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Synthesis of 4-[211At]astato-L-phenylalanine via electrophilic demetallation from a silyl precursor
https://repo.qst.go.jp/records/75572
https://repo.qst.go.jp/records/75572133e80dd-03ba-4aae-95b7-657ce9628669
Item type | 会議発表用資料 / Presentation(1) | |||||
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公開日 | 2019-03-13 | |||||
タイトル | ||||||
タイトル | Synthesis of 4-[211At]astato-L-phenylalanine via electrophilic demetallation from a silyl precursor | |||||
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 |
Watanabe, Shigeki
× Watanabe, Shigeki× Mohammad, Anwar-Ul Azim× Nishinaka, Ichiro× Sasaki, Ichiro× Oshima, Yasuhiro× Yamada, Keiichi× Ishioka, Noriko× Watanabe, Shigeki× Nishinaka, Ichiro× Sasaki, Ichiro× Oshima, Yasuhiro× Ishioka, Noriko |
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抄録 | ||||||
内容記述タイプ | Abstract | |||||
内容記述 | The astatine-211 (At-211) labeled compound, 4-[211At]astato-L-phenylalanine, is one of the most promising amino acid derivatives for use in targeted alpha therapy (TAT) for various cancers. Electrophilic demetallation of stannyl precursor is the most widely used approach for labeling biomolecules with At-211. However, the low acid-resistance of the stannyl precursor necessitates the use of a N- and C- terminus protected precursor, which causes low overall radiochemical yield (RCY) due to the multiple synthetic steps involved. A deprotected organosilyl compound, 4-triethylsilylphenylalanine, was employed for direct synthesis of the astatinated phenylalanine in this study. | |||||
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 | 11th International Symposium on Targeted-Alpha-Therapy (TAT11) | |||||
発表年月日 | ||||||
日付 | 2019-04-02 | |||||
日付タイプ | Issued |