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[Ga(N,N′-[1-benzyl-1,2,3-triazole-4-yl]methyl-N,N′-[6-(carboxy)-pyridin-2-yl]-1,2-diaminoethane(-2H))](ClO4) | 1404288-27-2

中文名称
——
中文别名
——
英文名称
[Ga(N,N′-[1-benzyl-1,2,3-triazole-4-yl]methyl-N,N′-[6-(carboxy)-pyridin-2-yl]-1,2-diaminoethane(-2H))](ClO4)
英文别名
[Ga(azapa)](ClO4)
[Ga(N,N′-[1-benzyl-1,2,3-triazole-4-yl]methyl-N,N′-[6-(carboxy)-pyridin-2-yl]-1,2-diaminoethane(-2H))](ClO<sub>4</sub>)化学式
CAS
1404288-27-2
化学式
C36H34GaN10O4*ClO4
mdl
——
分子量
839.904
InChiKey
WXDGKNQOXJHBBC-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

反应信息

  • 作为产物:
    描述:
    gallium(III) perchlorate hexahydrate 、 N,N′-[1-benzyl-1,2,3-triazole-4-yl]methyl-N,N′-[6-(carboxy)-pyridin-2-yl]-1,2-diaminoethane dihydrochloride 在 盐酸 、 sodium hydroxide 作用下, 以 为溶剂, 反应 24.0h, 生成 [Ga(N,N′-[1-benzyl-1,2,3-triazole-4-yl]methyl-N,N′-[6-(carboxy)-pyridin-2-yl]-1,2-diaminoethane(-2H))](ClO4)
    参考文献:
    名称:
    H2azapa: a Versatile Acyclic Multifunctional Chelator for 67Ga, 64Cu, 111In, and 177Lu
    摘要:
    Preliminary experiments with the novel acyclic triazole-containing bifunctional chelator H(2)azapa and the radiometals Cu-64, Ga-67, In-111, and Lu-177 have established its significant versatile potential as an alternative to 1,4,7,10-tetraazacyclododecane-1,4,7,10-tetraacetic acid (DOTA) for metal-based radiopharmaceuticals. Unlike DOTA, H(2)azapa radiolabels quantitatively with Cu-64, Ga-67, In-111, and Lu-177 in 10 min at room temperature. In vitro competition experiments with human blood serum show that Cu-64 remained predominantly chelate-bound, with only 2% transchelated to serum proteins after 20 h. Biodistribution experiments with [Cu-64(azapa)] in mice reveal uptake in various organs, particularly in the liver, lungs, heart, intestines, and kidneys. When compared to [Cu-64(DOTA)](2-), the lipophilic neutral [Cu-64(azapa)] was cleared through the gastrointestinal tract and accumulated in the liver, which is common for lipophilic compounds or free Cu-64. The chelator H(2)azapa is a. model complex for a click-based bifunctional chelating agent, and the lipophilic benzyl "place-holders" will be replaced by hydrophilic peptides to modulate the pharmacokinetics and direct activity away from the liver and gut. The solid-state molecular structure of [In(azapa)(H2O)][ClO4] reveals a very rare eight-coordinate distorted square antiprismatic geometry with one triazole arm bound, and the structure of [Cu-64(azapa)] shows a distorted octahedral geometry. The present study demonstrates significant potential for bioconjugates of H(2)azapa as alternatives to DOTA in copper based radiopharmaceuticals, with the highly modular and "clickable" molecular scaffold of H(2)azapa easily modified into a variety of bioconjugates. H(2)azapa is a versatile addition to the "pa" family, joining the previously published H(2)dedpa (Ga-67/68 and Cu-64), H(4)octapa (In-111, Lu-177, and Y-90), and H(5)decapa (Ac-225) to cover a wide range of important nuclides.
    DOI:
    10.1021/ic302225z
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