TY - JOUR
T1 - Synthesis and cytotoxic characteristics displayed by a series of Ag(i)-, Au(i)- and Au(III)-complexes supported by a common N-heterocyclic carbene
AU - Jhulki, Lalmohan
AU - Dutta, Parul
AU - Santra, Manas Kumar
AU - Cardoso, Marlon H.
AU - Oshiro, Karen G.N.
AU - Franco, Octávio L.
AU - Bertolasi, Valerio
AU - Isab, Anvarhusein A.
AU - Bielawski, Christopher W.
AU - Dinda, Joydev
N1 - Publisher Copyright:
© The Royal Society of Chemistry and the Centre National de la Recherche Scientifique.
PY - 2018
Y1 - 2018
N2 - The synthesis, structures and anticancer studies of a series of precious metal complexes supported by 1-methyl-2-(phenyl)imidazo[1,5-a]pyridine-2-ylidene (1) have been highlighted. The Ag(i) (2), Au(i) (3) and Au(iii) (4) complexes were prepared using standard methods and characterized by a range of techniques, including NMR spectroscopy, X-ray crystallography and elemental analyses. The in vitro cytotoxicity activities displayed by 2-4 were explored against human colon adenocarcinoma (HCT116), lung cancer (A549) and breast cancer (MCF7) cell lines. A series of assays showed that all of the complexes exhibited significant growth inhibition in the aforementioned cell lines. Inspection of the data collected revealed that the Au(i) and Ag(i) complexes were more potent than their Au(iii) congener, a trend that was found to be consistent with molecular docking studies that utilized BCL-2 as a model as this protein regulates cell death through apoptosis.
AB - The synthesis, structures and anticancer studies of a series of precious metal complexes supported by 1-methyl-2-(phenyl)imidazo[1,5-a]pyridine-2-ylidene (1) have been highlighted. The Ag(i) (2), Au(i) (3) and Au(iii) (4) complexes were prepared using standard methods and characterized by a range of techniques, including NMR spectroscopy, X-ray crystallography and elemental analyses. The in vitro cytotoxicity activities displayed by 2-4 were explored against human colon adenocarcinoma (HCT116), lung cancer (A549) and breast cancer (MCF7) cell lines. A series of assays showed that all of the complexes exhibited significant growth inhibition in the aforementioned cell lines. Inspection of the data collected revealed that the Au(i) and Ag(i) complexes were more potent than their Au(iii) congener, a trend that was found to be consistent with molecular docking studies that utilized BCL-2 as a model as this protein regulates cell death through apoptosis.
UR - https://www.scopus.com/pages/publications/85051417396
U2 - 10.1039/c8nj02008f
DO - 10.1039/c8nj02008f
M3 - Article
AN - SCOPUS:85051417396
SN - 1144-0546
VL - 42
SP - 13948
EP - 13956
JO - New Journal of Chemistry
JF - New Journal of Chemistry
IS - 16
ER -