Synthesis and antitumor activity of cyclotriphosphazene-(diamine)platinum(II) conjugates.

Abstract

A new class of water-soluble cyclotriphosphazene-(diamine)platinum(II) conjugate drugs [NP(Am-Li2)(Am.PtA2)]3 (Am: dicarboxylic amino acid; A2: diamine) has been synthesized and characterized by means of elemental analysis, multinuclear (1H, 31P, 13C, 195Pt) NMR and IR spectroscopies. All the title compounds were subjected to both in vitro and in vivo assays against the murine leukemia L1210 cell line and selected human tumor cells. Most of the title compounds have shown higher in vivo antitumor activity than cisplatin and carboplatin, and, in particular, [NP(L-Glu-Li2)(L-Glu.Pt(-dach)]3 (Glu=glutamate, dach=trans(+/-)-1,2-diaminocyclohexane) showed extraordinary high activity (ILS>500%) equally against both parent and cisplatin-resistant leukemia L1210 cell lines. Furthermore, this candidate compound (KI 60606) exhibited a wider spectrum of in vitro activity by showing higher cytotoxicity against all the selected human tumor cells than cisplatin and, therefore, was subjected to preclinical studies which are now near completion.

• Authors: H Baek, Y Cho, C O Lee, Y S Sohn
• Journal: Anti-cancer drugs (Anticancer Drugs) Vol. 11 Issue 9 Pg. 715-25 (Oct 2000) ISSN: 0959-4973 [Print] England
• PMID: 11129734 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)

Chemical References

• Antineoplastic Agents
• KI 60606
• Nitriles
• Organoplatinum Compounds
• Phosphorus Compounds
• cyclotriphosphazene ester

Topics

• Animals
• Antineoplastic Agents (chemical synthesis, pharmacology)
• Drug Screening Assays, Antitumor
• Humans
• Leukemia L1210 (drug therapy)
• Magnetic Resonance Spectroscopy
• Mice
• Nitriles (chemical synthesis, pharmacology)
• Organoplatinum Compounds (chemical synthesis, pharmacology)
• Phosphorus Compounds (chemical synthesis, pharmacology)
• Tumor Cells, Cultured (drug effects)