Peptide-based short single β-strand mimics without hydrogen bonding or aggregation
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- Luhan Zhai
- Laboratory of Organic and Medicinal Chemistry
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- Yuko Otani
- Laboratory of Organic and Medicinal Chemistry
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- Yukiko Hori
- Laboratory of Neuropathology & Neuroscience
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- Taisuke Tomita
- Laboratory of Neuropathology & Neuroscience
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- Tomohiko Ohwada
- Laboratory of Organic and Medicinal Chemistry
書誌事項
- 公開日
- 2020
- 資源種別
- journal article
- 権利情報
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- http://rsc.li/journals-terms-of-use
- DOI
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- 10.1039/c9cc08378b
- 公開者
- Royal Society of Chemistry (RSC)
この論文をさがす
説明
<p>Both (<italic>R</italic>- and <italic>S</italic>-) enantiomers of the bridgehead-substituted β-proline analogue (<italic>i.e.</italic>, 7-azabicyclo[2.2.1]heptane-2-carboxylic acid or Abh amino acid (<bold>Abh-AA</bold>)) can work as a new scaffold for single β-strand enforcement and propagation.</p>
収録刊行物
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- Chemical Communications
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Chemical Communications 56 (10), 1573-1576, 2020
Royal Society of Chemistry (RSC)