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Unknown
(313)
Proteomics
(6)
Transcriptomics
(2)
Genomics
(1)
Metabolomics
(1)
Organisms
Homo sapiens
(3)
Mus musculus
(2)
Pyricularia oryzae 70-15
(2)
Arabidopsis thaliana
(1)
Mus sp.
(1)
Repository
iProX
(3)
pride
(3)
biostudies-arrayexpress
(2)
EGA
(1)
MetaboLights
(1)
Tissue
Mycelium
(2)
Lung
(1)
Uterine endometrium
(1)
Technology Type
Data-dependent acquisition
(3)
Mass Spectrometry
(3)
Mass spectrometry
(1)
Bottom-up proteomics
(1)
Instrument Platform
Liquid Chromatography MS -
(1)
Publication Date
2025
(5)
2016
(1)
2011
(1)
2021
(1)
2026
(1)
Metabolite Name
(+)-Prosopinine
(1)
(+/-)-Bocconarborine A
(1)
(+/-)-Bocconarborine B
(1)
(1-((1-Methylpiperidin-2-yl)methyl)-1H-indol-3-yl)(naphthalen-1-yl)methanone
(1)
(1-hexyl-5-phenyl-1H-pyrrol-3-yl)(naphthalen-1-yl)methanone
(1)
(10)-Gingerol
(1)
(1R,12S,16Z,24E,26E,28Z,32S)-1,18-dihydroxy-12-[1-(4-hydroxy-3-methoxycyclohexyl)propan-2-yl]-19,30-dimethoxy-15,17,21,23,29,35-hexamethyl-11,36-dioxa-4-azatricyclo[30.3.1.0,]hexatriaconta-16,24,26,28-tetraene-2,3,10,14,20-pentone
(1)
(1R,16Z,24E,26E,28Z)-1,18-dihydroxy-12-[1-(4-hydroxy-3-methoxycyclohexyl)propan-2-yl]-29-(hydroxymethyl)-19,30-dimethoxy-15,17,21,23,35-pentamethyl-11,36-dioxa-4-azatricyclo[30.3.1.0,]hexatriaconta-16,24,26,28-tetraene-2,3,10,14,20-pentone
(1)
(1R,2R,5Z,12R,13S,16Z)-25-(9H-pyrido[3,4-b]indol-1-yl)-11,22-diazapentacyclo[11.11.2.12,22.02,12.04,11]heptacosa-5,16,25-trien-13-ol
(1)
(1R,2S,13S,16S,17S,19R,20R,22S,25S,27S)-1,2,24,24-tetramethyl-8,9-bis(3-methylbut-2-enyl)-22-(2-methylprop-1-enyl)-18,21,23,26-tetraoxa-4-azaoctacyclo[14.13.0.02,13.03,11.05,10.017,19.017,27.020,25]nonacosa-3(11),5(10),6,8-tetraen-16-ol
(1)
(1R,2S,4S,6R,7S,8R,9S,12S,13S,18S)-6-methoxy-7,9,13-trimethyl-6-[(3S)-3-methyl-4-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybutyl]-5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosan-16-one
(1)
(1R,3S,6S,7E,13S,16R,17R,21S,22S)-17-[(2R,4R,5S,6R)-5-[(2S,4R,5S,6R)-4,5-dihydroxy-6-methyloxan-2-yl]oxy-4-hydroxy-6-methyloxan-2-yl]oxy-28-hydroxy-3,22-dimethyl-23,26-dioxo-24,27-dioxapentacyclo[23.2.1.01,6.013,22.016,21]octacosa-4,7,14,25(28)-tetraene-4-carboxylic acid
(1)
(1S,2R,4aR,6aS,6bR,12aS,12bR,14bR)-1,2,4a,6a,6b,9,12a-Heptamethyl-1,2,3,4,4a,5,6,6a,6b,7,8,8a,11,12,12a,12b,13,14b-octadecahydropicene
(1)
(1S,2S,6R,7S,9R,10R,11R)-1,4,4-trimethyl-8,13-dioxatetracyclo[8.2.1.02,6.07,11]tridecane-9,10-diol
(1)
(1S,3R)-5-[3-[4-[(1S,3R)-6,8-dihydroxy-1,3-dimethyl-1,2,3,4-tetrahydroisoquinolin-5-yl]-1-hydroxy-8-methoxy-6-methylnaphthalen-2-yl]-4-hydroxy-5-methoxy-7-methylnaphthalen-1-yl]-1,3-dimethyl-1,2,3,4-tetrahydroisoquinoline-6,8-diol
(1)
(1S,3Z,5R,7R)-3-[(3,4-dihydroxyphenyl)-hydroxy-methylene]-1-[(2S)-2-isopropenyl-5-methyl-hex-4-enyl]-6,6-dimethyl-5,7-bis(3-methylbut-2-enyl)bicyclo[3.3.1]nonane-2,4,9-trione
(1)
(1S,4R)-1,7,7-trimethylbicyclo[2.2.1]heptane-2,3-dione
(1)
(1aR,7aS,10aS,10bS)-1a,5-dimethyl-8-methylidene-2,3,6,7,7a,8,10a,10b-octahydrooxireno[9,10]cyclodeca[1,2-b]furan-9(1aH)-one
(1)
(2-Chloro-benzyl)-pyridin-3-ylmethyl-amine
(1)
(2-Iodophenyl)(1-((1-methylpiperidin-2-yl)methyl)-1H-indol-3-yl)methanone
(1)
(2-methoxy-4-{2-[(1R,16Z,24E,26E,28Z)-1,18,19-trihydroxy-30-methoxy-15,17,21,23,29,35-hexamethyl-2,3,10,14,20-pentaoxo-11,36-dioxa-4-azatricyclo[30.3.1.0,]hexatriaconta-16,24,26,28-tetraen-12-yl]propyl}cyclohexyl)oxidanesulfonic acid
(1)
