Issue 20, 1994
From the journal:

Journal of the Chemical Society, Chemical Communications

Synthesis and preliminary chemie- and bio-iuminescence studies of a novel photolabile coelenterazine analogue with a trifluoromethyl diazirine group

Feng-Qi Chen,   Takashi Hirano,   Yoshinobu Hashizume,   Yoshihiro Ohmiya  and  Mamoru Ohashi  

Abstract

A novel photolabile analogue of coelenterazine with a trifluoromethyl diazirine group is successfully synthesized for photoaffinity labelling of the active site of aequorin; preliminary studies on its chemi-and bio-luminescence demonstrate that the photolabile analogue shows the same luminescence properties and kinetics as those of natural coelenterazine and thus, it is deduced that both compounds occupy the same active site of aequorin.

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Article information

DOI
https://doi.org/10.1039/C39940002405
Article type
Paper

J. Chem. Soc., Chem. Commun., 1994, 2405-2406

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Synthesis and preliminary chemie- and bio-iuminescence studies of a novel photolabile coelenterazine analogue with a trifluoromethyl diazirine group

F. Chen, T. Hirano, Y. Hashizume, Y. Ohmiya and M. Ohashi, J. Chem. Soc., Chem. Commun., 1994, 2405 DOI: 10.1039/C39940002405

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