Chen Li-Chang LC

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Unknown (225)
Proteomics (20)
Metabolomics (12)
Transcriptomics (1)
Other (1)
Multiomics (1)

Organisms

Homo sapiens (7)
Bos taurus (2)
Acinetobacter baylyi ADP1 (2)
Escherichia coli (2)
Capra hircus (1)
Enterococcus faecalis (1)
Mus musculus (1)
Oryctolagus cuniculus (1)
Rattus norvegicus (1)
Saccharomyces cerevisiae (1)

Repository

pride (16)
MetaboLights (12)
iProX (2)
MassIVE (2)
biostudies-arrayexpress (1)
GPMDB (1)

Tissue

Testis (2)
Blood (1)
Blood cell (1)
Blood plasma (1)
Bone marrow (1)
Cell culture (1)
Colon (1)
Haploid cell (1)
HeLa cell (1)
Heart (1)
Liver (1)
Pancreas (1)
Permanent cell line cell (1)
Prostate gland (1)
Small intestine (1)
Spleen (1)

Disease

Not Available (1)
Breast cancer (1)
Severe acute respiratory syndrome (1)

Technology Type

Mass Spectrometry (16)
Mass spectrometry (12)
Shotgun proteomics (6)
Bottom-up proteomics (4)
Affinity purification coupled with mass spectrometry proteomics (1)
Chemical cross-linking coupled with mass spectrometry proteomics (1)
Data-independent acquisition (1)
Gel-based experiment (1)
MSE (1)
Proteogenomics (1)

Instrument Platform

Liquid Chromatography MS - negative - reverse-phase (5)
Liquid Chromatography MS - negative - reverse phase (4)
Liquid Chromatography MS - positive - reverse phase (4)
Liquid Chromatography MS - positive - reverse-phase (4)
Liquid Chromatography MS - positive (2)
Instrument (1)
LTQ Orbitrap Elite (1)
Q Exactive HF-X (1)
Liquid Chromatography MS - negative (1)

Publication Date

2026 (9)
2021 (5)
2022 (4)
2023 (4)
2020 (2)
2019 (2)
2024 (2)
2012 (1)
2025 (1)
2018 (1)
2016 (1)
2014 (1)

CHEBI ID

CHEBI:136063 (2)
CHEBI:45956 (2)
CHEBI:67021 (2)
CHEBI:72959 (2)
CHEBI:72962 (2)
CHEBI:88601 (2)
CHEBI:89279 (2)
CHEBI:89823 (2)
CHEBI:10049 (1)
CHEBI:10093 (1)
CHEBI:101085 (1)
CHEBI:109895 (1)
CHEBI:1109 (1)
CHEBI:116314 (1)
CHEBI:12387 (1)
CHEBI:124991 (1)
CHEBI:125535 (1)
CHEBI:127309 (1)
CHEBI:131428 (1)
CHEBI:131430 (1)
CHEBI:131439 (1)
CHEBI:131440 (1)
CHEBI:131590 (1)
CHEBI:131887 (1)
CHEBI:131924 (1)
CHEBI:131988 (1)
CHEBI:132448 (1)
CHEBI:13248 (1)
CHEBI:132503 (1)
CHEBI:132539 (1)

