Köckerbauer, Reinhold and Bednarski, Patrick J. (1996) Unusual reactivity of cisplatin analogs that bear o-phenylenediamine ligands: Insights for the design of more effective cytotoxic agents. JOURNAL OF INORGANIC BIOCHEMISTRY, 62 (4). pp. 281-298. ISSN 0162-0134
Full text not available from this repository.Abstract
The stabilities of dichloro(o-phenylenediamine)platinum(II) (1) and several 4,5-disubstituted analogs [i.e., with: Cl (2), Br (3), Me (4), or MeO (5)] were investigated under various aqueous conditions. The Pt complexes 1-5 decomposed by reactions which were independent of the amount of chloride in the medium. The poor aqueous stabilities of 1-5 were attributed to two factors: 1) The compounds underwent facile oxidation reactions in aqueous solution at pH 7.4 and 37 degrees C, resulting in the formation of intensely colored Pt-species as well as H2O2. Compounds 2 and 3 oxidized considerably faster than 1, 4, and 5. Based on the redox behavior and UV-Vis spectra of the decomposition products, it is proposed that they are o-benzoquinonediimine Pt complexes. 2) Compound 4 underwent an unusually rapid substitution reaction with L-methionine, a component of the culture medium, whereby both of the chloro ligands of platinum were replaced by an N,S-chelated methionine. At an L-methionine concentration of 0.5 mM, the reaction ran to completion within 1 min. Thus, the weak growth inhibitory activities of 1-5 on human cancer cells in vitro was likely a result of their poor chemical stability in the culture medium. Based on a knowledge of the decomposition pathways, analogs were designed to be resistant to these types of reactions. Dichloro(o-aminomethylaniline)platinum(II) (6) and [bis-1,2(aminomethyl)benzene]-dichloroplatinum(II) (7) were synthesized and their aqueous stabilities investigated. Both 6 and 7 were considerably more stable than 1-5 under aqueous conditions, as well as being more effective in inhibiting the growth of human cancer cells in vitro.
Item Type: | Article |
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Uncontrolled Keywords: | MIXED-AMINE CISPLATIN; AQUEOUS CHEMISTRY; COMPLEXES; METABOLITES; METHIONINE; INVITRO |
Subjects: | 600 Technology > 615 Pharmacy |
Divisions: | Chemistry and Pharmacy > Institute of Pharmacy |
Depositing User: | Dr. Gernot Deinzer |
Date Deposited: | 06 Jul 2023 04:49 |
Last Modified: | 06 Jul 2023 04:49 |
URI: | https://pred.uni-regensburg.de/id/eprint/51676 |
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