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Unknown
(13)
Metabolomics
(1)
Repository
MetaboLights
(1)
Technology Type
Mass spectrometry
(1)
Instrument Platform
Liquid Chromatography MS - negative - reverse phase
(1)
Liquid Chromatography MS - positive - reverse phase
(1)
Publication Date
2023
(1)
CHEBI ID
CHEBI:10037
(1)
CHEBI:10072
(1)
CHEBI:1015
(1)
CHEBI:10276
(1)
CHEBI:107646
(1)
CHEBI:108592
(1)
CHEBI:108595
(1)
CHEBI:109547
(1)
CHEBI:109895
(1)
CHEBI:110163
(1)
CHEBI:114185
(1)
CHEBI:114196
(1)
CHEBI:116314
(1)
CHEBI:122
(1)
CHEBI:125539
(1)
CHEBI:12962
(1)
CHEBI:131762
(1)
CHEBI:131914
(1)
CHEBI:132629
(1)
CHEBI:132639
(1)
CHEBI:132823
(1)
CHEBI:132958
(1)
CHEBI:133086
(1)
CHEBI:13332
(1)
CHEBI:133542
(1)
CHEBI:134355
(1)
CHEBI:135010
(1)
CHEBI:135679
(1)
CHEBI:141315
(1)
CHEBI:141964
(1)
Metabolite Name
(+-)-Baclofen
(1)
(3E)-3-Benzylidene-4-Methyl-1H-1,4-Benzodiazepine-2,5-Dione
(1)
(5R)-5-Hydroxy-1-(4-Hydroxy-3-Methoxyphenyl)Tetradecan-3-One
(1)
(R)-3-Hydroxybutanoate
(1)
1,2-Dihydroxyheptadec-16-En-4-Yl Acetate
(1)
1,3-Dideacetyl-7-Deacetoxy-7-Oxokhivorin
(1)
1,4-Cyclohexanedicarboxylic Acid
(1)
1,8,9-Anthracenetriol
(1)
1-Hydroxy-2-Naphthoic Acid
(1)
1-Hydroxyanthraquinone
(1)
16-Hydroxypalmitate
(1)
2,4-Dihydroxybenzophenone
(1)
2,4-Dinitrophenol
(1)
2,5-Dihydroxy-3-Undecylcyclohexa-2,5-Diene-1,4-Dione
(1)
2-Hydroxybenzaldehyde
(1)
2-Hydroxyisocaproic Acid
(1)
2-Naphthalene Sulfonic Acid
(1)
2-Oxoglutarate
(1)
3,4,5-Trimethoxycinnamic Acid
(1)
3-(4-Hydroxyphenyl)lactate
(1)
3-(Hydroxymethyl)Phenol
(1)
3-Chlorotyrosine
(1)
3-Deoxysappanchalcone
(1)
3-Hydroxy-3-methylglutarate
(1)
3-Indoxyl Sulfate
(1)
3-Methylxanthine
(1)
3-Phenyllactic Acid
(1)
3-Phospho-D-Glycerate
(1)
3-Sulfino-L-Alanine
(1)
4,4`-Thiodiphenol
(1)
Release Date
2021
(3)
2022
(2)
2020
(2)
2026
(1)
2024
(1)
2023
(1)
2019
(1)
2018
(1)
2017
(1)
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Promoting Singlet/triplet Exciton Transformation in Organic Optoelectronic Molecules: Role of Excited State Transition Configuration.
Not available
S-EPMC5524908
|
biostudies-literature
Cite
Single-component color-tunable circularly polarized organic afterglow through chiral clusterization.
Not available
S-EPMC8776763
|
biostudies-literature
Cite
Design of highly efficient deep-blue organic afterglow through guest sensitization and matrices rigidification.
Not available
S-EPMC7511363
|
biostudies-literature
Cite
Ectomycorrhizal fungi recruit hyphae-associated bacteria that metabolize thiamine to promote pine symbiosis.
Not available
S-EPMC12815266
|
biostudies-literature
Cite
On-demand modulating afterglow color of water-soluble polymers through phosphorescence FRET for multicolor security printing.
Not available
S-EPMC9012460
|
biostudies-literature
Cite
Direct population of triplet excited states through singlet-triplet transition for visible-light excitable organic afterglow.
Not available
S-EPMC6530535
|
biostudies-literature
Cite
Direct Population of Triplet States for Efficient Organic Afterglow through the Intra/Intermolecular Heavy-Atom Effect.
Not available
S-EPMC10934877
|
biostudies-literature
Cite
Constructing Donor-Resonance-Donor Molecules for Acceptor-Free Bipolar Organic Semiconductors.
Not available
S-EPMC11014465
|
biostudies-literature
Cite
Near-Infrared-Excitable Organic Ultralong Phosphorescence through Multiphoton Absorption.
Not available
S-EPMC7877391
|
biostudies-literature
Cite
Fluorine-induced aggregate-interlocking for color-tunable organic afterglow with a simultaneously improved efficiency and lifetime.
Not available
S-EPMC8179499
|
biostudies-literature
Cite
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