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首页> 外文期刊>Bioconjugate Chemistry >Synthesis of nonluminescent lanthanide(III) chelates tethered to an aminooxy group and their applicability to biomolecule derivatization
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Synthesis of nonluminescent lanthanide(III) chelates tethered to an aminooxy group and their applicability to biomolecule derivatization

机译:束缚在氨氧基上的不发光镧系元素螯合物的合成及其在生物分子衍生化中的应用

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摘要

Synthesis of nonluminescent lanthanide(III) chelates tethered to an aminooxy group (i.e., 1-[4-(6-aminooxyhexamido)benzyl]diethylenetriaminetetraacetic acid lanthanides(III), 6a-d, where Ln~(3+) is Eu, Dy, Sm, and Tb) is described. Their applicability to biomolecule derivatization is demonstrated by allowing them to react with a synthetic oligopeptide, a protein, two synthetic drugs, and a steroid. The oligopeptide and protein were linked to 6 after preoxidation of their N-terminal serine residues, while the drugs and the steroid reacted via their ketone functionality. Also some application data is included.
机译:拴系在氨基氧基上的不发光镧系元素(III)螯合物的合成(即1- [4-(6-氨基氧基六亚氨基)苄基]二亚乙基三胺四乙酸镧系元素(III),6a-d,其中Ln〜(3+)为Eu,Dy (Sm和Tb)。通过使它们与合成的寡肽,蛋白质,两种合成药物和类固醇反应,证明了它们对生物分子衍生化的适用性。寡肽和蛋白质的N端丝氨酸残基预氧化后与6连接,而药物和类固醇通过其酮官能团反应。还包括一些应用程序数据。

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