Alkynyl(triphenylphosphine)gold(I) complexes carrying variously substituted propargylic amines have been synthesized and fully characterized in solution and solid state. High levels of toxicity (i.e. micromolar range) were recognized for a series of cancer cell lines with particular emphasis on HT29, IGROV1, HL60 and I407. In particular the lead compound 3ab was identified as the most active compound in all cell lines (IC50: 1.7–7.9 μM).
De Nisi, A., Bergamini, C., Leonzio, M., Sartor, G., Fato, R., Naldi, M., et al. (2016). Synthesis, cytotoxicity and anti-cancer activity of new alkynyl-gold(I) complexes. DALTON TRANSACTIONS, 45, 1546-1553 [10.1039/c5dt02905h].
Synthesis, cytotoxicity and anti-cancer activity of new alkynyl-gold(I) complexes
DE NISI, ASSUNTAMethodology
;BERGAMINI, CHRISTIANMethodology
;SARTOR, GIORGIOMethodology
;FATO, ROMANAConceptualization
;NALDI, MARINAMethodology
;MONARI, MAGDAConceptualization
;CALONGHI, NATALIAConceptualization
;BANDINI, MARCO
Writing – Original Draft Preparation
2016
Abstract
Alkynyl(triphenylphosphine)gold(I) complexes carrying variously substituted propargylic amines have been synthesized and fully characterized in solution and solid state. High levels of toxicity (i.e. micromolar range) were recognized for a series of cancer cell lines with particular emphasis on HT29, IGROV1, HL60 and I407. In particular the lead compound 3ab was identified as the most active compound in all cell lines (IC50: 1.7–7.9 μM).| File | Dimensione | Formato | |
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Synthesis, cytotoxicity and anti-cancer .pdf
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