Results 171 to 180 of about 7,015 (221)
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Journal of Photochemistry and Photobiology B: Biology, 2019
Imidazopyrazinone is a typical scaffold present in marine bioluminescence, in which thermal energy is converted into excitation energy in an enzyme-catalyzed reaction.
Carla M MAGALHÃES +2 more
exaly +4 more sources
Imidazopyrazinone is a typical scaffold present in marine bioluminescence, in which thermal energy is converted into excitation energy in an enzyme-catalyzed reaction.
Carla M MAGALHÃES +2 more
exaly +4 more sources
Biochemical and Biophysical Research Communications
Dehydrocoelenterazine (dCTZ) is a dehydrogenated form of coelenterazine (CTZ), which is well-known as the luciferin responsible for the bioluminescence reaction in marine organisms.
Satoshi Inouye +4 more
semanticscholar +3 more sources
Dehydrocoelenterazine (dCTZ) is a dehydrogenated form of coelenterazine (CTZ), which is well-known as the luciferin responsible for the bioluminescence reaction in marine organisms.
Satoshi Inouye +4 more
semanticscholar +3 more sources
Coelenterazine sulfotransferase from the luminous squid Watasenia scintillans.
Biochemical and Biophysical Research CommunicationsThe squid Watasenia scintillans is a luminous marine organism that utilizes coelenterazine 2,6-disulfate (CTZ 2,6-SO3H) as its luminous substrate. CTZ 2,6-SO3H, a derivative of coelenterazine (CTZ), can be chemically synthesized by sulfating CTZ at its ...
Nowshin Farjana +3 more
semanticscholar +3 more sources
New red-shifted coelenterazine analogues with an extended electronic conjugation
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 ...
Germano Giuliani +2 more
exaly +2 more sources
Coelenterazine (CLZn; 3, 7-dihydro-2-(p-hydroxybenzyl)-6-(p-hydroxyphenyl)-8-benzylimidazolo++ +[1 ,2-a]pyrazin-3-one), the substrate for bioluminescence reactions in many marine animals, is endowed with high antioxidant properties.
Jacqueline Marchand-Brynaert +2 more
exaly +2 more sources
Ca2+-regulated photoproteins responsible for bioluminescence of a variety of marine organisms are single-chain globular proteins within the inner cavity of which the oxygenated coelenterazine, 2-hydroperoxycoelenterazine, is tightly bound. Alongside with
Elena V Eremeeva +2 more
exaly +2 more sources
Three Efficient Methods for Preparation of Coelenterazine Analogues
Chemistry - A European Journal, 2016AbstractThe growing popularity of bioluminescent assays has highlighted the need for coelenterazine analogues possessing properties tuned for specific applications. However, the structural diversity of known coelenterazine analogues has been limited by current syntheses. Known routes for the preparation of coelenterazine analogues employ harsh reaction
Mary P Hall +2 more
exaly +3 more sources
Coelenterazine-dependent luciferases
Biochemistry (Moscow), 2015Bioluminescence is a widespread natural phenomenon. Luminous organisms are found among bacteria, fungi, protozoa, coelenterates, worms, molluscs, insects, and fish. Studies on bioluminescent systems of various organisms have revealed an interesting feature - the mechanisms underlying visible light emission are considerably different in representatives ...
S V, Markova, E S, Vysotski
openaire +2 more sources
Biochemical and Biophysical Research Communications - BBRC, 2023
Coelenterazine (CTZ) is known as a light-emitting source for the bioluminescence reaction in marine organisms. CTZ has two phenolic hydroxy groups at the C2-benzyl and C6-phenyl positions, and a keto-enol type hydroxy group at the C3-position in the core
S. Inouye +2 more
semanticscholar +1 more source
Coelenterazine (CTZ) is known as a light-emitting source for the bioluminescence reaction in marine organisms. CTZ has two phenolic hydroxy groups at the C2-benzyl and C6-phenyl positions, and a keto-enol type hydroxy group at the C3-position in the core
S. Inouye +2 more
semanticscholar +1 more source
Organic Preparations and Procedures International, 2001
(2001). SYNTHESIS OF COELENTERAZINE. Organic Preparations and Procedures International: Vol. 33, No. 5, pp. 477-485.
Maciej Adamczyk +4 more
openaire +1 more source
(2001). SYNTHESIS OF COELENTERAZINE. Organic Preparations and Procedures International: Vol. 33, No. 5, pp. 477-485.
Maciej Adamczyk +4 more
openaire +1 more source

