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cis-[Pt(NO3)2(5,7-di-tert-butyl-1,2,4-triazolo[1,5-a]pyrimidine)2] | 1403824-95-2

中文名称
——
中文别名
——
英文名称
cis-[Pt(NO3)2(5,7-di-tert-butyl-1,2,4-triazolo[1,5-a]pyrimidine)2]
英文别名
cis-[Pt(NO3)2(dbtp)2]
cis-[Pt(NO<sub>3</sub>)<sub>2</sub>(5,7-di-tert-butyl-1,2,4-triazolo[1,5-a]pyrimidine)<sub>2</sub>]化学式
CAS
1403824-95-2
化学式
C26H42N10O6Pt
mdl
——
分子量
785.763
InChiKey
JZLLHIMKXJGFTR-UHFFFAOYSA-N
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):
    None
  • 重原子数:
    None
  • 可旋转键数:
    None
  • 环数:
    None
  • sp3杂化的碳原子比例:
    None
  • 拓扑面积:
    None
  • 氢给体数:
    None
  • 氢受体数:
    None

反应信息

  • 作为产物:
    描述:
    cis-[PtI2(5,7-di-tert-butyl-1,2,4-triazolo[1,5-a]pyrimidine)2]silver nitrate丙酮 为溶剂, 反应 48.0h, 以93%的产率得到cis-[Pt(NO3)2(5,7-di-tert-butyl-1,2,4-triazolo[1,5-a]pyrimidine)2]
    参考文献:
    名称:
    Structure-cytotoxicity relationship for different types of mononuclear platinum(II) complexes with 5,7-ditertbutyl-1,2,4-triazolo[1,5-a]pyrimidine
    摘要:
    To compare the in vitro cytotoxicity of platinum(II) complexes with 5,7-ditertbutyl-1,2,4-triazolo[1,5-a]pyrimidine (dbtp), three complexes were prepared: cis-[PtI2(dbtp)(2)] (1). cis-[Pt(NO3)(2)(dbtP)(2)] (2) and cis-[Pt(C4H4O5)(dbtp)(2)] (3). The coordination compounds have been structurally characterized by IR; H-1, C-13, N-15, Pt-195 NMR and single-crystal X-ray diffraction (1). Spectroscopic studies reveal the monodentate coordination of the heterocycle ligand (dbtp) via N(3) to platinum(II) ions. In addition, the crystal structure of (1) shows that the platinum(II) ion is located in nearly square-planar PtI2N2 environments with two heterocycle ligands (dbtp) arranged in a head-to-head orientation. The complexes have been screened for their cytotoxicity against two human cells: non-small cell lung carcinoma (A549) and breast cancer (T47D). All of the complexes demonstrated a significant antiproliferative activity against both cell lines. On the basis of these results, it is concluded that the cytotoxicity of the studied compounds against T47D follows the order: (3) < (1) < (2). (C) 2012 Elsevier Inc. All rights reserved.
    DOI:
    10.1016/j.jinorgbio.2012.05.005
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