WEKO3
アイテム
Design, Synthesis, and Evaluation of 11C-Labeled 3-Acetyl-indole Derivatives as Novel Positron-Emission Tomography Imaging Agent for Diacylglycerol Kinase Gamma (DGKγ) in Brain
https://repo.qst.go.jp/records/84101
https://repo.qst.go.jp/records/84101980d06cd-4490-4d24-8427-ac0c878c94ed
Item type | 会議発表用資料 / Presentation(1) | |||||
---|---|---|---|---|---|---|
公開日 | 2021-08-13 | |||||
タイトル | ||||||
タイトル | Design, Synthesis, and Evaluation of 11C-Labeled 3-Acetyl-indole Derivatives as Novel Positron-Emission Tomography Imaging Agent for Diacylglycerol Kinase Gamma (DGKγ) in Brain | |||||
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_c94f | |||||
資源タイプ | conference object | |||||
アクセス権 | ||||||
アクセス権 | metadata only access | |||||
アクセス権URI | http://purl.org/coar/access_right/c_14cb | |||||
著者 |
Hattori, Yasushi
× Hattori, Yasushi× Tomoteru, Yamasaki× Ohashi, Tomohiro× Miyanohana, Yuhei× Kusumoto, Tomokazu× Maeda, Ryouta× Miyamoto, Maki× Debori, Yasuyuki× Hata, Akiko× Zhang, Yiding× Hidekatsu, Wakizaka× Takeshi, Wakabayashi× Masayuki, Fujinaga× Yamashita, Ryo× Zhang, Ming-Rong× Koike, Tatsuki× Hattori, Yasushi× Tomoteru, Yamasaki× Zhang, Yiding× Hidekatsu, Wakizaka× Takeshi, Wakabayashi× Masayuki, Fujinaga× Zhang, Ming-Rong |
|||||
抄録 | ||||||
内容記述タイプ | Abstract | |||||
内容記述 | Diacylglycerol kinase gamma (DGKγ) is a subtype of DGK enzyme which catalyzes ATP-dependent conversion of diacylglycerol to phosphatidic acid. DGKγ, localized in brain, plays some important role in central nervous system. However, its function has not been widely investigated. Positron emission tomography (PET) imaging of DGKγ validates target engagement of therapeutic DGKγ inhibitors and investigates DGKγ levels under normal and disease conditions. In this study, we designed and synthesized a series of 3-acetyl indole derivatives as candidates for PET imaging agents for DGKγ. Among the synthesized compounds, 2- ((3-acetyl-1-(6-methoxypyridin-3-yl)-2-methyl-1H-indol-5-yl)oxy)-N-methylacetamide (9) exhibited potent inhibitory activity (IC50 = 30 nM) against DGKγ and desirable physicochemical properties allowing efficient blood-brain barrier penetration and low levels of undesirable non-specific binding. The radio-labeling of 9 followed by PET imaging of wild-type and DGKγ-deficient mice and rats indicated that [11C]9 ([11C]T-278) specifically binds to DGKγ and yields a high signal-noise ratio for DGKγ in rodent brains. |
|||||
会議概要(会議名, 開催地, 会期, 主催者等) | ||||||
内容記述タイプ | Other | |||||
内容記述 | AIMECS 2021 | |||||
発表年月日 | ||||||
日付 | 2021-11-29 | |||||
日付タイプ | Issued |