Literature DB >> 26403487

Synthetic Routes to Coelenterazine and Other Imidazo[1,2-a]pyrazin-3-one Luciferins: Essential Tools for Bioluminescence-Based Investigations.

Eloi P Coutant1,2, Yves L Janin3,4.   

Abstract

In the last few decades, bioluminescent systems based on the expression of a luciferase and the addition of a luciferin to monitor the emission of light have become very important tools for biological investigations. A growing proportion of these systems use coelenterazine or analogues of imidazo[1,2-a]pyrazine luciferins along with photoproteins or luciferases from sea creatures such as Aequorea, Renilla, Gaussia or Oplophorus. Central to the success of these tools are the synthetic pathways developed not only to prepare the naturally occurring luciferins, but also to design altered compounds that exhibit improved bioluminescence. Current work is indeed focused on the design of systems exhibiting extended luminescence ("glow" systems) or redshifted wavelengths, as well as constructions better adapted to conditions in cells or in vivo. This review describes the synthetic pathways used to prepare imidazo[1,2-a]pyrazine luciferins along with the research efforts aimed at preparing analogues even better suited to the design of assays.
© 2015 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Entities:  

Keywords:  heterocycles; luciferins; luminescence; natural products; photoproteins

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Year:  2015        PMID: 26403487     DOI: 10.1002/chem.201501531

Source DB:  PubMed          Journal:  Chemistry        ISSN: 0947-6539            Impact factor:   5.236


  3 in total

1.  Synthetic Coelenterazine Derivatives and Their Application for Bioluminescence Imaging.

Authors:  Tianyu Jiang; Minyong Li
Journal:  Methods Mol Biol       Date:  2022

2.  Synthesis of unnatural α-amino esters using ethyl nitroacetate and condensation or cycloaddition reactions.

Authors:  Glwadys Gagnot; Vincent Hervin; Eloi P Coutant; Sarah Desmons; Racha Baatallah; Victor Monnot; Yves L Janin
Journal:  Beilstein J Org Chem       Date:  2018-11-15       Impact factor: 2.883

3.  Unnatural α-amino ethyl esters from diethyl malonate or ethyl β-bromo-α-hydroxyiminocarboxylate.

Authors:  Eloi P Coutant; Vincent Hervin; Glwadys Gagnot; Candice Ford; Racha Baatallah; Yves L Janin
Journal:  Beilstein J Org Chem       Date:  2018-11-16       Impact factor: 2.883

  3 in total

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