α-酮羧酸盐与对氢在可逆交换过程中的碳-13 超极化。

IF 3.6 4区 医学 Q2 CHEMISTRY, MEDICINAL ChemMedChem Pub Date : 2024-10-04 DOI:10.1002/cmdc.202400378
Stephen J McBride, Keilian MacCulloch, Patrick TomHon, Austin Browning, Samantha Meisel, Mustapha Abdulmojeed, Boyd M Goodson, Eduard Y Chekmenev, Thomas Theis
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引用次数: 0

摘要

可逆交换信号放大(SABRE)是一种相对简单、快速的超极化技术,已被用于α-酮羧酸丙酮酸盐的超极化,丙酮酸盐是一种中心代谢产物,也是主要的超极化核磁共振成像造影剂。在这项研究中,我们发现 SABRE 可以很容易地扩展到对许多其他α-酮羧酸盐的天然丰度 13C 核进行超极化。在下列物质上观察到了超极化现象并进行了优化:R基中含有烷基链的丙酮酸盐(P13C=17%)和 2-氧代丁酸盐(P13C=25%);R基中含有羧基的草酰乙酸盐(P13C=11%)和α-酮戊二酸盐(P13C=13%);R基中含有苯基环的苯丙酮酸盐(P13C=2%)和苯基乙醛酸盐(P13C=2%)。我们观察到底物与超极化转移催化剂的新的催化活性 SABRE 结合基团,尤其是草酰乙酸。我们通过实验探索了所有这些 SABRE 系统的温度与交换率之间的联系,并建立了一个理论动力学模型,用于拟合 SABRE 活动过程中超极化的积累和衰减。
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Carbon-13 Hyperpolarization of α-Ketocarboxylates with Parahydrogen in Reversible Exchange.

Signal Amplification by Reversible Exchange (SABRE) is a relatively simple and fast hyperpolarization technique that has been used to hyperpolarize the α-ketocarboxylate pyruvate, a central metabolite and the leading hyperpolarized MRI contrast agent. In this work, we show that SABRE can readily be extended to hyperpolarize 13C nuclei at natural abundance on many other α-ketocarboxylates. Hyperpolarization is observed and optimized on pyruvate (P13C=17%) and 2-oxobutyrate (P13C=25%) with alkyl chains in the R-group, oxaloacetate (P13C=11%) and alpha-ketoglutarate (P13C=13%) with carboxylate moieties in the R group, and phenylpyruvate (P13C=2%) and phenylglyoxylate (P13C=2%) with phenyl rings in the R-group. New catalytically active SABRE binding motifs of the substrates to the hyperpolarization transfer catalyst-particularly for oxaloacetate-are observed. We experimentally explore the connection between temperature and exchange rates for all of these SABRE systems and develop a theoretical kinetic model, which is used to fit the hyperpolarization build-up and decay during SABRE activity.

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来源期刊
ChemMedChem
ChemMedChem 医学-药学
CiteScore
6.70
自引率
2.90%
发文量
280
审稿时长
1 months
期刊介绍: Quality research. Outstanding publications. With an impact factor of 3.124 (2019), ChemMedChem is a top journal for research at the interface of chemistry, biology and medicine. It is published on behalf of Chemistry Europe, an association of 16 European chemical societies. ChemMedChem publishes primary as well as critical secondary and tertiary information from authors across and for the world. Its mission is to integrate the wide and flourishing field of medicinal and pharmaceutical sciences, ranging from drug design and discovery to drug development and delivery, from molecular modeling to combinatorial chemistry, from target validation to lead generation and ADMET studies. ChemMedChem typically covers topics on small molecules, therapeutic macromolecules, peptides, peptidomimetics, and aptamers, protein-drug conjugates, nucleic acid therapies, and beginning 2017, nanomedicine, particularly 1) targeted nanodelivery, 2) theranostic nanoparticles, and 3) nanodrugs. Contents ChemMedChem publishes an attractive mixture of: Full Papers and Communications Reviews and Minireviews Patent Reviews Highlights and Concepts Book and Multimedia Reviews.
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