Metabolite Name

(+)-Catechin (1)
(+)-Gallocatechin (1)
(-)-Epicatechin (1)
(1'S,2R,2'R,10'S,11'S,15'S)-17'-hydroxy-2',15'-dimethylspiro[oxolane-2,14'-tetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadecane]-6',8'-diene-5,5'-dione (1)
(1-{1-[(4-hydroxy-3-methoxyphenyl)methyl]-7,8-dimethoxy-2,2-dimethyl-1,2,3,4-tetrahydro-2λ⁵-isoquinolin-2-yl}ethylidene)-λ⁴-oxidanyliumyl (1)
(10,14a-dihydroxy-2,2,4a,6a,6b,9,9,12a-octamethyl-docosahydropicen-13-yl)oxidanesulfonic acid (1)
(10S,14S)-10,14,20-trimethyl-16-methylidene-22-azahexacyclo[12.10.0.0²,¹¹.0⁵,¹⁰.0¹⁵,²³.0¹⁷,²²]tetracosan-5-ylium-7-olate (1)
(12aR)-4-(dimethylamino)-4a,5,10,12a-tetrahydroxy-6-methylidene-1,2,3,4,4a,5,5a,6,11,11a,12,12a-dodecahydrotetracene-1,3,11,12-tetrone (1)
(12aR)-7-chloro-4-(dimethylamino)-4,6,10,12a-tetrahydroxy-1,2,3,4,4a,5,5a,6,11,11a,12,12a-dodecahydrotetracene-1,3,11,12-tetrone (1)
(12aS)-4,7-bis(dimethylamino)-10,12,12a-trihydroxy-1,3,11-trioxo-9-(2-oxoacetamido)-1,2,3,4,4a,5,5a,6,11,11a,12,12a-dodecahydrotetracene-2-carboximidic acid (1)
(12aS)-9-{[2-(tert-butylamino)-1-hydroxyethylidene]amino}-4,7-bis(dimethylamino)-5,10,12,12a-tetrahydroxy-1,3,11-trioxo-1,2,3,4,4a,5,5a,6,11,12a-decahydrotetracene-2-carboximidic acid (1)
(13-{[5-(acetyloxy)-3,4-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1,6,6,11,15-pentamethyl-14-(6-methylhept-5-en-2-yl)-5-[(3,4,5-trihydroxyoxan-2-yl)oxy]tetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadec-7-en-9-yl)oxidanesulfonic acid (1)
(13R)-5-(3,4-dihydroxyphenyl)-6,9,17,19,21-pentahydroxy-13-(4-hydroxyphenyl)-4,12,14-trioxapentacyclo[11.7.1.0²,¹¹.0³,⁸.0¹⁵,²⁰]henicosa-2(11),3(8),5,9,15,17,19-heptaen-7-one (1)
(15Z)-Octadec-15-en-9,11,13-triynoic acid (1)
(1R)-1,4-bis({[(2E)-3-(3,4-dihydroxyphenyl)prop-2-enoyl]oxy})-3-hydroxy-5-(sulfooxy)cyclohexane-1-carboxylic acid (1)
(1R,16Z,24E,26E,28Z)-1,18,26,27-tetrahydroxy-19,30-dimethoxy-12-[1-(3-methoxy-4-oxocyclohexyl)propan-2-yl]-15,17,21,23,29,35-hexamethyl-11,36-dioxa-4-azatricyclo[30.3.1.0⁴,⁹]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]-19,30-dimethoxy-15,17,21,23,29-pentamethyl-35-methylidene-11,36-dioxa-4-azatricyclo[30.3.1.0⁴,⁹]hexatriaconta-16,24,26,28-tetraene-2,3,10,14,20-pentone (1)
(1R,2R,3R,11S,12S,14R,26R)-5,6',7',12-tetrahydroxy-6-methoxy-7,21,30-trimethyl-27-oxo-3',4'-dihydro-2'H-17,19,28-trioxa-24-thia-13,30-diazaspiro[heptacyclo[12.9.6.1³,¹¹.0²,¹³.0⁴,⁹.0¹⁵,²³.0¹⁶,²⁰]triacontane-26,1'-isoquinoline]-4(9),5,7,15(23),16(20),21-hexaen-22-yl acetate (1)
(1R,2S,3R,4R,5S,6R,7S)-1,3,4,5,7,8,9,10,10-Nonachlorotricyclo[5.2.1.0²,⁶]dec-8-ene (1)
(1R,6S,12R,15S)-5,5-Dimethyl-11,13-dioxatetracyclo[7.5.1.0¹,⁶.0¹²,¹⁵]pentadec-8-ene (1)
(1R,9S,18Z,24R)-12-[1-(4-chloro-3-hydroxycyclohexyl)prop-1-en-2-yl]-17-ethyl-1,14-dihydroxy-23,25-dimethoxy-13,19,21,27-tetramethyl-11,28-dioxa-4-azatricyclo[22.3.1.0⁴,⁹]octacos-18-ene-2,3,10,16-tetrone (1)
(1R,9S,18Z,24R)-12-[1-(4-chloro-3-methoxycyclohexyl)prop-1-en-2-yl]-17-ethyl-1,14-dihydroxy-13-(hydroxymethyl)-23,25-dimethoxy-19,21,27-trimethyl-11,28-dioxa-4-azatricyclo[22.3.1.0⁴,⁹]octacos-18-ene-2,3,10,16-tetrone (1)
(1S)-1,3,4-trihydroxy-5-(sulfooxy)cyclohexane-1-carboxylic acid (1)
(1S,16Z,24E,26E,28Z)-1,18-dihydroxy-12-{1-[4-(2-hydroxyethoxy)-3-methoxycyclohexyl]propan-2-yl}-15-(hydroxymethyl)-19,30-dimethoxy-17,21,23,29,35-pentamethyl-11,36-dioxa-4-azatricyclo[30.3.1.0⁴,⁹]hexatriaconta-16,24,26,28-tetraene-2,3,10,14,20-pentone (1)
(1S,16Z,24E,26E,28Z)-1,18-dihydroxy-12-{1-[4-(2-hydroxyethoxy)-5-methoxy-2-oxocyclohexyl]propan-2-yl}-19,30-dimethoxy-15,17,21,23,29,35-hexamethyl-11,36-dioxa-4-azatricyclo[30.3.1.0⁴,⁹]hexatriaconta-16,24,26,28-tetraene-2,3,10,14,20-pentone (1)
(1S,2R,10S,11S,14R,15R)-2,15-Dimethyl-14-[(2R)-6-methylheptan-2-yl]tetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadec-7-ene (1)
(1S,2S,10S,11S,15R)-14-(5,6-dimethylheptan-2-yl)-2,15-dimethyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadecane-5,17-diol (1)
(1S,2S,5R,7R,10S,11S,14R,15S,17S)-14-[(1R)-1,2-Dihydroxyethyl]-2,15-dimethyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadecane-5,14,17-triol (1)
(1S,2S,5S,10R,11S,14R,15R)-14-[(2R,5R)-5-Ethyl-6-methylheptan-2-yl]-2,15-dimethyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadecan-5-ol (1)
(1S,2S,7S,10R,15R)-2,15-dimethyl-14-(1,4,6-trihydroxy-6-methylheptan-2-yl)tetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadecane-5,9,16-triol (1)

