The [(Cp)M(CO)3] (M=Re, 99mTc) Building Block for Imaging Agents and Bioinorganic Probes: Perspectives and Limitations

被引:26
|
作者
Can, Daniel [1 ]
N'Dongo, Harmel W. Peindy [1 ]
Spingler, Bernhard [1 ]
Schmutz, Paul [1 ]
Raposinho, Paula [2 ]
Santos, Isabel [2 ]
Alberto, Roger [1 ]
机构
[1] Univ Zurich, Inst Organ Chem, CH-8057 Zurich, Switzerland
[2] Univ Tecn Lisbao, IST ITN, Inst Super Tecn, P-2686953 Sacavem, Portugal
关键词
Diels?Alder reaction; Technetium complexes; Rhenium complexes; Histone deacetylase (HDAC); Inhibitors; X-Ray crystallography; HISTONE DEACETYLASE INHIBITORS; PROTEIN-KINASE INHIBITORS; BIOLOGICAL EVALUATION; METAL-COMPLEXES; BIOORGANOMETALLIC CHEMISTRY; BIOMEDICAL APPLICATIONS; MYOCARDIAL-METABOLISM; LIGAND COMPLEXES; CHEMICAL SPACE; TECHNETIUM;
D O I
10.1002/cbdv.201200076
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
Starting from asymmetric Thiele's acid derivatives, two different imaging probes [99mTc(CO)3(CpR)] (R=potential targeting vector) are generated simultaneously in one-pot and from one substrate. This extends the previously introduced labeling strategy of metal-mediated retro-Diels?Alder reaction with HCp-R dimers. We demonstrate that chemically active functionalities such as hydroxamic acids are not following this labeling strategy. Adopting the principle of replacing phenyl rings by [Re(CO)3(Cp)] entities, potent histone deacetylase (HDAC)-inhibiting Re analogs of suberoylanlilide hydroxamic acid (SAHA; N-hydroxy-N'-phenyloctanediamide) were synthesized and characterized. Cytotoxic evaluation on different tumor cell lines revealed low IC50 values [mu M] for these compounds, comparable to their purely organic congeners.
引用
收藏
页码:1849 / 1866
页数:18
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