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基于聚氮杂大环的双金(I)和四金(I)膦二硫代氨基甲酸酯配合物的快速合成及抗增殖性能。

Rapid Synthesis and Antiproliferative Properties of Polyazamacrocycle-Based Bi- and Tetra-Gold(I) Phosphine Dithiocarbamate Complexes.

机构信息

CNRS, Université Bourgogne Franche-Comté, ICMUB UMR6302, 9 avenue Alain Savary, 21000, Dijon, France.

Université de Nantes, UFR Sciences Pharmaceutiques, Laboratoire IIciMed EA1155, Département de Cancérologie, 9 rue Bias, 44035, Nantes, France.

出版信息

Chembiochem. 2019 Sep 2;20(17):2255-2261. doi: 10.1002/cbic.201900227. Epub 2019 Jul 19.

Abstract

A family of bi- and tetrametallic gold(I) phosphine dithiocarbamate complexes were synthesized, starting from cyclam and dimethylcyclam polyazamacrocycles, respectively, along with their monometallic gold(I) chloridophosphine precursors. Their antiproliferative properties were evaluated on two cancer cell lines (A549 and NSCLC-N6-L16). Most of the mono- and bimetallic complexes displayed strong activities and, in particular, one bimetallic derivative showed antiproliferative properties in the low micromolar range. Insights into the structure-activity relationships are given, along with determination of the thioredoxin reductase inhibition potential, two-photon imaging of the fluorescent derivatives, and evaluation of gold uptake.

摘要

合成了一系列双金属和四金属金(I)膦二硫代氨基甲酸盐配合物,分别以环烷和二甲基环烷多氮大环为起始物,并与它们的单金属金(I)氯化磷前体一起。在两种癌细胞系(A549 和 NSCLC-N6-L16)上评估了它们的抗增殖特性。大多数单核和双核配合物表现出很强的活性,特别是一种双核衍生物在低微摩尔范围内表现出抗增殖活性。给出了结构-活性关系的见解,包括测定硫氧还蛋白还原酶抑制潜力、荧光衍生物的双光子成像以及金摄取的评估。

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