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含氨基酸有机阳离子的 Keggin 型多金属氧酸盐的合成及抗 HIV-1 活性评价。

Synthesis and anti-HIV-1 activity evaluation of Keggin-type polyoxometalates with amino acid as organic cations.

机构信息

Beijing Tide Pharmaceutical Co., Ltd, Beijing 100176, China.

Faculty of Environment and Life, Beijing University of Technology, Beijing 100124, China.

出版信息

Bioorg Med Chem Lett. 2023 Jul 15;91:129380. doi: 10.1016/j.bmcl.2023.129380. Epub 2023 Jun 16.

Abstract

Polyoxometalates (POMs), as a class of multinuclear metal oxygen clusters, have promising biological activities. And their amino acid derivatives will lead to better pharmacological activity by the diversity in structures and properties. With reference to the anti-HIV-1 activities of PM-19 (KPTiWO) and its pyridinium derivatives, a series of novel Keggin-type POMs with amino acid as organic cations (APTiWO) were synthesized by hydrothermal synthetic method. The final products were characterized by H NMR, Elemental analyzes and single crystal X-ray diffraction. All the synthesized compounds were obtained in the yields of 44.3-61.7% and evaluated the cytotoxicity and anti-HIV-1 activity in vitro. Compared with the reference compound PM-19, the target compounds had a lower toxicity to TZM-bl cells and a higher inhibitory activity against HIV-1. Among them, compound A3 showed higher anti-HIV-1 activity with IC of 0.11 nM than that of PM-19 with 4.68 nM. This study demonstrated that combination of Keggin-type POMs and amino acids can be a new strategy to enhance the anti-HIV-1 biological activity of POMs. All results will be expected to helpful for developing more potent and effective HIV-1 inhibitors.

摘要

多金属氧酸盐(POMs)作为一类多核金属氧簇,具有有前途的生物活性。它们的氨基酸衍生物通过结构和性质的多样性将导致更好的药理活性。参考 PM-19(KPTiWO)及其吡啶𬭩衍生物的抗 HIV-1 活性,通过水热合成方法合成了一系列具有氨基酸作为有机阳离子(APTiWO)的新型 Keggin 型 POM。最终产物通过 1 H NMR、元素分析和单晶 X 射线衍射进行了表征。所有合成的化合物的产率为 44.3-61.7%,并在体外评估了细胞毒性和抗 HIV-1 活性。与参考化合物 PM-19 相比,目标化合物对 TZM-bl 细胞的毒性更低,对 HIV-1 的抑制活性更高。其中,化合物 A3 的抗 HIV-1 活性更高,IC 为 0.11 nM,优于 PM-19 的 4.68 nM。这项研究表明,Keggin 型 POMs 与氨基酸的结合可以成为增强 POMs 抗 HIV-1 生物活性的新策略。所有结果都有望有助于开发更有效和有效的 HIV-1 抑制剂。

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