1262117-93-0Relevant articles and documents
A novel coelenterate luciferin-based luminescent probe for selective and sensitive detection of thiophenols
Yuan, Mingliang,Ma, Xiaojie,Jiang, Tianyu,Zhang, Chaochao,Chen, Hui,Gao, Yuqi,Yang, Xingye,Du, Lupei,Li, Minyong
, p. 10267 - 10274 (2016)
The first dual bioluminescent and chemiluminescent sensor for detecting highly toxic thiophenols has been developed. Such a probe was designed by using a coelenterazine analogue as the luminophore and dinitrophenyl ether as the recognition moiety. It shou
Luminescence of coelenterazine derivatives with C-8 extended electronic conjugation
Yuan, Ming-Liang,Jiang, Tian-Yu,Du, Lu-Pei,Li, Min-Yong
, p. 550 - 554 (2016/04/26)
Replacement of the methylene group at the C-8 position with an extended electronic conjugation is a new promising method to develop red-shifted coelenterazine derivatives. In this paper, we have described an oxygen-containing coelenterazine derivative with a significant red-shifted (63 nm) bioluminescence signal maximum relative to coelenterazine 400a (DeepBlueC, 1). In cell imaging, the sulfur-containing coelenterazine derivative displayed a significantly (1.77 ± 0.09; P ≤ 0.01) higher luminescence signal compared to coelenterazine 400a and the oxygen-containing coelenterazine derivative exhibited a slightly (0.74 ± 0.08; P ≤ 0.05) lower luminescence signal. It is beneficial to understand further the underlying mechanisms of bioluminescence.
New red-shifted coelenterazine analogues with an extended electronic conjugation
Giuliani, Germano,Molinari, Paola,Ferretti, Giulia,Cappelli, Andrea,Anzini, Maurizio,Vomero, Salvatore,Costa, Tommaso
experimental part, p. 5114 - 5118 (2012/10/07)
A new promising approach to the development of red-shifted coelenterazine analogues was described. In order to alter the photochemical properties of native coelenterazine, we have designed and synthesized analogues bearing a new electron-rich structure. T
IMIDAZO[1,2-α]PYRAZIN-3(7H)-ONE DERIVATIVES BEARING A NEW ELECTRON-RICH STRUCTURE
-
Page/Page column 39-40, (2011/02/24)
The present invention relates to compound of formula I : and their use as chemiluminescent and/or bioluminescent reagents.