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  1. 原著論文

Discovery of Pyrazole-Based Positron Emission Tomography Agent that Maps Histone Deacetylase 6 (HDAC6) in the Nonhuman Primate Brain

https://repo.qst.go.jp/records/2001909
https://repo.qst.go.jp/records/2001909
2391b551-9ee9-4f39-b1da-6b66ab367c88
アイテムタイプ 学術雑誌論文 / Journal Article(1)
公開日 2025-10-27
タイトル
タイトル Discovery of Pyrazole-Based Positron Emission Tomography Agent that Maps Histone Deacetylase 6 (HDAC6) in the Nonhuman Primate Brain
言語 en
言語
言語 eng
資源タイプ
資源タイプ識別子 http://purl.org/coar/resource_type/c_6501
資源タイプ journal article
著者 Yamasaki Tomoteru

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Yamasaki Tomoteru

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Norio Ohyabu

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Norio Ohyabu

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Wakabayashi Takeshi

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Wakabayashi Takeshi

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Ignacio Ibáñez

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Ignacio Ibáñez

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Kouichi Iwanaga

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Kouichi Iwanaga

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Satoshi Yamamoto

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Satoshi Yamamoto

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Masahiko Hattori

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Masahiko Hattori

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Taku Sugita

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Taku Sugita

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Michiko Terada

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Michiko Terada

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Tomohiro Onishi

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Tomohiro Onishi

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Sho Sato

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Sho Sato

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Yohei Kosugi

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Yohei Kosugi

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Akihiro Takano

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Akihiro Takano

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Paul McQuade

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Paul McQuade

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Takamitsu Maru

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Takamitsu Maru

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Naomi Inui

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Naomi Inui

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Fujinaga Masayuki

× Fujinaga Masayuki

Fujinaga Masayuki

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Mori Wakana

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Mori Wakana

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Nagai Yuji

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Nagai Yuji

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Seki Chie

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Seki Chie

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Uchida Shoko

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Uchida Shoko

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Minamimoto Takafumi

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Minamimoto Takafumi

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Higuchi Makoto

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Higuchi Makoto

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Makoto Fushimi

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Makoto Fushimi

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Zhang Ming-Rong

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Zhang Ming-Rong

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抄録
内容記述タイプ Abstract
内容記述 Histone deacetylase 6 (HDAC6) is a crucial target for the development of pharmaceuticals used in the treatment of neurodegenerative disorders. Here, we identified 16a as a candidate of positron emission tomography (PET) tracer for HDAC6 imaging from pyrazole derivatives, which showed strong HDAC6 affinity (Kd = 1.66 nM) and higher accumulation in the brain of wild-type mice than in HDAC6 knockout mice. Following radiolabeling with fluorine-18, PET with [18F]16a exhibited heterogeneous uptake of radioactivity, corresponding to the biological distribution of HDAC6 in the monkey brain. These radioactive distributions were homogeneously diminished by the preadministration of ACY-775, a potent inhibitor of HDAC6, suggesting that radioactive accumulation in PET images could reflect the specific binding of [18F]16a with HDAC6. Thus, [18F]16a is a promising PET tracer for HDAC6 imaging that motivates future clinical research.
書誌情報 Journal of Medicinal Chemistry

発行日 2025-10
出版者
出版者 ACS Publications
ISSN
収録物識別子タイプ ISSN
収録物識別子 1520-4804
DOI
識別子タイプ DOI
関連識別子 10.1021/acs.jmedchem.5c02216
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Ver.1 2026-01-06 05:27:47.642501
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