Study type

Unknown experiment type (1)

Release Date

2021 (37)
2025 (33)
2022 (26)
2023 (21)
2024 (18)
2016 (17)
2018 (16)
2020 (15)
2017 (10)
2019 (7)
2015 (6)
2013 (6)
2014 (5)
2012 (3)
2011 (2)
2026 (1)
2010 (1)
2009 (1)
2007 (1)

Lab affiliation

Genomics Research Center, Academia Sinica, Taipei, 11529 Taiwan (2)
Sichuan university (2)
Beijing proteome research center, Beijing, China (1)
Cancer and Immunology Research Center, National Yang Ming Chiao Tung University (1)
Changhai Hospital, Naval Medical University, Shanghai, 200433, China. (1)
Department of Orthopedics, Xinqiao Hospital, Third Military Medical University (Army Medical University), Chongqing, China. (1)
Doctor at Tongji Hospital, Huazhong University of Science and Technology, Wuhan, China (1)
Institute (1)
Institute of Biomedical Sciences, Academia Sinica (1)
Kunming Institute of Zoology, Chinese Academy of Sciences (1)
State Key Laboratory of Proteomics; Beijing Proteome Research Center; National Center for Protein Sciences (Beijing) Beijing Institute of Lifeomics; China (1)
The Institute of Cancer Research (1)
UT MD Anderson Cancer Center (1)
University of Michigan Medical School, Department of Biological Chemistry, Ann Arbor, MI (1)

