SYNTHESIS AND PRELIMINARY CHEMILUMINESCENCE AND BIOLUMINESCENCE STUDIES OF A NOVEL PHOTOLABILE COELENTERAZINE ANALOG WITH A TRIFLUOROMETHYLDIAZIRINE GROUP
Fq. Chen et al., SYNTHESIS AND PRELIMINARY CHEMILUMINESCENCE AND BIOLUMINESCENCE STUDIES OF A NOVEL PHOTOLABILE COELENTERAZINE ANALOG WITH A TRIFLUOROMETHYLDIAZIRINE GROUP, Journal of the Chemical Society, Chemical Communications, (20), 1994, pp. 2405-2406
A novel photolabile analogue of coelenterazine with a trifluoromethyl
diazirine group is successfully synthesized for photoaffinity labellin
g of the active site of aequorin; preliminary studies on its chemi- an
d bio-luminescence demonstrate that the photolabile analogue shows the
same luminescence properties and kinetics as those of natural coelent
erazine and thus, it is deduced that both compounds occupy the same ac
tive site; of aequorin.