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含酰胺、醇或酮侧基的基于1,4,7-三氮杂环壬烷的螯合剂的[铼]铼和[锝]锝三羰基金属配合物

[Re]Re- and [Tc]Tc-Tricarbonyl Metal Complexes with 1,4,7-Triazacyclononane-Based Chelators Bearing Amide, Alcohol, or Ketone Pendent Groups.

作者信息

Hoerres Rebecca, Kamboj Ritin, Pryor Nora, Kelley Steven P, Hennkens Heather M

机构信息

Department of Chemistry, University of Missouri, 601 South College Avenue, Columbia, Missouri 65211, United States.

Research Reactor Center, University of Missouri, 1513 Research Park Drive, Columbia, Missouri 65211, United States.

出版信息

ACS Omega. 2024 Sep 11;9(38):39925-39935. doi: 10.1021/acsomega.4c05699. eCollection 2024 Sep 24.

Abstract

1,4,7-Triazacyclononane (TACN)-based chelators, such as NOTA and NODAGA, have shown great promise as bifunctional chelators for [M(CO)] cores (M = Tc and Re) in radiopharmaceutical development. Previous investigations of TACN-based chelators bearing pendent acid and ester arms demonstrated the important role the pendent arms have in successful coordination of the [M(CO)] core with the TACN backbone nitrogens. In this work, we introduce three TACN-based bifunctional chelators bearing amide, alcohol, and ketone pendent arms and evaluate their (radio)labeling efficiency with the [M(CO)] core as well as the stability and hydrophilicity of the resulting radiometal complexes. Following their synthesis and characterization, the amide () and alcohol () chelators were successfully labeled with the [M(CO)] cores (M = Re, Tc, and Re), while the ketone () was not successfully labeled. Radiometal complexes and demonstrated hydrophilic character in logD studies as well as excellent stability in phosphate-buffered saline (pH 7.4), l-histidine, l-cysteine, and rat serum at 37 °C through 24 h. While the hydrophilicity and stability of these radiocomplexes are attractive, future TACN chelator design modifications to increase radiolabeling yields under milder reaction conditions would improve their potential for use in development of [M(CO)] radiopharmaceuticals.

摘要

基于1,4,7-三氮杂环壬烷(TACN)的螯合剂,如NOTA和NODAGA,在放射性药物开发中作为用于[M(CO)]核(M = Tc和Re)的双功能螯合剂已显示出巨大潜力。先前对带有侧链酸和酯臂的基于TACN的螯合剂的研究表明,侧链臂在[M(CO)]核与TACN主链氮的成功配位中起着重要作用。在这项工作中,我们引入了三种带有酰胺、醇和酮侧链臂的基于TACN的双功能螯合剂,并评估了它们与[M(CO)]核的(放射性)标记效率以及所得放射性金属配合物的稳定性和亲水性。在合成和表征之后,酰胺()和醇()螯合剂成功地用[M(CO)]核(M = Re、Tc和Re)进行了标记,而酮()未成功标记。放射性金属配合物和在logD研究中表现出亲水性,并且在37°C下于磷酸盐缓冲盐水(pH 7.4)、l-组氨酸、l-半胱氨酸和大鼠血清中24小时内表现出优异的稳定性。虽然这些放射性配合物的亲水性和稳定性很有吸引力,但未来对TACN螯合剂设计进行修饰以在更温和的反应条件下提高放射性标记产率将改善它们在[M(CO)]放射性药物开发中的应用潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/af03/11425660/c647cb599894/ao4c05699_0004.jpg

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