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含3-羟基吡啶-2-羧酸的金属配合物的合成及其胰岛素模拟活性

Synthesis and insulin-mimetic activities of metal complexes with 3-hydroxypyridine-2-carboxylic acid.

作者信息

Nakai Misaki, Sekiguchi Fumi, Obata Makoto, Ohtsuki Chikara, Adachi Yusuke, Sakurai Hiromu, Orvig Chris, Rehder Dieter, Yano Shigenobu

机构信息

Division of Material Science, Graduate School of Humanities and Sciences, Nara Women's University, Kitauoyanishimachi, Nara 630-8506, Japan.

出版信息

J Inorg Biochem. 2005 Jun;99(6):1275-82. doi: 10.1016/j.jinorgbio.2005.02.026. Epub 2005 Apr 13.

Abstract

Metal complexes of 3-hydroxypyridine-2-carboxylic acid (H(2)hpic), [Co(Hhpic)(2)(H(2)O)(2)] (1), [Fe(Hhpic)(2)(H(2)O)(2)] (2), [Zn(Hhpic)(2)(H(2)O)(2)] (3), [Mn(Hhpic)(2)(H(2)O)(2)] (4), and [Cu(Hhpic)(2)] (5) have been synthesized and characterized by mass spectrometry, elemental analysis, magnetic susceptibility, infrared, electronic absorption and electron paramagnetic resonance (EPR) spectroscopies. The solid-state structure of 1 has been established by X-ray crystallography. The EPR spectra of 4 and 5 displayed six and four-line hyperfine splitting patterns, respectively, due to coupling of the unpaired electron with the (55)Mn (I=5/2) nucleus and the (63)Cu (I=3/2) nucleus. In the EPR spectrum of 5, an additional five-line super-hyperfine splitting pattern was observed at 77 K, caused by additional interaction of the unpaired electron with ligand nitrogen atoms (I=1), indicating that the structure of 5 was retained in dimethyl sulfoxide solution. The insulin-mimetic activity of these complexes was evaluated by means of in vitro measurements of the inhibition of free fatty acid (FFA) release from epinephrine-treated, isolated rat adipocytes. Complex 5 was found to exhibit the most potent insulin-mimetic activity among the complexes examined in this study.

摘要

3-羟基吡啶-2-羧酸(H₂hpic)的金属配合物,[Co(Hhpic)₂(H₂O)₂] (1)、[Fe(Hhpic)₂(H₂O)₂] (2)、[Zn(Hhpic)₂(H₂O)₂] (3)、[Mn(Hhpic)₂(H₂O)₂] (4) 和 [Cu(Hhpic)₂] (5) 已被合成,并通过质谱、元素分析、磁化率、红外、电子吸收和电子顺磁共振(EPR)光谱进行了表征。配合物1的固态结构已通过X射线晶体学确定。配合物4和5的EPR光谱分别显示出六线和四线超精细分裂模式,这是由于未成对电子与⁵⁵Mn(I = 5/2)核和⁶³Cu(I = 3/2)核的耦合所致。在配合物5的EPR光谱中,在77 K时观察到一个额外的五线超超精细分裂模式,这是由未成对电子与配体氮原子(I = 1)的额外相互作用引起的,表明配合物5的结构在二甲基亚砜溶液中得以保留。通过体外测量这些配合物对肾上腺素处理的离体大鼠脂肪细胞中游离脂肪酸(FFA)释放的抑制作用,评估了它们的胰岛素模拟活性。发现配合物5在本研究中所检测的配合物中表现出最强的胰岛素模拟活性。

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