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(1E)-2-methyl-4-(2,3,6-trimethylphenyl)but-1-en-1-yl formate + O2
4-(2,3,6-trimethylphenyl)butan-2-one + CO2 + formate
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Substrates: -
Products: -
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(1E)-2-methyl-4-(2,4,5-trimethylphenyl)but-1-en-1-yl formate + O2
4-(2,4,5-trimethylphenyl)butan-2-one + CO2 + formate
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Substrates: -
Products: -
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(1E)-2-methyl-4-(2,4,5-trimethylphenyl)but-1-en-1-yl formate + reduced electron acceptor + O2
4-(2,4,5-trimethylphenyl)butane-2-one + CO2 + formate + electron acceptor + H2O + hv
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Substrates: -
Products: -
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(1E)-2-methyl-4-(2,6,6-trimethylcyclohex-1-en-1-yl)but-1-en-1-yl 4-(methylamino)benzoate + O2
4-(2,6,6-trimethylcyclohex-1-en-1-yl)butan-2-one + CO2 + 4-(methylamino)benzaldehyde
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Substrates: -
Products: -
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(1E)-2-methyl-4-(2,6,6-trimethylcyclohex-1-en-1-yl)but-1-en-1-yl 4-cyanobenzoate + O2
4-(2,6,6-trimethylcyclohex-1-en-1-yl)butan-2-one + CO2 + 4-cyanobenzaldehyde
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Substrates: -
Products: -
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(1E)-2-methyl-4-(2,6,6-trimethylcyclohex-1-en-1-yl)but-1-en-1-yl 4-methoxybenzoate + O2
4-(2,6,6-trimethylcyclohex-1-en-1-yl)butan-2-one + CO2 + 4-methoxybenzaldehyde
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Substrates: -
Products: -
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(1E)-2-methyl-4-(2,6,6-trimethylcyclohex-1-en-1-yl)but-1-en-1-yl 4-nitrobenzoate + O2
4-(2,6,6-trimethylcyclohex-1-en-1-yl)butan-2-one + CO2 + 4-nitrobenzaldehyde
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Substrates: -
Products: -
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(1E)-2-methyl-4-(2,6,6-trimethylcyclohex-1-en-1-yl)but-1-en-1-yl acetate + O2
4-(2,6,6-trimethylcyclohex-1-en-1-yl)butan-2-one + CO2 + acetaldehyde
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Substrates: -
Products: -
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(1E)-2-methyl-4-(2,6,6-trimethylcyclohex-1-en-1-yl)but-1-en-1-yl benzoate + O2
4-(2,6,6-trimethylcyclohex-1-en-1-yl)butan-2-one + CO2 + benzaldehyde
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Substrates: -
Products: -
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(1E)-2-methyl-4-(2,6,6-trimethylcyclohex-1-en-1-yl)but-1-en-1-yl formate + O2
4-(2,6,6-trimethylcyclohex-1-en-1-yl)butan-2-one + CO2 + formate
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Substrates: -
Products: -
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(1E)-4-(2,6-dimethylphenyl)-2-methylbut-1-en-1-yl formate + O2
4-(2,6-dimethylphenyl)butan-2-one + CO2 + formate
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Substrates: -
Products: -
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(1E)-4-(2,6-dimethylphenyl)-2-methylbut-1-en-1-yl formate + reduced electron acceptor + O2
4-(2,6-dimethylphenyl)butane-2-one + CO2 + formate + electron acceptor + H2O + hv
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Substrates: -
Products: -
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(1E)-4-mesityl-2-methylbut-1-en-1-yl formate + reduced electron acceptor + O2
4-mesitylbutane-2-one + CO2 + formate + electron acceptor + H2O + hv
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Substrates: -
Products: -
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(E)-2-methyl-4-(2,6,6-trimethyl-1-cyclohex-1-yl)-1-buten-1-ol-formate + NADH + O2
oxidized Latia luciferin + NAD+ + CO2 + H2O + formate + light
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Substrates: trivial name Latia luciferin
Products: -
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Latia luciferin + AH2 + O2
oxidized Latia luciferin + CO2 + formate + A + H2O + hnu
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Substrates: -
Products: -
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Latia luciferin + reduced electron acceptor + O2
oxidized Latia luciferin + CO2 + formate + electron acceptor + H2O + hv
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Substrates: -
Products: -
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Bacteriuria
Evaluation of a rapid bacterial ATP assay for screening BAL samples from ICU patients submitted for quantitative bacterial cultures.
Carcinoma
Swelling-activated, cystic fibrosis transmembrane conductance regulator-augmented ATP release and Cl- conductances in murine C127 cells.
Cystic Fibrosis
Swelling-activated, cystic fibrosis transmembrane conductance regulator-augmented ATP release and Cl- conductances in murine C127 cells.
Influenza, Human
Investigation on cellular uptake and pharmacodynamics of DOCK2-inhibitory peptides conjugated with cell-penetrating peptides.
Multiple Myeloma
[ATP and ADP of platelets in chronic myeloproliferative disorders and multiple myeloma]
Myeloproliferative Disorders
[ATP and ADP of platelets in chronic myeloproliferative disorders and multiple myeloma]
Neoplasms
Enhancement of PSMA-Directed CAR Adoptive Immunotherapy by PD-1/PD-L1 Blockade.
Neoplasms
EPR Oximetry Sensor-Developing a TAM Derivative for In Vivo Studies.
Neoplasms
The potential of 5-fluorocytosine/cytosine deaminase enzyme prodrug gene therapy in an intrahepatic colon cancer model.
Neoplasms
[In vitro chemosensitivity testing evaluated by intracellular ATP level: ATP assay]
Pyuria
Urinary ATP as an indicator of infection and inflammation of the urinary tract in patients with lower urinary tract symptoms.
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Shimomura, O.; Johnson, F.H.; Kohama, Y.
Reactions involved in bioluminescence systems of limpet (Latia neritoides) and luminous bacteria
Proc. Natl. Acad. Sci. USA
69
2086-2089
1972
Latia neritoides
brenda
Shimomura, O.; Johnson, F.H.
The structure of Latia luciferin
Biochemistry
7
1734-1738
1968
Latia neritoides
brenda
Nakamura, M.; Mamino, M.; Masaki, M.; Maki, S.; Matsui, R.; Kojima, S.; Hirano, T.; Ohmiya, Y.; Niwa, H.
Bioluminescence activity of Latia luciferin analogues: replacement of the 2,6,6-trimethylcyclohexene ring onto the methyl-substituted phenyl groups
Tetrahedron Lett.
46
53-56
2004
Latia neritoides
-
brenda
Ohmiya, Y.; Kojima, S.; Nakamura, M.; Niwa, H.
Bioluminescence in the limpet-like snail, Latia neritoides
Bull. Chem. Soc. Jpn
78
1197-1205
2005
Latia neritoides
-
brenda
Shimomura, O.; Johnson, F.; Haneda, Y.
Isolation of the lucifer in of the New Zealand fresh-water limpet, Latia neritoides gray
Biolumin. Progr.
2015
391-404
2015
Latia neritoides
-
brenda
Kaskova, Z.M.; Tsarkova, A.S.; Yampolsky, I.V.
1001 lights luciferins, luciferases, their mechanisms of action and applications in chemical analysis, biology and medicine
Chem. Soc. Rev.
45
6048-6077
2016
Latia neritoides
brenda
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