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基于1,2,4 -三嗪的生物相容性配体与选定3d金属离子的配位化合物的合成、表征及生物筛选

Synthesis, characterization, and biological screening of coordination compounds with 1,2,4-triazine based biocompatible ligands and selected 3d-metal ions.

作者信息

Ammal P Rugmini, Prasad Anupama R, Joseph Abraham

机构信息

Department of Chemistry, Zamorin's Guruvayurappan College, Calicut, India.

Department of Chemistry, University of Calicut, Kerala, India.

出版信息

Heliyon. 2020 Oct 6;6(10):e05144. doi: 10.1016/j.heliyon.2020.e05144. eCollection 2020 Oct.

DOI:10.1016/j.heliyon.2020.e05144
PMID:33083609
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7553991/
Abstract

A bidentate Schiff base ligand, MHMMT, obtained from 1,2,4-triazine derivative and 4-hydroxy-3-methoxy benzaldehyde and its Fe(III), Co(II), Ni(II), Cu(II), and Zn(II) complexes were synthesised in ethanolic media and characterized by various analytical techniques like elemental analyses, magnetic susceptibility measurements, FTIR, UV-VIS, proton NMR, ESR, spectroscopic and thermogravimetric studies. Various geometries like a tetrahedral for Co(II) and Zn(II) complexes, an octahedral for Fe(III) and Ni(II) complexes, and square planar for Cu(II) complex has been assigned. For all metals complexes except Co(II), a 2:1 ligand to metal ratio is observed, while Co(II) complex has a 1:1 ratio. In accordance with the probable activity spectra of substances as obtained from PASS analysis, α-amylase inhibition studies by starch-iodine method for ligand and complexes except that of Fe(III) and anticancer screening against human breast cancer cell lines MCF-7 using MTT assay for Fe(III) complex were conducted. The tested compounds were found to be good α-amylase inhibitors, characteristically similar to most of the antidiabetic drugs. Among the compounds, Cu(II) complex exhibited the highest α-amylase inhibitory activity. Furthermore, ligand and complexes were also exposed to antimicrobial activities, drug-likeness, bioactivity score prediction by Molinspiration software. Molecular docking analysis of selected compounds on α-amylase and VEGFR-2 kinase were carried out for confirming the experimental observations.

摘要

一种双齿席夫碱配体MHMMT,由1,2,4 -三嗪衍生物和4 -羟基-3 -甲氧基苯甲醛制得,其铁(III)、钴(II)、镍(II)、铜(II)和锌(II)配合物在乙醇介质中合成,并通过元素分析、磁化率测量、傅里叶变换红外光谱(FTIR)、紫外可见光谱(UV - VIS)、质子核磁共振(NMR)、电子顺磁共振(ESR)、光谱和热重分析等多种分析技术进行表征。已确定各种几何构型,如钴(II)和锌(II)配合物为四面体构型,铁(III)和镍(II)配合物为八面体构型,铜(II)配合物为平面正方形构型。除钴(II)外,所有金属配合物的配体与金属比例均为2:1,而钴(II)配合物的比例为1:1。根据通过PASS分析获得的物质可能的活性谱,采用淀粉-碘法对配体和除铁(III)配合物外的其他配合物进行α-淀粉酶抑制研究,并采用MTT法对铁(III)配合物进行抗人乳腺癌细胞系MCF - 7的抗癌筛选。测试的化合物被发现是良好的α-淀粉酶抑制剂,其特性与大多数抗糖尿病药物相似。其中,铜(II)配合物表现出最高的α-淀粉酶抑制活性。此外,还通过Molinspiration软件对配体和配合物进行了抗菌活性、类药性、生物活性评分预测。对选定化合物在α-淀粉酶和血管内皮生长因子受体-2激酶(VEGFR - 2 kinase)上进行分子对接分析,以证实实验观察结果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c6dd/7553991/c4ea18257df9/gr12.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c6dd/7553991/a89b2d7bb21b/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c6dd/7553991/8bc002349057/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c6dd/7553991/c8bdb2ab0a32/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c6dd/7553991/daa6d0a0afa9/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c6dd/7553991/3f495a0388a9/gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c6dd/7553991/2a3c28526126/gr6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c6dd/7553991/e101abb5cc28/gr7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c6dd/7553991/73113c650815/gr8.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c6dd/7553991/e07d62250733/gr9.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c6dd/7553991/fcbbd6483137/gr10.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c6dd/7553991/c26b5b5f79a0/gr11.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c6dd/7553991/c4ea18257df9/gr12.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c6dd/7553991/a89b2d7bb21b/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c6dd/7553991/8bc002349057/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c6dd/7553991/c8bdb2ab0a32/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c6dd/7553991/daa6d0a0afa9/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c6dd/7553991/3f495a0388a9/gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c6dd/7553991/2a3c28526126/gr6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c6dd/7553991/e101abb5cc28/gr7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c6dd/7553991/73113c650815/gr8.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c6dd/7553991/e07d62250733/gr9.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c6dd/7553991/fcbbd6483137/gr10.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c6dd/7553991/c26b5b5f79a0/gr11.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c6dd/7553991/c4ea18257df9/gr12.jpg

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