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Albumin-binding PARACEST agents

机译:结合白蛋白的PARACEST剂

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摘要

Lanthanide complexes (Eu3+, Gd3+ and Yb3+ of two different 1,4,7,10-tetraazacyclododecane-1,4,7,10-tetraacetic acid tetraamide derivatives containing two (2) and four (3) O-benzyl-L-serine amide substituents were synthesized and their chemical exchange saturation transfer (CEST) and relaxometric properties were examined in the presence and absence of human serum albumin (HSA). Both Eu2 and Eu3 display a significant CEST effect from a single slowly exchanging Eu3+-bound water molecule, making these PARACEST complexes potentially useful as vascular MRI agents. Yb2 also showed a detectable CEST effect from both the Yb3+-bound water protons and the exchangeable NH amide protons, making it potentially useful as a vascular pH sensor. Fluorescence displacement studies using reporter molecules indicate that both Gd2 and Gd3 displace dansylsarcosine from site II of HSA with inhibition constants of 32 and 96 mu M, respectively, but neither complex significantly displaces warfarin from site I. Water proton relaxation enhancements of 135 and 171% were observed upon binding of Gd2 and Gd3 to HSA, respectively, at 298 K and pH 7.4.
机译:镧系元素络合物(两种不同的1,4,7,10-四氮杂环十二烷-1,4,7,10-四乙酸四酰胺衍生物的Eu3 +,Gd3 +和Yb3 +,含有两(2)和四(3)个O-苄基-L-丝氨酸合成了酰胺取代基,并在有和没有人血清白蛋白(HSA)的情况下检查了它们的化学交换饱和转移(CEST)和弛豫特性,Eu2和Eu3均显示出一个缓慢交换的与Eu3 +结合的水分子的显着CEST效果。 ,使得这些PARACEST配合物潜在地可用作血管MRI剂,Yb2还显示了结合Yb3 +的水质子和可交换的NH酰胺质子均具有可检测到的CEST效应,使其潜在地可用作血管pH传感器。表明Gd2和Gd3都分别以32和96μM的抑制常数从HSA的位点II取代了Dansylsarcosine,但是这两种复合物都不能从位点I显着取代华法林。在298 K和pH 7.4下,分别将Gd2和Gd3与HSA结合后,观察到的质子弛豫增强为135%和171%。

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