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trans-[Pt(S-4,6-dimethylpyrimidine-2-thionate)2(PTA)2] | 1436404-93-1

中文名称
——
中文别名
——
英文名称
trans-[Pt(S-4,6-dimethylpyrimidine-2-thionate)2(PTA)2]
英文别名
trans-[Pt(S-4,6-dimethylpyrimidine-2-thionate)2(1,3,5-triaza-7-phosphaadamantane)2]
trans-[Pt(S-4,6-dimethylpyrimidine-2-thionate)<sub>2</sub>(PTA)<sub>2</sub>]化学式
CAS
1436404-93-1
化学式
C24H38N10P2PtS2
mdl
——
分子量
787.792
InChiKey
JGFVZSCGLGWNFV-UHFFFAOYSA-L
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

计算性质

  • 辛醇/水分配系数(LogP):
    2.32
  • 重原子数:
    39.0
  • 可旋转键数:
    6.0
  • 环数:
    10.0
  • sp3杂化的碳原子比例:
    0.67
  • 拓扑面积:
    71.0
  • 氢给体数:
    0.0
  • 氢受体数:
    12.0

反应信息

  • 作为产物:
    描述:
    4,6-二甲基-2-巯基嘧啶cis-[PtCl2(1,3,5-triaza-7-phosphaadamantane)2]sodium ethanolate 作用下, 以 乙醇 为溶剂, 反应 24.0h, 以83%的产率得到trans-[Pt(S-4,6-dimethylpyrimidine-2-thionate)2(PTA)2]
    参考文献:
    名称:
    trans-Thionate Derivatives of Pt(II) and Pd(II) with Water-Soluble Phosphane PTA and DAPTA Ligands: Antiproliferative Activity against Human Ovarian Cancer Cell Lines
    摘要:
    A series of PTA and DAPTA platinum(II) and palladium(II) thionate complexes of the type trans-[M(SN)(2)P-2] were prepared from the reaction of cis-[MCl2P2] [M = Pt, Pd; P = PTA (1,3,5-triaza-7-phosphaadamantane), DAPTA (3,7-diacetyl-1,3,7-triaza-5-phosphabicyclo[3.3.1]nonane)] with the in situ generated sodium salts of the heterocyclic thiones S-m-methylpyrimidine-2-thione, S-4,6-dimethylpyrimidine-2-thione, S-4,6-dihydroxypyrimidine-2-thione, benzothiazole-2-thione, benzoxazole-2-thione, S-1,3,4,-thiadiazole-2-thione, S-4,5-H-thiazolan-2-thione, and S-primidine-4(1H)-one-2-thione. The X-ray structures of six of the compounds confirm the trans disposition and, only in the case of [Pd2Cl2(S-pyrimidine-4(1H)-one-2-thionate)(2)(PTA)(2)], a dinuclear structure with a Pd-Pd distance of 3.0265(14)angstrom was observed. In vitro cytotoxicities against human ovarian cancer cell lines A2780 and A2780cisR were evaluated for ten complexes showing a high inhibition of cellular growth with a comparable inhibitory potency (IC50) against A2780 cells to that of cisplatin. Notably, the compounds also show significant (up to 7-fold higher) activity in cisplatin-resistant A2780cisR cell lines.
    DOI:
    10.1021/ic4006746
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