Literature DB >> 34549229

Novel furimazine derivatives for nanoluciferase bioluminescence with various C-6 and C-8 substituents.

Jie Li1, Xiaoxu Wang1, Gaopan Dong1, Chongzheng Yan1, Yuanyuan Cui1, Zheng Zhang1, Lupei Du1, Minyong Li1.   

Abstract

Nanoluciferase (NLuc) is the emerging commercially available luciferase considering its small size and superior bioluminescence performance. Nevertheless, this bioluminescence system has some limitations, including narrow emission wavelength and single substrate. Herein, a series of novel furimazine derivatives at the C-6 and C-8 positions of the imidazopyrazinone core have been designed and synthesized for extension of the bioluminescence substrates. It should be noted that two compounds, molecules A2 (2-(furan-2-ylmethyl)-6-(4-(hydroxymethyl)phenyl)-8-(phenylthio)imidazo[1,2-a]pyrazin-3(7H)-one) and A3 (2-(furan-2-ylmethyl)-6-(4-amino-3-fluorophenyl)-8-(phenylthio)imidazo[1,2-a]pyrazin-3(7H)-one), display reasonable bioluminescence properties for in vitro and in vivo biological evaluations. In particular, compound A3 can broaden the application of NLuc bioluminescence techniques, especially for in vivo bioluminescent imaging.

Entities:  

Year:  2021        PMID: 34549229     DOI: 10.1039/d1ob01098k

Source DB:  PubMed          Journal:  Org Biomol Chem        ISSN: 1477-0520            Impact factor:   3.876


  2 in total

Review 1.  Brightening up Biology: Advances in Luciferase Systems for in Vivo Imaging.

Authors:  Shirley Liu; Yichi Su; Michael Z Lin; John A Ronald
Journal:  ACS Chem Biol       Date:  2021-11-15       Impact factor: 5.100

2.  Comparative Investigation of the Chemiluminescent Properties of a Dibrominated Coelenterazine Analog.

Authors:  João Sousa; Carla M Magalhães; Patricia González-Berdullas; Joaquim C G Esteves da Silva; Luís Pinto da Silva
Journal:  Int J Mol Sci       Date:  2022-07-30       Impact factor: 6.208

  2 in total

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