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通过无金属光催化方法进行的创新型树脂上和溶液中肽模拟物合成。

Innovative On-Resin and in Solution Peptidomimetics Synthesis via Metal-Free Photocatalytic Approach.

作者信息

Gandini Tommaso, Vaghi Francesco, Laface Zoe, Macetti Giovanni, Bossi Alberto, Penconi Marta, Luisa Gelmi Maria, Bucci Raffaella

机构信息

Dipartimento di Scienze Farmaceutiche, Sez. Chimica Generale e Organica A. Marchesini, Università degli Studi di Milano, Via Venezian 21, 20133, Milan, Italy.

Dipartimento di Scienze Chimiche, Università degli Studi di Padova, Via Marzolo 1, 35131, Padova, Italy.

出版信息

Chemistry. 2024 Dec 5;30(68):e202402790. doi: 10.1002/chem.202402790. Epub 2024 Nov 8.

Abstract

Nowadays, peptidomimetics are widely studied, being useful tools in drug discovery and medicinal chemistry. The coupling between a carboxylic acid with an amine to form a peptide bond is the most common reaction to obtain peptides/peptidomimetics. In this work, we have investigated an innovative metal-free photoredox-catalyzed carbamoylation to form peptidomimetics thanks to the reaction between dihydropyridines functionalized with amino acids (or peptide sequences) and differently functionalized imines. As the organic photocatalyst, we used 4CzIPN, a donor-acceptor cyanoarene vastly used in photoredox catalysis. By easily modulating the amino acid (or peptide sequence), which is directly attached to the dihydropyridine, we proposed this key-reaction as new valuable method to obtain peptidomimetics, in situ building the not-natural portion of the sequence. Moreover, we successfully employed this methodology in solid phase peptide synthesis, both inserting the new photoredox-generated amino acid at the end or in the middle of the sequence. Peptides with different lengths and secondary structures were prepared, proving the success of this approach, even in sterically hindered environment. Herein, to the best of our knowledge, we describe the first photocatalytic protocol which allows the building of the peptide backbone, with the possibility of simultaneously inserting a non-coded amino acid in the sequence.

摘要

如今,拟肽受到广泛研究,是药物发现和药物化学中的有用工具。羧酸与胺之间形成肽键的偶联反应是获得肽/拟肽的最常见反应。在这项工作中,我们研究了一种创新的无金属光氧化还原催化氨甲酰化反应,通过用氨基酸(或肽序列)功能化的二氢吡啶与不同功能化的亚胺之间的反应来形成拟肽。作为有机光催化剂,我们使用了4CzIPN,一种在光氧化还原催化中广泛使用的供体-受体氰基芳烃。通过轻松调节直接连接到二氢吡啶上的氨基酸(或肽序列),我们提出这种关键反应是获得拟肽的一种新的有价值方法,可原位构建序列中的非天然部分。此外,我们成功地将这种方法应用于固相肽合成,既可以在序列末端也可以在序列中间插入新的光氧化还原产生的氨基酸。制备了具有不同长度和二级结构的肽,证明了这种方法的成功,即使在空间位阻环境中也是如此。在此,据我们所知,我们描述了第一个光催化方案,该方案允许构建肽主链,并有可能在序列中同时插入一个非编码氨基酸。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0284/11618039/f81bc7d30be3/CHEM-30-e202402790-g004.jpg

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