authors |
Brandao, P; Guieu, S; Correia-Branco, A; Silva, C; Martel, F |
nationality |
International |
journal |
INORGANICA CHIMICA ACTA |
author keywords |
Copper(I); Vitamin B-1 derivatives; Thiochrome; Caco-2 cells |
keywords |
COPPER-COMPLEXES SYNTHESIS; METAL-ION INTERACTIONS; CRYSTAL-STRUCTURE; IN-VITRO; STRUCTURAL-CHARACTERIZATION; CYTOTOXIC PROPERTIES; MOLECULAR-STRUCTURE; ANTITUMOR-ACTIVITY; 2 SALTS; THIAMINE |
abstract |
The synthesis and crystal structure of two new copper(I) compounds with molecular formula of {Cu-4[(mu(3)-thiocrome)(2)Cl-4]center dot 2(H2O)}(n) 1, and Cu-2[(mu(2)-thiocrome)(2)Cl-2] 2 are reported. The crystal structure of compounds 1 and 2 are solved by single crystal X-ray diffraction. The reaction of Cu(II) with thiamine chloride in water at room temperature produces Cu(I) thiochrome compounds 1 and 2. Compound 1 shows a 1D chain structure based on the linkage of two crystallographic different copper centers and thiochrome ligand through the N(1), N (2) and N(3) nitrogen atoms. Compound 2 is a 0D dimeric copper structure assembled by two thiochrome ligands. For both compounds, the copper(I) centers exhibits a distorted trigonal pyramidal geometry. The antitumor capacity of both compounds was tested in vitro against a human cancer cell line, the colorectal adenocarcinoma (Caco-2) cell line, by determining their effect on cell viability. The two compounds showed similar IC50 values, and were slightly more potent than cisplatin, against the same cell line. |
publisher |
ELSEVIER SCIENCE SA |
issn |
0020-1693 |
isbn |
1873-3255 |
year published |
2019 |
volume |
487 |
beginning page |
287 |
ending page |
294 |
digital object identifier (doi) |
10.1016/j.ica.2018.12.017 |
web of science category |
Chemistry, Inorganic & Nuclear |
subject category |
Chemistry |
unique article identifier |
WOS:000456799100038
|