The synthesis, the structural features and the in vivo biological activity of diorganotin(IV) and triorganotin(IV) derivatives of [mesotetra(4-carboxyphenyl)porphine] (H 4 TPPC) are reported. Derivatives with general formula (R 2 Sn) 2 TPPC and (R 3 Sn) 4 TPPC (R = Me, Bu, and Ph) were obtained, and
Organometallic complexes with biological molecules: XIII. Organotin(IV)[meso-tetra (4-carboxyphenyl)porphinate]s and the cell cycle: a flow-cytometric approach
✍ Scribed by F. Triolo; C. Pellerito; G. C. Stocco; T. Fiore; F. Maggio; L. Pellerito; R. Triolo
- Publisher
- John Wiley and Sons
- Year
- 1999
- Tongue
- English
- Weight
- 138 KB
- Volume
- 13
- Category
- Article
- ISSN
- 0268-2605
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✦ Synopsis
The cytotoxic derivatives diorganotin(IV) and triorganotin(IV) [meso-tetra(4-carboxyphenyl)porphinates, with stoichiometries [R 2 Sn] 2 TPPC and [R 3 Sn] 4 TPPC [R = Me, Bu, Ph; TPPC 4À = meso-tetra(4-carboxyphenyl)porphinate 4À ], namely bis[dimethyltin(IV)], bis[dibutyltin(IV)], bis[diphenyltin(IV)], tetra[trimethyltin(IV)], tetra[tributyltin(IV)] and tetra[triphenyltin(IV)] [meso-tetra(4-carboxyphenyl)porphinate]s, have been used to investigate their effects on the cultured human kidney cell cycle in order to understand further the origin of cell-growth inhibition induced by the above-mentioned chemicals. The cell-cycle-dependent DNA content distribution of cultured cells exposed to these compounds has been analyzed through flow cytometry, a potent technique capable of probing several aspects of drug-induced cytotoxicity. Cultured human kidney cells have been used as a model system, on the premise of greater physiological similarity to the human situation in vivo.
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