Synthesis of Pt(II) Complexes Containing D-Glucuronate, D-Gluconate, or Their Acetyl Derivatives and Evaluation of Antitumor Activity against Murine Leukemia L1210
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- 野路 雅英
- Faculty of Pharmaceutical Sciences, Nagoya City University
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- 花井 元子
- Faculty of Pharmaceutical Sciences, Nagoya City University
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- 大森 敬之
- Faculty of Pharmaceutical Sciences, Nagoya City University
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- 田代 田鶴子
- Cancer Chemotherapy Center, Japanese Foundation for Cancer Research
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- 鈴木 憲治郎
- Department of Pharmacy, Tokai Teishin Hospital
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- 喜谷 喜徳
- Faculty of Pharmaceutical Sciences, Nagoya City University
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New antitumor-active Pt(II) complexes of (1R, 2R)-cyclohexanediamine (=(1R, 2R)-dach) and 2-(aminomethyl)cyclohexylamine (=amcha) isomers containing D-glucuronate, D-gluconate, tetra-O-acetylglucuronate (=Ac_4-glucuronate) or tetra-O-acetylgluconate (=Ac_4-gluconate) as a leaving group were synthesized. The structures of the Pt(II) complexes were determined by analyzing the infrared and ^<13>C-nuclear magnetic resonance spectra and it was concluded that these leaving groups coordinate to the central Pt(II) ions through the carboxyl groups. Antitumor activities of the Pt(II) complexes were tested against murine leukemia L1210 according to the protocol of the National Cancer Institute (Bethesda, Md.). All the Pt(II) complexes synthesized were antitumor-active. In particular, water-soluble Pt(gluconato)(NO_3)(cis-amcha) and lipo-soluble Pt(Ac_4-β-glucuronato)_2-((1R, 2R)-dach) exhibited excellent antitumor activity, giving T/C% values of 317 and 388,respectively, each with four cured mice out of six at a dose of 50 mg/kg. These two Pt(II) complexes are considered to be worthy of further development.
収録刊行物
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- Chemical & pharmaceutical bulletin
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Chemical & pharmaceutical bulletin 36 (9), 3439-3446, 1988-09-25
公益社団法人日本薬学会
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詳細情報 詳細情報について
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- CRID
- 1570009752553171840
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- NII論文ID
- 110003654824
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- NII書誌ID
- AA00602100
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- ISSN
- 00092363
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- 本文言語コード
- en
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- データソース種別
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- CiNii Articles