Abstract
A variety of structurally diverse triphenyltin esters exhibit almost identical in vitro antitumor activity to the potent triphenyltin benzoates and greater activity than cisplatin. This activity is independent of the structure of the ester moiety and comparable to triphenyltin hydroxide, suggesting hydrolysis to a common, cytotoxic tin intermediate.
| Original language | English |
|---|---|
| Pages (from-to) | 165-167 |
| Number of pages | 3 |
| Journal | Main Group Chemistry |
| Volume | 1 |
| Issue number | 1 |
| DOIs | |
| Publication status | Published - 1995 |
| Externally published | Yes |
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Cite this
Tranter, C. J., Berners Price, S. J., Cutts, J., Parsons, P. G., Rintoul, G., & Young, D. J. (1995). A comparison of the potent in vitro antitumor activity of triphenyltin benzoates with that of related tin compounds. Main Group Chemistry, 1(1), 165-167. https://doi.org/10.1080/13583149512331338375