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Unknown
(20)
Metabolomics
(1)
Repository
MetaboLights
(1)
Technology Type
Mass spectrometry
(1)
Instrument Platform
Liquid Chromatography MS - negative - reverse phase
(1)
Publication Date
2025
(1)
CHEBI ID
CHEBI:133460
(1)
CHEBI:136619
(1)
CHEBI:1369
(1)
CHEBI:141700
(1)
CHEBI:144145
(1)
CHEBI:145096
(1)
CHEBI:145828
(1)
CHEBI:15834
(1)
CHEBI:15864
(1)
CHEBI:15932
(1)
CHEBI:16112
(1)
CHEBI:16164
(1)
CHEBI:16243
(1)
CHEBI:16514
(1)
CHEBI:167540
(1)
CHEBI:167928
(1)
CHEBI:167992
(1)
CHEBI:168532
(1)
CHEBI:169040
(1)
CHEBI:16914
(1)
CHEBI:17189
(1)
CHEBI:17224
(1)
CHEBI:173769
(1)
CHEBI:17445
(1)
CHEBI:17488
(1)
CHEBI:174991
(1)
CHEBI:17521
(1)
CHEBI:17574
(1)
CHEBI:17594
(1)
CHEBI:176204
(1)
Metabolite Name
(4-Hydroxyanilino)-oxobutanoic acid
(1)
2',4',6'-Trihydroxydihydrochalcone
(1)
2',4-Dihydroxy-3,4',6'-trimethoxychalcone
(1)
2,3,4-Trihydroxybenzoic acid
(1)
3',4',7-Trihydroxyflavanone
(1)
3,4-Dehydro-6-hydroxymellein
(1)
3-Hydroxybenzoic acid
(1)
3-Hydroxyphenylacetic acid
(1)
3-Methylcatechol
(1)
3-O-Feruloylquinic acid
(1)
4-Acetoxyphenol
(1)
4-Hydroxy-3-prenylbenzoic acid
(1)
4-Hydroxybenzoic acid
(1)
4-Hydroxyphenylacetic acid
(1)
4-Methoxycinnamic acid
(1)
4-Methylumbelliferone
(1)
5,6,2'-Trimethoxyflavone
(1)
5,7,3,4-Tetrahydroxy-6,8-dimethoxyflavone
(1)
5-Hydroxy-6,8-dimethoxy-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-2-one
(1)
?-Guaiaconic acid
(1)
?-L-Glutaminyl-4-hydroxybenzene
(1)
Acetylgenistin
(1)
Apigenin / Genistein
(1)
Apiin
(1)
Baicalein
(1)
Benzoic acid
(1)
Biochanin A
(1)
Butin
(1)
Caffeic acid
(1)
Caffeic acid hexoside
(1)
Release Date
2017
(6)
2025
(3)
2022
(2)
2020
(2)
2019
(2)
2018
(2)
2024
(1)
2023
(1)
2015
(1)
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Towards synthetic catechol rich protein analogues through tyrosinase catalyzed activation of a tyrosine dipeptide in continuous mode.
Not available
S-EPMC12573765
|
biostudies-literature
Cite
Polymerizing Like Mussels Do: Toward Synthetic Mussel Foot Proteins and Resistant Glues.
Not available
S-EPMC6282983
|
biostudies-literature
Cite
Beyond Phenolics: Alternative Substrates for Type III Copper Enzymes.
Not available
S-EPMC12002105
|
biostudies-literature
Cite
Identification of Amino Acid Residues Responsible for C-H Activation in Type-III Copper Enzymes by Generating Tyrosinase Activity in a Catechol Oxidase.
Not available
S-EPMC7693034
|
biostudies-literature
Cite
Heterologous expression and characterization of functional mushroom tyrosinase (AbPPO4).
Not available
S-EPMC5431950
|
biostudies-literature
Cite
Extraction, Purification, and Characterization of Olive (<i>Olea europaea</i> L., cv. Chemlal) Polyphenol Oxidase.
Not available
S-EPMC10870767
|
biostudies-literature
Cite
In crystallo activity tests with latent apple tyrosinase and two mutants reveal the importance of the mutated sites for polyphenol oxidase activity.
Not available
S-EPMC5544008
|
biostudies-literature
Cite
Biochemical characterization of Dimocarpus longan polyphenol oxidase provides insights into its catalytic efficiency.
Not available
S-EPMC9700842
|
biostudies-literature
Cite
Three recombinantly expressed apple tyrosinases suggest the amino acids responsible for mono- versus diphenolase activity in plant polyphenol oxidases.
Not available
S-EPMC5562730
|
biostudies-literature
Cite
A Peptide-Induced Self-Cleavage Reaction Initiates the Activation of Tyrosinase.
Not available
S-EPMC6563526
|
biostudies-literature
Cite
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