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2000
Volume 16, Issue 11
  • ISSN: 1871-5206
  • E-ISSN: 1875-5992

Abstract

In vitro studies with the ruthenium(II) and analogous iridium(III) complexes [Ru(η6- p-cymene)Cl2{Ph2PCH2CH2CH2S(O)xPh-ΚP}], [Ru(η6-p-cymene)Cl{Ph2PCH2CH2CH2S(O)xPh- ΚP,ΚS}][PF6] (1–4), [Ir(η5-C5Me5)Cl2{Ph2PCH2CH2CH2S(O)xPh-ΚP}] and [Ir(η5-C5Me5)Cl{Ph2 PCH2CH2CH2S(O)xPh-ΚP,ΚS}][PF6] (5–8; x = 0, 1) revealed the high selectivity toward the 8505C, A253, MCF-7, SW480 and 518A2 cancer cell lines. Thus, the cationic ruthenium complex 4 proved to be the most selective one. In case of the neutral and cationic ruthenium complexes 1–4 the caspase-dependent apoptotic cell death was proven as the main cause of the drug’s tumoricidal action on 8505C cell line.

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/content/journals/acamc/10.2174/1871520615666151029100749
2016-11-01
2025-05-09
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/content/journals/acamc/10.2174/1871520615666151029100749
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  • Article Type:
    Research Article
Keyword(s): Apoptosis; autophagy; caspase; cisplatin; iridium(III) complexes; ruthenium(II) complexes
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