List of Studies ( Metabolite:Acetyl-CoA)
Study_id | Analysis_id | Study_title | Source | Species | Disease | Institute | Units(range) |
---|---|---|---|---|---|---|---|
ST002497 | AN004101 | Postnatal hyperglycemia alters amino acid profile in retinas | Retina | Mouse | Eye disease | Boston Childrens Hospital | Absolute Intensity |
ST002970 | AN004879 | Untargeted metabolomics of fatty alcohol production at time 90 min of bioconversion | Bacterial cells | Bacteria | Vidyasirimedhi Institute of Science and Technology | abundance | |
ST002971 | AN004880 | Untargeted metabolomics of bioluminescent cell at T24h | Bacterial cells | Bacteria | Vidyasirimedhi Institute of Science and Technology | abundance | |
ST002972 | AN004881 | Untargeted metabolomics of alkane producing strains at time 5 h of bioconversion | Bacterial cells | Bacteria | Vidyasirimedhi Institute of Science and Technology | abundance | |
ST003104 | AN005083 | Metabolomics studies on human cardiac samples | Heart | Human | Heart disease | University of Sydney | abundance |
ST003252 | AN005328 | Metabolomics studies on mouse cardiac samples on a Western diet | Heart | Mouse | Obesity; Diabetes; Hypertension; Hyperglycemia | University of Sydney | abundance |
ST003253 | AN005331 | Metabolomics studies on mouse liver samples on a Western diet | Liver | Mouse | Obesity; Diabetes; Hypertension; Hyperglycemia | University of Sydney | abundance |
ST001680 | AN002740 | Metabolome of NAFLD in high fat diet mouse model | Liver | Mouse | Fatty liver disease | Weill Cornell Medicine | Abundance |
ST002864 | AN004696 | Metabolic profiling, glucose tracing and glutamine tracing in naive and Enzalutamide-treated 16D prostate cancer cells expressing RFP or MYC | Prostate cancer cells | Human | Cancer | University of California, Los Angeles | Abundance |
ST002865 | AN004697 | Metabolic profiling, glucose tracing and glutamine tracing in 16D prostate cancer cells treated with vehicle, AR inhibitor Enzalutamide, AR inhibitor Apalutamide, or AR degrader/PROTAC ARCC-4 | Prostate cancer cells | Human | Cancer | University of California, Los Angeles | Abundance |
ST002830 | AN004623 | L-isoleucine in P10 STZ | Retina | Mouse | Retinopathy of prematurity | Boston Childrens Hospital | abundance/intensity |
ST001822 | AN002958 | The RNA-binding protein RBP42 regulates cellular energy metabolism in mammalian-infective Trypanosoma brucei | Cultured cells | Trypanosoma brucei | Rutgers University | arbitrary | |
ST003076 | AN005034 | Data-dependent and -independent acquisition lipidomics analysis reveals the tissue-dependent effect of metformin on lipid metabolism | Adipose tissue | Mouse | North Carolina State University | arbitrary unit | |
ST003076 | AN005034 | Data-dependent and -independent acquisition lipidomics analysis reveals the tissue-dependent effect of metformin on lipid metabolism | Blood | Mouse | North Carolina State University | arbitrary unit | |
ST003076 | AN005034 | Data-dependent and -independent acquisition lipidomics analysis reveals the tissue-dependent effect of metformin on lipid metabolism | Heart | Mouse | North Carolina State University | arbitrary unit | |
ST003076 | AN005034 | Data-dependent and -independent acquisition lipidomics analysis reveals the tissue-dependent effect of metformin on lipid metabolism | Intestine | Mouse | North Carolina State University | arbitrary unit | |
ST003076 | AN005034 | Data-dependent and -independent acquisition lipidomics analysis reveals the tissue-dependent effect of metformin on lipid metabolism | Kidney | Mouse | North Carolina State University | arbitrary unit | |
ST003076 | AN005034 | Data-dependent and -independent acquisition lipidomics analysis reveals the tissue-dependent effect of metformin on lipid metabolism | Liver | Mouse | North Carolina State University | arbitrary unit | |
ST003076 | AN005034 | Data-dependent and -independent acquisition lipidomics analysis reveals the tissue-dependent effect of metformin on lipid metabolism | Muscle | Mouse | North Carolina State University | arbitrary unit | |
ST001062 | AN001736 | Arabidopsis Nit1 knockout metabolomics | Plant | Arabidopsis thaliana | University of California, Davis | Arbitrary units | |
ST003102 | AN005076 | Cellular adaptation to cancer therapy occurs by progressive state transitions along a resistance continuum | Ovarian cancer cells | Human | Cancer | NYU Langone Health | Arbitrary units |
ST002831 | AN004624 | Folate depletion upregulates heme synthesis | Cultured cells | Human | Anemia | Boston Children's Hospital, Harvard Medical School | Arbitrary Units |
ST003018 | AN004952 | Polar metabolite levels in K562 cells following PKC inhibition in 2,000 nM or 100 nM FA conditions | Cultured cells | Human | Anemia | Boston Children's Hospital, Harvard Medical School | Arbitrary Units |
ST003020 | AN004954 | Polar metabolite levels in MEL cells following PKC inhibition in 2,000 nM or 100 nM FA conditions | Cultured cells | Mouse | Anemia | Boston Children's Hospital, Harvard Medical School | Arbitrary Units |
