TY - JOUR
T1 - キノンメチドを利用したケミカルバイオロジ
AU - Yoritate, Makoto
N1 - Publisher Copyright:
© 2020 Society of Synthetic Organic Chemistry. All rights reserved.
PY - 2020/7/1
Y1 - 2020/7/1
N2 - Quinonemethides (QM) are reactive chemical species which can be generated from o- and p-hydroxy benzyl alcohol derivatives even in aqueous media. Its unique reactivity is frequently utilized in organic synthesis and chemical biology. The high electrophilicity of QM would result in the rapid formation of a covalent bond with nucleophilic amino-acid residues in peptide or nucleic-acid bases. In addition, released leaving groups in the formation of QM can be designed as, for example, bioactive molecules for drug-delivery system and fluorophores for activity-based probe. Herein, recent reports associated with the quinonemethide chemistry are described.
AB - Quinonemethides (QM) are reactive chemical species which can be generated from o- and p-hydroxy benzyl alcohol derivatives even in aqueous media. Its unique reactivity is frequently utilized in organic synthesis and chemical biology. The high electrophilicity of QM would result in the rapid formation of a covalent bond with nucleophilic amino-acid residues in peptide or nucleic-acid bases. In addition, released leaving groups in the formation of QM can be designed as, for example, bioactive molecules for drug-delivery system and fluorophores for activity-based probe. Herein, recent reports associated with the quinonemethide chemistry are described.
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U2 - 10.5059/yukigoseikyokaishi.78.728
DO - 10.5059/yukigoseikyokaishi.78.728
M3 - 学術誌
AN - SCOPUS:85088558744
SN - 0037-9980
VL - 78
SP - 728
EP - 729
JO - Yuki Gosei Kagaku Kyokaishi/Journal of Synthetic Organic Chemistry
JF - Yuki Gosei Kagaku Kyokaishi/Journal of Synthetic Organic Chemistry
IS - 7
ER -