Iron Dienylphosphate Tricarbonyl Complexes as Water-Soluble Enzyme-Triggered CO-Releasing Molecules (ET-CORMs)

被引:60
|
作者
Romanski, Steffen [1 ]
Ruecker, Hannelore [2 ]
Stamellou, Eleni [3 ]
Guttentag, Miguel [4 ]
Neudoerfl, Joerg-Martin [1 ]
Alberto, Roger [4 ]
Amslinger, Sabine [2 ]
Yard, Benito [3 ]
Schmalz, Hans-Guenther [1 ]
机构
[1] Univ Cologne, Dept Chem, D-50939 Cologne, Germany
[2] Univ Regensburg, Inst Organ Chem, D-93503 Regensburg, Germany
[3] Univ Med Mannheim, Med Klin, D-68167 Mannheim, Germany
[4] Univ Zurich, Inst Anorgan Chem, CH-8057 Zurich, Switzerland
关键词
CARBON-MONOXIDE RELEASE; THERAPEUTIC APPLICATIONS; COORDINATION; EXAMPLE;
D O I
10.1021/om300359a
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
A series of racemic phosphoryloxy-substituted (eta(4)-cyclohexadiene)Fe(CO)(3) complexes was synthesized by exploiting the O-phosphorylation of (dienol)Fe(CO)(3) intermediates generated in situ from the corresponding triisopropylsiloxy-protected complexes. The phosphorylated products were fully characterized by spectroscopic methods, including single-crystal X-ray diffraction in four cases. Monodeprotection of two dimethyl phosphate derivatives with trimethylamine led to the tetramethylammonium salts of the (cyclohexadienyl methyl phosphate)Fe(CO)(3) complexes. These compounds are the first water-soluble enzyme-trigged CO-releasing molecules (ET-CORMs). The phosphatase-induced CO release was monitored by means of GC. The biological activity was assessed in different cellular assays. The compounds were shown to be only slightly toxic, and a moderate anti-inflammatory potential was determined in an assay based on the inhibition of inducible NO synthase (iNOS)-induced NO production.
引用
收藏
页码:5800 / 5809
页数:10
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