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通过微波辅助 Atwal 反应获得的 6-二茂铁/杂环-2-氨基嘧啶和 5-二茂铁-1H-吡唑衍生物的合成、对接、机器学习和抗增殖活性作为潜在的抗癌剂。

Synthesis, docking, machine learning and antiproliferative activity of the 6-ferrocene/heterocycle-2-aminopyrimidine and 5-ferrocene-1H-Pyrazole derivatives obtained by microwave-assisted Atwal reaction as potential anticancer agents.

机构信息

Chemistry Department, Federal University of Espírito Santo, Vitória, Espírito Santo CEP.:29075-910, Brazil.

Physical Department, Minas Gerais Federal University, Av. Antônio Carlos 6627, Pampulha, Belo Horizonte, Minas Gerais CEP.: 30161-970 Brazil.

出版信息

Bioorg Med Chem Lett. 2021 Sep 15;48:128240. doi: 10.1016/j.bmcl.2021.128240. Epub 2021 Jul 2.

DOI:10.1016/j.bmcl.2021.128240
PMID:34217828
Abstract

A simple and fast methodology under microwave irradiation for the synthesis of 2-aminopyrimidine and pyrazole derivatives using Atwal reaction is reported. After the optimization of the reaction conditions, eight 2-aminolpyrimidines containing ferrocene and heterocycles and three ferrocene pyrazoles were synthesized from the respective chalcones in good yields. Eight compounds had their structure determined by X-ray diffraction. The molecular hybrid 6a-h and 9a-c were tested on four cancer cell lines - HCT116, PC3, HL60 and SNB19 - where four pyrimidine 6a, 6f-h and one pyrazole 9c derivatives show promising antiproliferative activity. In addition, docking simulation and machine learning methods were carried out to explain the biological activity achieved by the synthetized compounds.

摘要

本文报道了一种在微波辐射下通过 Atwal 反应合成 2-氨基嘧啶和吡唑衍生物的简单、快速方法。在优化反应条件后,从相应的查尔酮出发,合成了 8 个含有二茂铁和杂环的 2-氨基嘧啶和 3 个二茂铁吡唑,产率良好。其中 8 个化合物的结构通过 X 射线衍射确定。对四个癌细胞系 HCT116、PC3、HL60 和 SNB19 进行了分子杂交 6a-h 和 9a-c 的测试,其中嘧啶 6a、6f-h 的四个衍生物和吡唑 9c 的一个衍生物表现出有希望的抗增殖活性。此外,还进行了对接模拟和机器学习方法,以解释所合成化合物的生物活性。

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