Journal article
The in vitro Antitumour Activity of Substituted Dibutyl-1,3,2-dioxastannolanes
Applied Organometallic Chemistry, Vol.11(7), pp.577-581
1997
Abstract
Six dibutyl-l,3,2-dioxastannolanes, including two enantiomeric pairs, exhibited greater in vitro antitumour activity towards a variety of human tumour cell lines than cisplatin but with little discrimination, suggesting hydrolysis to a common cytotoxic intermediate. A cell line hypersensitive to mitochondrial inhibitors (CI80-13S) was not sensitive to any of the test compounds, suggesting that cell mechanisms other than, or in addition to, mitochondrial function are targeted by tin antitumour agents. A pigmented melanoma cell line (MM418c5) was resistant to the test compounds, which were found to be sequestered by melanin. This resistance was not observed with triphenyltin hydroxide. © 1997 by John Wiley & Sons, Ltd.
Details
- Title
- The in vitro Antitumour Activity of Substituted Dibutyl-1,3,2-dioxastannolanes
- Authors
- S C Ng (Author) - National University of Singapore, SingaporeP G Parsons (Author) - Queensland Institute of Medical ResearchK Y Sim (Author) - National University of Singapore, SingaporeC J Tranter (Author) - Griffith UniversityRodney H White (Author) - Griffith UniversityDavid James Young (Author) - Griffith University
- Publication details
- Applied Organometallic Chemistry, Vol.11(7), pp.577-581
- Publisher
- John Wiley & Sons Ltd.
- DOI
- 10.1002/(SICI)1099-0739(199707)11:7<577::AID-AOC612>3.0.CO;2-S
- ISSN
- 0268-2605
- Organisation Unit
- University of the Sunshine Coast, Queensland
- Language
- English
- Record Identifier
- 99449831802621
- Output Type
- Journal article
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