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Gd(III)-1,4,7-tris(carboxymethyl)-2,2′,2″-(10-(2-oxo-2-((1-tetradecyl-1H-1,2,3-triazol-4-yl)methyl)-amino)ethyl)-1,4,7,10-tetraazacyclododecane | 1609385-09-2

中文名称
——
中文别名
——
英文名称
Gd(III)-1,4,7-tris(carboxymethyl)-2,2′,2″-(10-(2-oxo-2-((1-tetradecyl-1H-1,2,3-triazol-4-yl)methyl)-amino)ethyl)-1,4,7,10-tetraazacyclododecane
英文别名
——
Gd(III)-1,4,7-tris(carboxymethyl)-2,2′,2″-(10-(2-oxo-2-((1-tetradecyl-1H-1,2,3-triazol-4-yl)methyl)-amino)ethyl)-1,4,7,10-tetraazacyclododecane化学式
CAS
1609385-09-2
化学式
C33H57GdN8O7
mdl
——
分子量
835.115
InChiKey
IQEMFDZECLEEEN-UHFFFAOYSA-K
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:
    1-azidotetradecane1-{2-[(prop-2-ynyl)amino]-2-oxoethyl}-4,7,10- tris(carboxymethyl)-1,4,7,10-tetraazacyclododecyl gladolinium(III)copper(II) sulfatesodium ascorbate 作用下, 以 叔丁醇 为溶剂, 反应 48.0h, 以26%的产率得到Gd(III)-1,4,7-tris(carboxymethyl)-2,2′,2″-(10-(2-oxo-2-((1-tetradecyl-1H-1,2,3-triazol-4-yl)methyl)-amino)ethyl)-1,4,7,10-tetraazacyclododecane
    参考文献:
    名称:
    Cell Labeling via Membrane-Anchored Lipophilic MR Contrast Agents
    摘要:
    Cell tracking in vivo with MR imaging requires the development of contrast agents with increased sensitivity that effectively label and are retained by cells. Most clinically approved Gd(III)-based contrast agents require high incubation concentrations and prolonged incubation times for cellular internalization. Strategies to increase contrast agent permeability have included conjugating Gd(III) complexes to cell penetrating peptides, nanoparticles, and small molecules which have greatly improved cell labeling but have not resulted in improved cellular retention. To overcome these challenges, we have synthesized a series of lipophilic Gd(III)-based MR contrast agents that label cell membranes in vitro. Two of the agents were synthesized with a multiplexing strategy to contain three Gd(III) chelates (1 and 2) while the third contains a single Gd(III) chelate (3). These new agents exhibit significantly enhanced labeling and retention in HeLa and MDA-MB-231-mcherry cells compared to agents that are internalized by cells (4 and Prohance).
    DOI:
    10.1021/bc500083t
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