Incorporation of Fluorine into an OBOC Peptide Library by Copper-Free Click Chemistry toward the Discovery of PET Imaging Agents

被引:6
|
作者
Murrell, Emily [1 ]
Luyt, Leonard G. [1 ,2 ,3 ,4 ]
机构
[1] Univ Western Ontario, Dept Chem, London, ON N6A 5B7, Canada
[2] Univ Western Ontario, Dept Oncol, London, ON N6A 5B7, Canada
[3] Univ Western Ontario, Dept Med Imaging, London, ON N6A 5B7, Canada
[4] Lawson Hlth Res Inst, London Reg Canc Program, London, ON N6A 4L6, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
OBOC; fluorine-18; click chemistry; molecular imaging; CXCR4; HIGH-AFFINITY; COMBINATORIAL CHEMISTRY; CXCR4; INTEGRIN; RECEPTOR; EXPRESSION; LIGANDS;
D O I
10.1021/acscombsci.9b00146
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
A one-bead one-compound (OBOC) library of peptide-based imaging agents was developed where a F-19-containing moiety was added onto the N-terminus of octamer peptides through copper-free click chemistry prior to screening of the library. This created a library of complete imaging agents that was screened against CXCR4, a receptor of interest for cancer imaging. The screen directly resulted in the discovery of a peptide-based imaging agent with an IC50 of 138 mu M. This proof-of-concept study describes a new type of OBOC peptide library design, where hits discovered from screening can be easily translated into their fluorine-18 counterpart for PET imaging without loss of affinity.
引用
收藏
页码:109 / 113
页数:5
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