Designing new iridium(iii) arene complexes of naphthoquinone derivatives as anticancer agents: a structure–activity relationship study. Issue 7 (31st January 2017)
- Record Type:
- Journal Article
- Title:
- Designing new iridium(iii) arene complexes of naphthoquinone derivatives as anticancer agents: a structure–activity relationship study. Issue 7 (31st January 2017)
- Main Title:
- Designing new iridium(iii) arene complexes of naphthoquinone derivatives as anticancer agents: a structure–activity relationship study
- Authors:
- Tabrizi, Leila
Chiniforoshan, Hossein - Abstract:
- Abstract : A series of iridium(iii ) arene complexes of naphthoquinone derivatives have been synthesized and investigated for their suitability as potential anticancer drugs. Abstract : A series of iridium(iii ) arene complexes of naphthoquinone derivatives of the formula [Ir III (η 6 -L1)(L2)(3, 5-(NO2 )2 pcyd)](PF6 ) (L1 = p -methylphenyl)ethynylferrocene; L2 = Lap: lapachol, 1, Plum: plumbagin, 2, Law: lawsone, 3, and Jug: juglone, 4 ; 3, 5-(NO2 )2 pcyd = 3, 5-dinitrophenylcyanamide) have been synthesized and investigated for their suitability as potential anticancer drugs. The DNA-binding interactions of the complexes with calf thymus DNA have been studied by absorption, emission, and viscosity measurements. Their cytotoxicity against the cancer cell lines including colon adenocarcinoma (HT-29), liver hepatocellular carcinoma (HepG-2), breast (MCF-7), colon carcinoma (HCT-8), and ovary (A2780) is reported. Remarkably, almost all complexes exhibit significant cytotoxic effects towards HepG-2, MCF-7, and HCT-8 cancer cell lines and complex1 emerged as the most cytotoxic derivative in comparison with other complexes. The complexes1–4 increase the production of reactive oxygen species (ROS) in MCF-7 cells. The new compounds also inhibit the enzyme thioredoxin reductase activity at nanomolar concentrations. Furthermore, the complexes induce major levels of cancer cell death by apoptosis that is in correlation with activity in cytotoxicity studies.
- Is Part Of:
- Dalton transactions. Volume 46:Issue 7(2017)
- Journal:
- Dalton transactions
- Issue:
- Volume 46:Issue 7(2017)
- Issue Display:
- Volume 46, Issue 7 (2017)
- Year:
- 2017
- Volume:
- 46
- Issue:
- 7
- Issue Sort Value:
- 2017-0046-0007-0000
- Page Start:
- 2339
- Page End:
- 2349
- Publication Date:
- 2017-01-31
- Subjects:
- Chemistry, Inorganic -- Periodicals
Chemistry, Physical and theoretical -- Periodicals
Chemistry, Inorganic -- Periodicals
546.05 - Journal URLs:
- http://pubs.rsc.org/en/journals/journalissues/dt#!issueid=dt043040&type=current&issnprint=1477-9226 ↗
http://www.rsc.org/ ↗ - DOI:
- 10.1039/c6dt04339a ↗
- Languages:
- English
- ISSNs:
- 1477-9226
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3517.830000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 1977.xml