70618-23-4Relevant academic research and scientific papers
Chemistry of ruthenium(II) complexes of the tridentate NNS donor methyl 2-pyridyl ketone 4-(4-tolyl)thiosemicarbazone. Isolation and structural characterisation of a novel rutheniuni(II) complex containing a co-ordinated imine of an α-N heterocyclic keton
Maji, Milan,Chatterjee, Madhumita,Ghosh, Saktiprosad,Chattopadhyay, Shyamal Kumar,Wu, Bo-Mu,Mak, Thomas C. W.
, p. 135 - 140 (1999)
A series of ruthenium(II) complexes of the NNS donor ligand methyl 2-pyridyl ketone 4-(4-tolyl)thiosemicarbazone (HL) has been synthesized using RuCl3·xH2O and [Ru(PPh3)3Cl2]: [Ru(HL)2][ClO
Design, synthesis and biological evaluation of thiosemicarbazones, hydrazinobenzothiazoles and arylhydrazones as anticancer agents with a potential to overcome multidrug resistance
Pape, Veronika F.S.,Tóth, Szilárd,Füredi, András,Szebényi, Kornélia,Lovrics, Anna,Szabó, Pál,Wiese, Michael,Szakács, Gergely
, p. 335 - 354 (2016/05/19)
There is a constant need for new therapies against multidrug resistant (MDR) cancer. An attractive strategy is to develop chelators that display significant antitumor activity in multidrug resistant cancer cell lines overexpressing the drug efflux pump P-glycoprotein. In this study we used a panel of sensitive and MDR cancer cell lines to evaluate the toxicity of picolinylidene and salicylidene thiosemicarbazone, arylhydrazone, as well as picolinylidene and salicylidene hydrazino-benzothiazole derivatives. Our results confirm the collateral sensitivity of MDR cells to isatin-β-thiosemicarbazones, and identify several chelator scaffolds with a potential to overcome multidrug resistance. Analysis of structure-activity-relationships within the investigated compound library indicates that NNS and NNN donor chelators show superior toxicity as compared to ONS derivatives regardless of the resistance status of the cells.
