摩熵化学
数据库官网
小程序
打开微信扫一扫
首页 分子通 化学资讯 化学百科 反应查询 关于我们
请输入关键词

cis-PtCl2(4-(2-aminoethyl)aminomethyl-2-phenylquinoline) | 212001-34-8

中文名称
——
中文别名
——
英文名称
cis-PtCl2(4-(2-aminoethyl)aminomethyl-2-phenylquinoline)
英文别名
——
cis-PtCl2(4-(2-aminoethyl)aminomethyl-2-phenylquinoline)化学式
CAS
212001-34-8
化学式
C18H19Cl2N3Pt
mdl
——
分子量
543.355
InChiKey
VICUKXJPFYKAOJ-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

反应信息

  • 作为产物:
    描述:
    potassium tetrachloroplatinate(II) 、 4-(2-aminoethyl)aminomethyl-2-phenylquinoline trihydrochloride 在 KOH 作用下, 以 为溶剂, 以21%的产率得到cis-PtCl2(4-(2-aminoethyl)aminomethyl-2-phenylquinoline)
    参考文献:
    名称:
    Intercalator-linked cisplatin: synthesis and antitumor activity of cis-dichloroplatinum(II) complexes connected to acridine and phenylquinolines by one methylene chain
    摘要:
    Three novel intercalator-linked cisplatin-type platinum complexes, cis-[PtCl2(9-(2-aminoethyl)aminomethylacridine)] (1), cis-[PtCl2(4-(2-aminoethyl) aminomethyl-2-phenylquinoline)] (2), and cis-[PtCl2(8-(2-aminoethyl)aminomethyl-2-phenylquinoline)] (3) were synthesized, The structure of 1 was determined by X-ray crystallography (triclinic, space group P (1) over bar with a=15.007(6), b=15.597(4), c = 10.398(3) Angstrom, alpha=98.51(3)degrees, beta=96.79(3)degrees, gamma = 114.61(2)degrees, Z=4, R = 0.053, R-w=0.063). The antitumor activity of the platinum complexes was investigated against the HeLa cell. Compound 3 was the most cytotoxic among the complexes synthesized here and was more effective than cisplatin. It was suggested from microscopic analysis that the acridine complex 1, which had no cytotoxicity against the HeLa cell, was not incorporated in the nucleus of the cell. Against the P388 cell, however, complex 1 gave a more therapeutic result than 3. The covalent binding ability of the cisplatin moiety was suppressed significantly in these compounds. The results of molecular mechanics showed that intercalation and covalent binding could be compatible. The cytotoxicity and DNA binding ability of phenylquinoline-type ligands were also studied to evaluate the intrinsic cytotoxicity of the intercalator. From the duplex DNA denaturation experiment and fluorescent ethidium displacement assay, the DNA binding affinities of the ligands are in agreement with the cytotoxicity of these compounds and the corresponding platinum complexes. (C) 1998 Elsevier Science S.A. All rights reserved.
    DOI:
    10.1016/s0020-1693(98)00035-8
点击查看最新优质反应信息