首页> 外文期刊>Bioorganic and Medicinal Chemistry >Synthesis of a novel 'smart' bifunctional chelating agent 1-(2-[β,D-galactopyranosyloxy]ethyl)-7-(1-carboxy-3-[4-aminopheny1]propyl)-4,10-bis(carboxymethyl)-1,4,7,10-tetraazacyclododecane (Gal-PA-DO3A-NH_2) and its Gd(III) complex
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Synthesis of a novel 'smart' bifunctional chelating agent 1-(2-[β,D-galactopyranosyloxy]ethyl)-7-(1-carboxy-3-[4-aminopheny1]propyl)-4,10-bis(carboxymethyl)-1,4,7,10-tetraazacyclododecane (Gal-PA-DO3A-NH_2) and its Gd(III) complex

机译:新型“智能”双功能螯合剂1-(2- [β,D-吡喃半乳糖基氧基]乙基)-7-(1-羧基-3- [4-氨基苯基]丙基)-4,10-双(羧甲基)的合成-1,4,7,10-四氮杂环十二烷(Gal-PA-DO3A-NH_2)及其Gd(III)络合物

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摘要

A new synthetic pathway to 1-(2-[β,D-galactopyranosyloxy]ethyl)-7-(1-carboxy-3-[4-aminophenyl]propyl)-4,10-bis(carboxymethyl)-1,4,7,10-tetraazacyclododecane (Gal-PA-DO3A-NH_2) and 1-(2-[β,D-galactopyranosyloxy]ethyl)-4,7,10-tris(carboxymethyl)-1, 4,7,10-tetraazacyclododecane (Gal-DO3A) chelating agents was developed involving full hydroxyl- and carboxyl- group protection in precursors to product. Two sequences of cyclen-N-functionalisation were subsequently investigated, one successfully, towards synthesis of the novel 'smart' bifunctional Gal-PA-DO3A-NH_2 chelate. The longitudinal proton relaxivities of the neutral [Gd-(Gal-PA-DO3A-NH_2)] and [Gd-(Gal-DO3A)] complexes were increased by 28% and 37% in the presence of β-galactosidase, respectively.
机译:1-(2- [β,D-吡喃半乳糖基氧基]乙基)-7-(1-羧基-3- [4-氨基苯基]丙基)-4,10-双(羧甲基)-1,4的新合成途径7,10-四氮杂环十二烷(Gal-PA-DO3A-NH_2)和1-(2- [β,D-吡喃半乳糖基氧基]乙基)-4,7,10-三(羧甲基)-1,4,7,10-四氮杂环十二烷(Gal-DO3A)螯合剂的开发涉及在产品前体中全面保护羟基和羧基。随后研究了两个环素-N-官能化序列,其中一个成功地用于合成新型“智能”双功能Gal-PA-DO3A-NH_2螯合物。在存在β-半乳糖苷酶的情况下,中性[Gd-(Gal-PA-DO3A-NH_2)]和[Gd-(Gal-DO3A)]复合物的纵向质子弛豫率分别提高了28%和37%。

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