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| 1187842-06-3

中文名称
——
中文别名
——
英文名称
——
英文别名
——
化学式
CAS
1187842-06-3
化学式
C36H24N8O4S4
mdl
——
分子量
760.902
InChiKey
QQPNDLZCSUVOPA-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):
    6.67
  • 重原子数:
    52.0
  • 可旋转键数:
    0.0
  • 环数:
    9.0
  • sp3杂化的碳原子比例:
    0.11
  • 拓扑面积:
    139.56
  • 氢给体数:
    0.0
  • 氢受体数:
    16.0

反应信息

  • 作为产物:
    描述:
    1,2-二溴乙烷S,S'-bis(2-benzimidazolyl)1,2-dithiooxalatepotassium carbonate 、 potassium iodide 作用下, 以 乙腈 为溶剂, 反应 7.0h, 以71%的产率得到
    参考文献:
    名称:
    Interaction studies of a novel Co(II)-based potential chemotherapeutic agent with human serum albumin (HSA) employing biophysical techniques
    摘要:
    Novel macrocyclic cobalt(II) complex C36H24N8O4S4CoCl2 with a butterfly topology was synthesized and characterized by spectroscopic (IR, H-1, C-13 NMR, EPR, UV-Vis, ESI-MS) and analytical methods. The complex exhibits distorted octahedral geometry around Co(II) metal ion, which was confirmed by EPR measurements with g(a), g(b), and g(c) values (8.01, 2.20, and 1.66), respectively, and molar extinction coefficient epsilon = 58 M(-1)cm(-1). The Interaction studies with human serum albumin (HSA) in phosphate buffer (0.1 M, pH 7.0) were studied by electronic absorption titration, fluorescence titration, circular dichroism, and cyclic voltammetry. Hyperchromism in fluorescence intensity indicates binding of complex with HSA near tryptophan residue in IIA subdomain leading to less polar microenvironment around tryptophan and more at tyrosine. The intrinsic binding constant K (b) obtained from absorption spectral titrations was found to be 9.3 x 10(4) M-1, suggesting medium binding affinity of HSA with complex. CD spectrum indicates alpha-helical structure up to beta-pleated secondary structure. CV data confirmed medium reversible binding with HSA. The binding of complex with HSA shows typical reversible mode of binding, which enables the delivery of drug candidate to the tissue enzymes and receptors in an efficient manner, and thereby affects the uptake of the drug.
    DOI:
    10.1007/s00044-009-9231-7
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