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Flavonoid Biosynthesis Is Likely More Susceptible to Elevation and Tree Age Than Other Branch Pathways Involved in Phenylpropanoid Biosynthesis in Ginkgo Leaves

Ginkgo leaves are always resources for flavonoids pharmaceutical industry. However, the effect of the elevation and tree age changes on flavonoid biosynthesis have not been detailly explored in Ginkgo leaves. In addition, whether these environmental pressures have similar effects on the biosynthesis...

2020-12-14 | MTBLS962 | MetaboLights

LolDF-mediated lipoprotein transport LC-MSMS in Acinetobacter

LolDF-mediated lipoprotein transport LC-MSMS in Acinetobacter, endogenous purified LolD and LolF

ORGANISM(S): Acinetobacter sp. ADP1

2026-08-04 | PXD081486 | Pride

Metabolomic fingerprinting of bull spermatozoa for identification of fertility signature metabolites

The objective of the study was to identify the fertility-associated metabolites in bovine spermatozoa using liquid chromatography-mass spectrometry (LC-MS). Six Holstein Friesian crossbred bulls (three high-fertile and three low-fertile bulls) were the experimental animals. Sperm proteins were isola...

2021-12-07 | MTBLS1071 | MetaboLights

Serum metabolomic profiles for distinguishing lung cancer from pulmonary tuberculosis: identification of rapid and noninvasive biomarker

BACKGROUND: Pulmonary tuberculosis (TB) and lung cancer (LC) have similar clinical symptoms and atypical imaging findings which are easily misdiagnosed. There is an urgent need for a noninvasive, rapid and accurate biomarker for distinguishing LC from TB.

METHODS:

2024-01-16 | MTBLS6990 | MetaboLights

A Comparative Metabolomics Study of Multiple Urological Diseases by Highly Sensitive Dansylation Isotope Labeling LC-MS.

Not available

S-EPMC12691989 | biostudies-literature

A Comparative Proteomic Analysis to Explore the Influencing Factors on Endometritis Using LC-MS/MS.

Not available

S-EPMC10298677 | biostudies-literature

Effect of Radial Shock Wave Therapy on Spasticity of the Upper Limb in Patients With Chronic Stroke: A Prospective, Randomized, Single Blind, Controlled Trial.

Not available

S-EPMC4863782 | biostudies-literature

LC-MSMS of endogenous purified lipoprotein transporter LolDF in Acinetobacter

LolDF-mediated lipoprotein transport LC-MSMS in Acinetobacter, endogenous purified LolD and LolF

ORGANISM(S): Acinetobacter sp. ADP1

2026-08-04 | PXD081527 | Pride

Lipoprotein Lc-msms Loldf Acinetobacter

Quantitative proteomics reveals middle infrared radiation-interfered networks in breast cancer cells.

Data from ProteomeXchange, PXD ID: PXD001078. File: folder summary. Published as part of J Proteome Res. 2015 Feb 6;14(2):1250-62 . From the Abstract: {{i}} ... Treatment of triple-negative breast cancer (TNBC) is complex and challenging, especially when metastasis has developed. In this study, we ...

ORGANISM(S): Homo_sapiens_viruses, Human_female

GPM32320015984 | GPMDB

Resource Reanalysis

Lung Lipidomic Alterations in Beagle Dogs Infected with Toxocara canis

Toxocariasis, mainly caused by Toxocara canis, and to a lesser extent, Toxocara cati, is a neglected parasitic zoonosis. The mechanisms that underlie the changes in lipid metabolism of T. canis infection in Beagle dogs' lungs remain unclear. Lipidomics is a rapidly emer...

2023-08-21 | MTBLS5583 | MetaboLights

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