sodium;azane;dichloroplatinum;chloride | 101151-57-9

• 分子结构分类: 无机化合物 - 混合金属/非金属化合物
• 英文名称: sodium;azane;dichloroplatinum;chloride
• CAS: 101151-57-9
• 化学式: Cl₃H₃NPt*Na
• 分子量: 341.459
• InChiKey: GEDVRPXYXGDEOZ-UHFFFAOYSA-K

计算性质

• 辛醇/水分配系数(LogP)：
  None
• 重原子数：
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• 可旋转键数：
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• 环数：
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• sp3杂化的碳原子比例：
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• 拓扑面积：
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• 氢给体数：
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• 氢受体数：
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反应信息

• 作为反应物：
  描述：

  sodium;azane;dichloroplatinum;chloride 、 3-氨基-2,2,5,5-四甲基-1-吡咯烷酮 、 sodium iodide 以 水 为溶剂， 以63%的产率得到cis-ammine(3-amino-2,2,5,5-tetramethylpyrrolidin-1-oxyl)iodochloroplatinum (II)
  参考文献：
  名称：

  Synthesis, structure, and biological activity of mixed-ligand platinum(II) complexes with aminonitroxides

  摘要：

  Mixed-ligand platinum complexes cis-Pt-11((RNH2)-N-6)(NH3)X-2 and cis-Pt-11((RNH2)-N-5)(NH3)X-2 (R-6 is 2,2,6,6-tetramethyl-4-piperidyl-1-oxyl and R-5 is 2,2,5,5-tetramethyl-3-pyrrolidinyl-1-oxyl) were synthesized by either the reaction of aminonitroxides RNH2 with Na[Pt-11(NH3)CI2I] generated in situ (for X-2 = ClI) or by replacement of the iodo-chloro ligands in Cis-Pt-11(RNH2)(NH3)Cll by dichloro and oxalato ligands. The complexes obtained were characterized by elemental analysis and by IR, UV, and ESR spectra. For Cis-Pt-11((RNH2)-N-5)(NH3)Cl-2, crystal and molecular structures were determined by X-ray diffraction analysis. Cisplatin accelerates autooxidation of methyl linoleate and the platinum nitroxide complexes synthesized exhibit antioxidant properties. The rate of isolated DNA binding with the new complexes is almost as high as that for cisplatin. cis-Pt-11((RNH2)-N-6)(NH3)Cl-2 exhibits the highest antitumor activity. The high antitumor activity of platinum nitroxide complexes shows that the possible "radical component" is not a crucial factor in the cytotoxic action of cisplatin.

  DOI：

  10.1007/bf02495168

文献信息

• ——
  作者：V. D. Sen""

  DOI：10.1023/a:1023475319835

  日期：——

  The platinum(IV) complexes cis,trans,cis-Pt-IV(RNH2)(NH3)(OH)(2)Cl-2, where R is 2,2,6,6-tetramethyl-1-oxyl-4-piperidinyl (1) or 2,2,5,5-tetramethyl-1-oxyl-3-pyrrolidinyl (2), were prepared by oxidation of the corresponding cis-Pt-II(RNH2)(NH3)Cl-2 complexes with hydrogen peroxide. The reactions are catalyzed by tungstate salts, which makes it possible to carry out oxidation under mild conditions. The resulting complexes were characterized by elemental analysis, HPLC, and IR, UV, and ESR spectroscopy. The structure of complex 1 was established by X-ray diffraction analysis. Complex 1 exhibits the highest antitumor activity in an experimental tumor, viz., in P388 leukemia. The resistance of the tumor to this complex developed much slower than that to Cisplatin.
• ——
  作者：V. D. Sen"、A. V. Shugalii、A. V. Kulikov

  DOI：10.1023/a:1019686323902

  日期：——

  The mixed-ligand complexes cis-Pt-11[R(CH2),NH2](NH3)X-2, where R = 2,2,6,6-tetramethyl-1-oxylpiperidin-4-yl, X-2 = ClI or Cl-2, n = 1 or 2, and binuclear complexes trans-3,4-bis[cis-ammine (iodochloro or dichloro)platinum(II)amino]-2,2,6,6-tetramethylpiperidin-1-oxyls were synthesized. The reactivity of the aminonitroxide complexes toward DNA, the destabilizing effect of the adducts on DNA structure, and the distribution of the Pt adducts along the DNA duplex were studied. The platination activity of the complexes is affected by the natures of both the leaving ligands X and the carrying amino ligands. The decrease in the platination activity of the complexes with an increase in the amino ligand sizes is probably caused by steric hindrance. The complexes that effectively platinate isolated DNA and cause a moderate destabilizition of DNA duplex possess high antitumor activities.