Development of a luminescence-controllable firefly luciferin analogue using selective enzymatic cyclization

Shuji Ioka, Tsuyoshi Saitoh, Shojiro A. Maki, Masaya Imoto, Shigeru Nishiyama

研究成果: Article査読

4 被引用数 (Scopus)

抄録

In this study, a new firefly luciferin analog that can switch firefly bioluminescence (BL) activity from ‘off’ to ‘on’ state was designed and synthesized. BL inactive N-Ac-γ-glutamate luciferin 3 contains an acyclic precursor of the thiazoline moiety. Enzymatic treatment of 3 with aminoacylase resulted in a smooth removal of the acyl protecting group and concomitant cyclization to provide BL active carboluciferin 2.

本文言語English
ページ(範囲)7505-7508
ページ数4
ジャーナルTetrahedron
72
47
DOI
出版ステータスPublished - 2016

ASJC Scopus subject areas

  • 生化学
  • 創薬
  • 有機化学

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