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含双(吡唑-1-基)-和双(三唑-1-基)-乙酸根异硫氰酸酯配体的 Cu(II) 配合物的合成与生物研究。

Syntheses and Biological Studies of Cu(II) Complexes Bearing Bis(pyrazol-1-yl)- and Bis(triazol-1-yl)-acetato Heteroscorpionate Ligands.

机构信息

School of Science and Technology, Chemistry Division, University of Camerino, via S. Agostino 1, 62032 Camerino, Macerata, Italy.

Department of Pharmaceutical and Pharmacological Sciences, University of Padova, via Marzolo 5, 35131 Padova, Italy.

出版信息

Molecules. 2019 May 7;24(9):1761. doi: 10.3390/molecules24091761.

DOI:10.3390/molecules24091761
PMID:31067640
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6539868/
Abstract

Copper(II) complexes of bis(pyrazol-1-yl)- and bis(triazol-1-yl)-acetate heteroscorpionate ligands have been synthesized. The copper(II) complexes [HC(COOH)(pz)]Cu[HC(COO)(pz)]·ClO, [HC(COOH)(pz)]Cu(ClO) (pz = 3,5-dimethylpyrazole; pz = pyrazole) were prepared by the reaction of Cu(ClO)·6HO with bis(3,5-dimethylpyrazol-1-yl)acetic acid (HC(COOH)(pz)) and bis(pyrazol-1-yl)acetic acid (HC(COOH)(pz)) ligands in ethanol solution. The copper(II) complex [HC(COOH)(tz)]Cu(ClO)·CHOH (tz = 1,2,4-triazole) was prepared by the reaction of Cu(ClO)·6HO with bis(1,2,4-triazol-1-yl)acetic acid (HC(COOH)(tz)) ligand in methanol solution. The synthesized Cu(II) complexes, as well as the corresponding uncoordinated ligands, were evaluated for their cytotoxic activity in monolayer and 3D spheroid cancer cell cultures with different Pt(II)-sensitivity. The results showed that [HC(COOH)(pz)]Cu[HC(COO)(pz)]·ClO was active against cancer cell lines derived from solid tumors at low IC and this effect was retained in the spheroid model. Structure and ultra-structure changes of treated cancer cells analyzed by Transmission Electron Microscopy (TEM) highlighted the induction of a cytoplasmic vacuolization, thus suggesting paraptotic-like cancer cell death triggering.

摘要

合成了双(吡唑-1-基)和双(三唑-1-基)乙酸酯异硫氰酸酯配合物的铜(II)配合物。通过将 Cu(ClO)·6HO 与双(3,5-二甲基吡唑-1-基)乙酸(HC(COOH)(pz))和双(吡唑-1-基)乙酸(HC(COOH)(pz))配体在乙醇溶液中反应,制备了铜(II)配合物 [HC(COOH)(pz)]Cu[HC(COO)(pz)]·ClO 和 [HC(COOH)(pz)]Cu(ClO)(pz = 3,5-二甲基吡唑;pz = 吡唑)。通过将 Cu(ClO)·6HO 与双(1,2,4-三唑-1-基)乙酸(HC(COOH)(tz))配体在甲醇溶液中反应,制备了铜(II)配合物 [HC(COOH)(tz)]Cu(ClO)·CHOH(tz = 1,2,4-三唑)。合成的 Cu(II)配合物以及相应的未配位配体在单层和具有不同 Pt(II)敏感性的 3D 球体癌细胞培养物中评估了它们的细胞毒性活性。结果表明,[HC(COOH)(pz)]Cu[HC(COO)(pz)]·ClO 对源自实体瘤的癌细胞系具有低 IC 的活性,并且这种作用在球体模型中得以保留。通过透射电子显微镜(TEM)分析处理后的癌细胞的结构和超微结构变化,突出了细胞质空泡化的诱导,从而提示类似细胞凋亡的癌细胞死亡触发。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2df1/6539868/2ed23a5b79b2/molecules-24-01761-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2df1/6539868/081b4b6d264d/molecules-24-01761-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2df1/6539868/97d4ad3b4cd9/molecules-24-01761-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2df1/6539868/4836e00fd73c/molecules-24-01761-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2df1/6539868/baf36c8d49cd/molecules-24-01761-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2df1/6539868/fd9b258bf606/molecules-24-01761-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2df1/6539868/c2f4d12b8e04/molecules-24-01761-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2df1/6539868/2ed23a5b79b2/molecules-24-01761-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2df1/6539868/081b4b6d264d/molecules-24-01761-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2df1/6539868/97d4ad3b4cd9/molecules-24-01761-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2df1/6539868/4836e00fd73c/molecules-24-01761-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2df1/6539868/baf36c8d49cd/molecules-24-01761-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2df1/6539868/fd9b258bf606/molecules-24-01761-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2df1/6539868/c2f4d12b8e04/molecules-24-01761-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2df1/6539868/2ed23a5b79b2/molecules-24-01761-g007.jpg

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