Discovery of <sup>18</sup>F Labeled AZD5213 Derivatives as Novel Positron Emission Tomography (PET) Radioligands Targeting Histamine Subtype‐3 Receptor

The histamine subtype 3 (H<sub>3</sub>) receptor is an important drug target in the central nervous system (CNS), and PET imaging offers a promising technique for the noninvasive evaluation of CNS disease related to the H<sub>3</sub> receptor. In this study, we synthesized and evaluated the binding effects of [<sup>18</sup>F]H3-2404 and [<sup>18</sup>F]H3-2405 by modifying the structure of AZD5213, a selective H<sub>3</sub> antagonist. These two radioligands were prepared in high radiochemical yields and displayed stability in serum. The in vitro autoradiographic study in rat brain tissue and the following in vivo PET studies in mice demonstrated sufficient brain uptake but predominantly non-specific distribution in rodent brain. Although these data suggest that [<sup>18</sup>F]H3-2404 and [<sup>18</sup>F]H3-2405 are unsuitable as PET tracers for brain imaging of the H<sub>3</sub> receptor, this study provides a valuable attempt for optimizing <sup>18</sup>F labeled radiotracers based on AZD5213.

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Publication Details

Journal
ChemBioChem
Published
2024-09-20
DOI
https://doi.org/10.1002/cbic.202400655
Citations
3
Primary Topic
Mast cells and histamine
Type
article
Field-Weighted Citation Impact
0.72

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article

Discovery of 18F Labeled AZD5213 Derivatives as Novel Positron Emission Tomography (PET) Radioligands Targeting Histamine Subtype‐3 Receptor

Ahmed Haider, Linqi Zhang, Zhendong Song, Steven H. Liang et al.
3 citations
ChemBioChem
Mast cells and histamine
0.72
article

Discovery of 18F Labeled AZD5213 Derivatives as Novel Positron Emission Tomography (PET) Radioligands Targeting Histamine Subtype‐3 Receptor

Ahmed Haider, Linqi Zhang, Zhendong Song, Steven H. Liang, Kenneth Dahl, Chongzhao Ran, Chunyu Zhao, Charles S. Elmore, Xin Mu Zhou, Yinlong Li, Magnus Schou, Chuangyan Zhai, Zhenkun Sun, Kim S. Mühlfenzl, Hongjie Yuan, Jiahui Chen, Jian Rong, Jimmy S. Patel, Yabiao Gao, Ahmad Chaudhary, Lee Collier
article en
3 citations

Abstract

The histamine subtype 3 (H<sub>3</sub>) receptor is an important drug target in the central nervous system (CNS), and PET imaging offers a promising technique for the noninvasive evaluation of CNS disease related to the H<sub>3</sub> receptor. In this study, we synthesized and evaluated the binding effects of [<sup>18</sup>F]H3-2404 and [<sup>18</sup>F]H3-2405 by modifying the structure of AZD5213, a selective H<sub>3</sub> antagonist. These two radioligands were prepared in high radiochemical yields and displayed stability in serum. The in vitro autoradiographic study in rat brain tissue and the following in vivo PET studies in mice demonstrated sufficient brain uptake but predominantly non-specific distribution in rodent brain. Although these data suggest that [<sup>18</sup>F]H3-2404 and [<sup>18</sup>F]H3-2405 are unsuitable as PET tracers for brain imaging of the H<sub>3</sub> receptor, this study provides a valuable attempt for optimizing <sup>18</sup>F labeled radiotracers based on AZD5213.

ChemBioChemVol. 26(5)
Harvard University (US), Emory University (US), Stockholm County Council (SE), Karolinska Institutet (SE), Massachusetts General Hospital (US), AstraZeneca (Netherlands) (NL), Athinoula A. Martinos Center for Biomedical Imaging (US), AstraZeneca (Sweden) (SE)
AstraZeneca, Emory University, School of Medicine, Emory University, National Cancer Institute
Good health and well-being
Openalex Percentile: Top 29%
Mast cells and histamine
0.72
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