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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.
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页码:1849 / 1866
页数:18
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