(2-{[3-(3,4-Dihydroxy-5-methoxyphenyl)prop-2-enoyl]oxy}ethyl)trimethylazanium
(1)
(23S)-23,25,26-trihydroxycalciol
(1)
(25S)-26-Hydroxy-24-methylenecycloartan-3-one
(1)
(2R)-2-[(2R,3R,4S)-3,4-bis(2-hydroxyethoxy)oxolan-2-yl]-2-hydroxyethyl dodecanoate
(1)
(2R)-2-hydroxy-N-[(2S,3R,4E,8E)-3-hydroxy-1-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyhexadeca-4,8-dien-2-yl]tetracosanamide
(1)
(2R)-O-phospho-3-sulfolactic acid
(1)
(2R,13R,14S,15S,17S)-17-hydroxy-2,13,14,15-tetramethyl-14-propanoyltetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadeca-3,6-dien-5-one
(1)
(2R,3S,5S,8R,9S,10S,13S,17R)-17-[(2S,3R,4R,5S)-3,4-dihydroxy-5,6-dimethylheptan-2-yl]-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthrene-2,3-diol
(1)
(2S)-2-[[(2R,3R)-3-azaniumyl-2-hydroxy-4-phenylbutanoyl]amino]-4-methylpentanoate
(1)
Study type
Transcription profiling by array
(1)
RNA-seq of coding RNA
(1)
Release Date
2025
(79)
2024
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2022
(34)
2023
(32)
2021
(29)
2020
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2026
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2019
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2016
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2018
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2017
(4)
2015
(3)
2011
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2012
(2)
2014
(1)
2013
(1)
2010
(1)
2009
(1)
2008
(1)
Lab affiliation
College of Agronomy, Jiangxi Agricultural University
(2)
Chair of Proteomics and Bioanalytics, Technical University of Munich, Bavaria, Germany
(1)
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Multimodal AI for prediction of distant metastasis in carcinoma patients.
Not available
S-EPMC10203594
|
biostudies-literature
Cite
A generative AI-discovered TNIK inhibitor for idiopathic pulmonary fibrosis: a randomized phase 2a trial.
Not available
S-EPMC12353801
|
biostudies-literature
Cite
Integrating AI into clinical education: evaluating general practice trainees' proficiency in distinguishing AI-generated hallucinations and impacting factors.
Not available
S-EPMC11924592
|
biostudies-literature
Cite
AI-Assisted Drug Re-Purposing for Human Liver Fibrosis.
Not available
S-EPMC12667525
|
biostudies-literature
Cite
Impact of AI-Assisted Diagnosis on American Patients' Trust in and Intention to Seek Help From Health Care Professionals: Randomized, Web-Based Survey Experiment.
Not available
S-EPMC12222559
|
biostudies-literature
Cite
Assessment of AI-Based Protein Structure Prediction for the NLRP3 Target.
Not available
S-EPMC9505260
|
biostudies-literature
Cite
Structure of Fam20A reveals a pseudokinase featuring a unique disulfide pattern and inverted ATP-binding.
Not available
S-EPMC5413348
|
biostudies-literature
Cite
A novel AI-powered radiographic analysis surpasses specialists in stage II-IV periodontitis detection: a multicenter diagnostic study.
Not available
S-EPMC12627451
|
biostudies-literature
Cite
Biochemical and Computational Characterization of Haloalkane Dehalogenase Variants Designed by Generative AI: Accelerating the S<sub>N</sub>2 Step.
Not available
S-EPMC12445222
|
biostudies-literature
Cite
A robust and efficient AI assistant for breast tumor segmentation from DCE-MRI via a spatial-temporal framework.
Not available
S-EPMC10499873
|
biostudies-literature
Cite
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