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新型高效超氧阴离子歧化催化剂。锰(III)邻甲氧基乙基吡啶基和二邻甲氧基乙基咪唑基卟啉。

New class of potent catalysts of O2.-dismutation. Mn(III) ortho-methoxyethylpyridyl- and di-ortho-methoxyethylimidazolylporphyrins.

作者信息

Batinić-Haberle Ines, Spasojević Ivan, Stevens Robert D, Hambright Peter, Neta Pedatsur, Okado-Matsumoto Ayako, Fridovich Irwin

机构信息

Department of Radiation Oncology, Duke University Medical Center, Durham, NC 27710, USA.

出版信息

Dalton Trans. 2004 Jun 7(11):1696-702. doi: 10.1039/b400818a. Epub 2004 May 5.

Abstract

Three new Mn(III) porphyrin catalysts of O2.-dismutation (superoxide dismutase mimics), bearing ether oxygen atoms within their side chains, were synthesized and characterized: Mn(III) 5,10,15,20-tetrakis[N-(2-methoxyethyl)pyridinium-2-yl]porphyrin (MnTMOE-2-PyP(5+)), Mn(III)5,10,15,20-tetrakis[N-methyl-N'-(2-methoxyethyl)imidazolium-2-yl]porphyrin (MnTM,MOE-2-ImP(5+)) and Mn(III) 5,10,15,20-tetrakis[N,N'-di(2-methoxyethyl)imidazolium-2-yl]porphyrin (MnTDMOE-2-ImP(5+)). Their catalytic rate constants for O2.-dismutation (disproportionation) and the related metal-centered redox potentials vs. NHE are: log k(cat)= 8.04 (E(1/2)=+251 mV) for MnTMOE-2-PyP(5+), log k(cat)= 7.98 (E(1/2)=+356 mV) for MnTM,MOE-2-ImP(5+) and log k(cat)= 7.59 (E(1/2)=+365 mV) for MnTDMOE-2-ImP(5+). The new porphyrins were compared to the previously described SOD mimics Mn(III) 5,10,15,20-tetrakis(N-ethylpyridinium-2-yl)porphyrin (MnTE-2-PyP(5+)), Mn(III) 5,10,15,20-tetrakis(N-n-butylpyridinium-2-yl)porphyrin (MnTnBu-2-PyP(5+)) and Mn(III) 5,10,15,20-tetrakis(N,N'-diethylimidazolium-2-yl)porphyrin (MnTDE-2-ImP(5+)). MnTMOE-2-PyP(5+) has side chains of the same length and the same E(1/2), as MnTnBu-2-PyP(5+)(k(cat)= 7.25, E(1/2)=+ 254 mV), yet it is 6-fold more potent a catalyst of O2.-dismutation , presumably due to the presence of the ether oxygen. The log k(cat)vs. E(1/2) relationship for all Mn porphyrin-based SOD mimics thus far studied is discussed. None of the new compounds were toxic to Escherichia coli in the concentration range studied (up to 30 microM), and protected SOD-deficient E. coli in a concentration-dependent manner. At 3 microM levels, the MnTDMOE-2-ImP(5+), bearing an oxygen atom within each of the eight side chains, was the most effective and offered much higher protection than MnTE-2-PyP(5+), while MnTDE-2-ImP(5+) was of very low efficacy.

摘要

合成并表征了三种新型的具有超氧阴离子歧化活性(超氧化物歧化酶模拟物)的含醚氧原子侧链的锰(III)卟啉催化剂:锰(III)5,10,15,20-四(N-(2-甲氧基乙基)吡啶鎓-2-基)卟啉(MnTMOE-2-PyP(5+))、锰(III)5,10,15,20-四(N-甲基-N'-(2-甲氧基乙基)咪唑鎓-2-基)卟啉(MnTM,MOE-2-ImP(5+))和锰(III)5,10,15,20-四(N,N'-二(2-甲氧基乙基)咪唑鎓-2-基)卟啉(MnTDMOE-2-ImP(5+))。它们的超氧阴离子歧化(歧化反应)催化速率常数以及相对于标准氢电极(NHE)的相关金属中心氧化还原电位分别为:MnTMOE-2-PyP(5+)的log k(cat)= 8.04(E(1/2)= +251 mV),MnTM,MOE-2-ImP(5+)的log k(cat)= 7.98(E(1/2)= +356 mV),MnTDMOE-2-ImP(5+)的log k(cat)= 7.59(E(1/2)= +365 mV)。将这些新型卟啉与先前描述的超氧化物歧化酶模拟物锰(III)5,10,15,20-四(N-乙基吡啶鎓-2-基)卟啉(MnTE-2-PyP(5+))、锰(III)5,10,15,20-四(N-正丁基吡啶鎓-2-基)卟啉(MnTnBu-2-PyP(5+))和锰(III)5,10,15,20-四(N,N'-二乙基咪唑鎓-2-基)卟啉(MnTDE-2-ImP(5+))进行了比较。MnTMOE-2-PyP(5+)与MnTnBu-2-PyP(5+)(k(cat)= 7.25,E(1/2)= +254 mV)具有相同长度的侧链和相同的E(1/2),但其超氧阴离子歧化催化活性却是后者的6倍,推测这是由于醚氧的存在。讨论了迄今为止所研究的所有基于锰卟啉的超氧化物歧化酶模拟物的log k(cat)与E(1/2)的关系。在所研究的浓度范围(高达30 microM)内,这些新化合物对大肠杆菌均无毒性,并以浓度依赖的方式保护超氧化物歧化酶缺陷型大肠杆菌。在3 microM水平时,每个八个侧链中都含有一个氧原子的MnTDMOE-2-ImP(5+)最为有效,其提供的保护比MnTE-2-PyP(5+)高得多,而MnTDE-2-ImP(5+)的效果则非常低。

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