;
Graça-Souza, AV ;
Ollinger, R ;
Czismadia, E ;
May, GA ;
Ifedigbo, E ;
Otterbein, LE ;
Bach, FH ;
Soares, MP .
FASEB JOURNAL, 2004, 18 (02) :771-+
[5]   Steps towards [(C5Me5)TcO3]:: Novel synthesis of [(C5Me5)Tc(CO)3] from [{Tc(μ3-OH)(CO)3}4] and oxidation of [(C5Me5)M(CO)3] (M = Tc, Re) with Br2 [J].
Alberto, R ;
Schibli, R ;
Egli, A ;
Abram, U ;
Abram, S ;
Kaden, TA ;
Schubiger, PA .
POLYHEDRON, 1998, 17 (07) :1133-1140
[6]   Synthesis and properties of boranocarbonate:: A convenient in situ CO source for the aqueous preparation of [99mTC(OH2)3(CO)3]+ [J].
Alberto, R ;
Ortner, K ;
Wheatley, N ;
Schibli, R ;
Schubiger, AP .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2001, 123 (13) :3135-3136
[7]  
ALBERTO RA, 2001, Patent No. 2001025243
[8]   Increase in exhaled carbon monoxide during exacerbations of cystic fibrosis [J].
Antuni, JD ;
Kharitonov, SA ;
Hughes, D ;
Hodson, ME ;
Barnes, PJ .
THORAX, 2000, 55 (02) :138-142
[9]   Modulation of thrombin-induced neuroinflammation in BV-2 microglia by carbon monoxide-releasing molecule 3 [J].
Bani-Hani, Mohamed G. ;
Greenstein, David ;
Mann, Brian E. ;
Green, Colin J. ;
Motterlini, Roberto .
JOURNAL OF PHARMACOLOGY AND EXPERIMENTAL THERAPEUTICS, 2006, 318 (03) :1315-1322
[10]   Synthesis of amine-dicyanohydroboranes, [amine-bis(ethylnitrilium)hydroboron(2+)] tetrafluoroborates, and their derivatives as precursors of amine-dicarboxyboranes [J].
Berente, Z ;
Györi, B .
INORGANIC CHEMISTRY, 1999, 38 (23) :5250-5256