2020
DOI: 10.2147/dddt.s275007
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<p>Ruthenium Complexes as Anticancer Agents: A Brief History and Perspectives</p>

Abstract: Platinum (Pt)-based anticancer drugs such as cisplatin have been used to treat various cancers. However, they have some limitations including poor selectivity and toxicity towards normal cells and increasing chemoresistance. Therefore, there is a need for novel metallo-anticancers, which has not been met for decades. Since the initial introduction of ruthenium (Ru) polypyridyl complex, a number of attempts at structural evolution have been conducted to improve efficacy. Among them, half-sandwich Ru-arene compl… Show more

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Cited by 256 publications
(173 citation statements)
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“…Ruthenium complexes have been extensively reported as potent cytotoxic and anti-metastatic agents in different cancer cells ( 52 , 53 ); however, the incorporation of bioactive ligands enhances the biological activity of the metal complex formed. Ruthenium(II) complexes designed in the present study were tested against several cancer cells, presenting important cytotoxic activity.…”
Section: Discussionmentioning
confidence: 99%
“…Ruthenium complexes have been extensively reported as potent cytotoxic and anti-metastatic agents in different cancer cells ( 52 , 53 ); however, the incorporation of bioactive ligands enhances the biological activity of the metal complex formed. Ruthenium(II) complexes designed in the present study were tested against several cancer cells, presenting important cytotoxic activity.…”
Section: Discussionmentioning
confidence: 99%
“…Ruthenium complexes are of interest as catalysts, and they have also emerged as promising nonplatinum antitumor or antimetastatic agents [1][2][3][4][5][6]. A great number of ruthenium complexes with potential antitumor activity have been developed to date.…”
Section: Introductionmentioning
confidence: 99%
“…Even though from the thermodynamic point of view, a Pt-ligand bond in conventional platinum(II) coordination compounds presents somewhat lower thermodynamic durability (≤100 kJ/mol) than single and double covalent bonds between C–C, C–N or C–O (250–500 kJ/mol), the ligand substitution is rather slow, yielding reasonably stable molecules with desired in vivo pharmacokinetic and pharmacodynamic properties [ 10 , 11 ]. In addition to numerous platinum compounds developed in recent decades [ 9 ], complexes containing other transition metals have also been investigated, including palladium(II) [ 12 ], gold(I), gold(II), tin(IV) [ 13 ], ruthenium(II), ruthenium(III) [ 14 ] and copper(II)-based compounds [ 15 ]. Palladium(II) complexes have received particular interest as potential Pt(II) analogs thanks to the similarities in structure and coordination chemistry between these two metal ions [ 12 , 16 ].…”
Section: Introductionmentioning
confidence: 99%