Synthesis and evaluation of a novel bifunctional ligand 3o-C-NETA for Yttrium-90 and Lutetium-177

IF 2.2 4区 医学 Q3 CHEMISTRY, MEDICINAL Bioorganic & Medicinal Chemistry Letters Pub Date : 2025-05-01 Epub Date: 2025-02-11 DOI:10.1016/j.bmcl.2025.130136
Hua Xu, Pengfei Dong, Haixing Wang, Inseok Sin, Chi Soo Kang, Siyuan Ren, Xiang Sun, Hyun-Soon Chong
{"title":"Synthesis and evaluation of a novel bifunctional ligand 3o-C-NETA for Yttrium-90 and Lutetium-177","authors":"Hua Xu,&nbsp;Pengfei Dong,&nbsp;Haixing Wang,&nbsp;Inseok Sin,&nbsp;Chi Soo Kang,&nbsp;Siyuan Ren,&nbsp;Xiang Sun,&nbsp;Hyun-Soon Chong","doi":"10.1016/j.bmcl.2025.130136","DOIUrl":null,"url":null,"abstract":"<div><div>A bifunctional ligand is an essential component for targeted cancer therapy using cytotoxic radionuclides. We report the synthesis and evaluation of a novel bifunctional ligand, 3o-<em>C</em>-NETA, designed for labeling a bioactive small molecule or an antibody with β-particle emitting radionuclides <sup>90</sup>Y and <sup>177</sup>Lu. 3o-<em>C</em>-NETA is an octadentate chelating agent and contains both a macrocyclic backbone (1,4,7-triazacyclononane, TACN) and pendant donor groups. 3o-<em>C</em>-NETA was efficiently synthesized via the regiospecific ring opening of a functionalized aziridinium ion with <em>tert</em>-Butyl protected NODA (1,4,7-triazacyclononane-1,4-diacetic acid) and evaluated for radiolabeling kinetics and <em>in vitro</em> complex stability with <sup>90</sup>Y and <sup>177</sup>Lu. The new bifunctional ligand (3o-<em>C</em>-NETA) rapidly bound to <sup>90</sup>Y or <sup>177</sup>Lu, and the corresponding <sup>90</sup>Y- or <sup>177</sup>Lu-labeled 3o-<em>C</em>-NETA remained stable in human serum for two weeks.</div></div>","PeriodicalId":256,"journal":{"name":"Bioorganic & Medicinal Chemistry Letters","volume":"120 ","pages":"Article 130136"},"PeriodicalIF":2.2000,"publicationDate":"2025-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Bioorganic & Medicinal Chemistry Letters","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0960894X25000459","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/2/11 0:00:00","PubModel":"Epub","JCR":"Q3","JCRName":"CHEMISTRY, MEDICINAL","Score":null,"Total":0}
引用次数: 0

Abstract

A bifunctional ligand is an essential component for targeted cancer therapy using cytotoxic radionuclides. We report the synthesis and evaluation of a novel bifunctional ligand, 3o-C-NETA, designed for labeling a bioactive small molecule or an antibody with β-particle emitting radionuclides 90Y and 177Lu. 3o-C-NETA is an octadentate chelating agent and contains both a macrocyclic backbone (1,4,7-triazacyclononane, TACN) and pendant donor groups. 3o-C-NETA was efficiently synthesized via the regiospecific ring opening of a functionalized aziridinium ion with tert-Butyl protected NODA (1,4,7-triazacyclononane-1,4-diacetic acid) and evaluated for radiolabeling kinetics and in vitro complex stability with 90Y and 177Lu. The new bifunctional ligand (3o-C-NETA) rapidly bound to 90Y or 177Lu, and the corresponding 90Y- or 177Lu-labeled 3o-C-NETA remained stable in human serum for two weeks.

Abstract Image

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
新型钇-90和镥-177双功能配体30 - c - neta的合成与评价。
双功能配体是使用细胞毒性放射性核素靶向癌症治疗的重要组成部分。我们报道了一种新的双功能配体30 - c - neta的合成和评价,该配体设计用于标记具有生物活性的小分子或具有发射放射性核素90Y和177Lu的β-颗粒的抗体。30 - c - neta是一种十八齿酸螯合剂,含有大环主链(1,4,7-三氮杂环壬烷,TACN)和垂链供体基团。用叔丁基保护的NODA(1,4,7-三氮环壬烷-1,4-二乙酸)通过功能化氮铱离子的区域特异性开环高效合成了30 - c - neta,并对其与90Y和177Lu的放射性标记动力学和体外配合物稳定性进行了评价。新的双功能配体(30 - c - neta)快速结合90Y或177Lu,相应的90Y或177Lu标记的30 - c - neta在人血清中保持稳定两周。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
CiteScore
5.70
自引率
3.70%
发文量
463
审稿时长
27 days
期刊介绍: Bioorganic & Medicinal Chemistry Letters presents preliminary experimental or theoretical research results of outstanding significance and timeliness on all aspects of science at the interface of chemistry and biology and on major advances in drug design and development. The journal publishes articles in the form of communications reporting experimental or theoretical results of special interest, and strives to provide maximum dissemination to a large, international audience.
期刊最新文献
Discovery of imidazole-based apo-IDO1 inhibitors: rational design, synthesis, and biological evaluation Synthesis of novel 5,6,6a,8-tetrahydro-1H-benzo[5,6]oxepino[2,3,4-de]quinoline fused iminosugars as uncompetitive inhibitors against α-glucosidase Synthesis of mitochondria-targeted podophyllotoxin derivatives for the imaging and antiproliferation of liver cancer Virucidal multipurpose aqueous solution containing quaternary ammonium cation and sulfobetaine is effective against highly pathogenic avian influenza viruses Discovery of tetrahydroisoquinoline derivatives as selective histone deacetylase 6 inhibitors with neurite outgrowth-promoting activities and neuroprotective activities
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1