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首页> 外文期刊>Inorganic Chemistry Communications >Syntheses, crystal structures and anticancer activities of three novel transition metal complexes with Schiff base derived from 2-acetylpyridine and 1-tryptophan
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Syntheses, crystal structures and anticancer activities of three novel transition metal complexes with Schiff base derived from 2-acetylpyridine and 1-tryptophan

机译:三种由2-乙酰吡啶和1-色氨酸衍生的席夫碱的新型过渡金属配合物的合成,晶体结构和抗癌活性

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Three novel transition metal coordination complexes, Cu(C_(18)H_(16)N3O2)2·2CH3OH (1), Zn(C_(18)H_(16)N3O2)2·2-CH3CH2OH (2) and Cd(C_(18)H_(16)N3O2)2·2CH3OH (3) (C_(18)H_(16)N3O2: 2-acetylpyridine-L-tryptophan) have been synthesized and characterized by IR, UV, elemental analysis,~1H NMR and X-ray diffraction single crystal analysis. The three crystals crystallize in the tetragonal crystal system, space group P432_12. They are all six-coordinated by two nitrogen atoms from C=N, two nitrogen atoms from pyridine rings and two carboxylic oxygen atoms in different ligands, forming a distorted octahedron geometry. Each ligand serves as a bridging ligand to link metal ions through carboxylic oxygen atoms, leading to a three-dimensional coordination polymer. The anticancer activities of these three complexes on MDA-MB-231 breast cancer cells were also investigated. The results indicate that all of the three complexes can inhibit the cellular proliferation. Furthermore, Cd(C_(18)H_(16)N3O2)2·2CH3OH (3) has the highest anti-proliferative activity among the three complexes. In addition, Cd(C_(18)H_(16)N3O2)2 · 2CH3OH (3) can inhibit proteasomal chymotrypsin-like activity and also can induce apoptosis on human breast cancer MDA-MB-231 cells.
机译:三种新型过渡金属配位化合物Cu(C_(18)H_(16)N3O2)2·2CH3OH(1),Zn(C_(18)H_(16)N3O2)2·2-CH3CH2OH(2)和Cd(C_ (18)H_(16)N3O2)2·2CH3OH(3)(C_(18)H_(16)N3O2:2-乙酰吡啶-L-色氨酸)已经合成并通过红外,紫外,元素分析和〜1H NMR表征和X射线衍射单晶分析。这三种晶体在四方晶系空间群P432_12中结晶。它们全都由来自C = N的两个氮原子,来自吡啶环的两个氮原子和不同配体中的两个羧基氧原子进行六配位,形成扭曲的八面体几何形状。每个配体用作桥接配体,以通过羧基氧原子连接金属离子,从而形成三维配位聚合物。还研究了这三种复合物对MDA-MB-231乳腺癌细胞的抗癌活性。结果表明,所有三种复合物均可抑制细胞增殖。此外,Cd(C_(18)H_(16)N3O2)2·2CH3OH(3)在这三种配合物中具有最高的抗增殖活性。此外,Cd(C_(18)H_(16)N3O2)2·2CH3OH(3)可以抑制蛋白酶体胰凝乳蛋白酶样活性,还可以诱导人乳腺癌MDA-MB-231细胞凋亡。

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