ST001902 | AN003093 | Metabolomics analysis of AsPC-1 PDAC cells treated with Porcupine inhibitor (LGK974) | Cultured cells | Human | Cancer | University of California, Los Angeles | area |
ST002835 | AN004631 | Investigation of FGFR signaling controlled metabolism in FGFR2-fusion+ intrahepatic cholangiocarcinoma | Tumor cells | Human | Cancer | Massachusetts General Hospital | area analyzed by Compound discoverer (counts x seconds) |
ST002835 | AN004632 | Investigation of FGFR signaling controlled metabolism in FGFR2-fusion+ intrahepatic cholangiocarcinoma | Tumor cells | Human | Cancer | Massachusetts General Hospital | area analyzed by Compound discoverer (counts x seconds) |
ST003106 | AN005085 | 13C-palmitate labeling experiment in ICC13-7 treated with DMSO or Infigratinib | Cultured cells | Human | Cancer | Massachusetts General Hospital | area analyzed by Compound discoverer (counts x seconds) |
ST000172 | AN000266 | THP1 Human Monocyte cells Project A (part I) | Mononuclear cells | Human | University of Michigan | Area normalized to protein | |
ST002708 | AN004390 | Levels of central carbon metabolites in choroid plexus as part of natural diurnal variation | Brain | Mouse | Circadian Rhythm Disorder | Boston Childrens Hospital | a.u. |
ST003088 | AN005050 | Metabolome changes in embryonic CSF (Part 10) | Blood | Mouse | Autism | Boston Children's Hospital, Harvard Medical School | a.u. |
ST003088 | AN005050 | Metabolome changes in embryonic CSF (Part 10) | CSF | Mouse | Autism | Boston Children's Hospital, Harvard Medical School | a.u. |
ST003088 | AN005050 | Metabolome changes in embryonic CSF (Part 10) | Liver | Mouse | Autism | Boston Children's Hospital, Harvard Medical School | a.u. |
ST003199 | AN005249 | Metabolite profiling in the liver from fasted eIF4ES209A (S209A) mice compared to fasted wild type (WT) mice | Liver | Mouse | Cancer | University of Chicago | A.U. |
ST002123 | AN003476 | GCN2 regulates mitochondrial OXPHOS in HSPCs under proliferation conditions. | Bone marrow | Mouse | Sun Yat-sen University | AU | |
ST003123 | AN005117 | OMM1.3 uveal melanoma cells fed with [U-13C6] glucose and treated with Fasnall for 4 h | Cultured cells | Human | Cancer | Wistar Institute | AU |
ST003123 | AN005118 | OMM1.3 uveal melanoma cells fed with [U-13C6] glucose and treated with Fasnall for 4 h | Cultured cells | Human | Cancer | Wistar Institute | AU |
ST003147 | AN005163 | BT-474 cells fed with [13C2] acetate and treated with 1 uM Fasnall or 1 uM GSK2194069 for 24 h | Cultured cells | Human | Cancer | Wistar Institute | AU |
ST003147 | AN005164 | BT-474 cells fed with [13C2] acetate and treated with 1 uM Fasnall or 1 uM GSK2194069 for 24 h | Cultured cells | Human | Cancer | Wistar Institute | AU |
ST003148 | AN005165 | BT-474 cells fed with [U-13C6] D-glucose or [U-13C5] L-glutamine and treated with Fasnall and GSK2194069 for 24 h | Cultured cells | Human | Cancer | Wistar Institute | AU |
ST003152 | AN005171 | Metabolomics analysis of murine xenograft tumors derived from human breast cancer cell line MCF7 1 h after isotopic glucose bolus | Tumor cells | Mouse | Cancer | Wistar Institute | AU |
ST003152 | AN005172 | Metabolomics analysis of murine xenograft tumors derived from human breast cancer cell line MCF7 1 h after isotopic glucose bolus | Tumor cells | Mouse | Cancer | Wistar Institute | AU |
ST002374 | AN003869 | Metabolomics analysis of WT vs. GOT1 knockout CD8+ T cells | Cultured cells | Mouse | Johns Hopkins University | AUC | |
ST002375 | AN003870 | Metabolomics analysis of WT or GOT1 knockout CD8+ T cells cultured in serine-replete or serine-free media | Cultured cells | Mouse | Johns Hopkins University | AUC | |
ST002914 | AN004784 | Untangling the Dynamics of Lysine Acetylation and Phosphorylation in Adipogenesis in the Established Human and Mouse Adipocyte Cell Lines SGBS and 3T3L1 | Adipose tissue | Human | Obesity | Helmholtz Centre for Environmental Research | AUC |
ST001074 | AN001756 | Open source discovery of starting points for next generation chemoprotective antimalarial drugs (Biofocus 1) | Parasite | Human | Pennsylvania State University | Average Peak Area | |
ST002457 | AN004009 | Mouse kidney metabolomics (Whole kidney) | Kidney | Mouse | Chronic kidney disease | Hadassah Medical Center | concentration |
ST002925 | AN004796 | Metabolite analysis of hepatic Pptc7-ko mice under fed or fasting conditions | Liver | Mouse | National Institute of Biological Sciences, Beijing | count | |
ST003060 | AN005015 | Fluxomics of hormone deprivation in ER+ breast cancer cell lines | Breast cancer cells | Human | Cancer | Dartmouth College | counts |
ST000755 | AN001330 | Rat Retinal Detachment Metabolomics Timecourse (part II) | Eye tissue | Rat | University of Michigan | Counts | |
ST002869 | AN004702 | Identifying Biodegradation Pathways of Cetrimonium Bromide (CTAB) Using Metagenome, Metatranscriptome, and Metabolome Tri-omics Integration | Water | Bacteria | Environmental exposure | Arizona State University | counts per second |
ST003365 | AN005514 | Intracellular and medium metabolomics for BT-474 breast cancer cells treated with a range of Fasnall and GSK2194069 concentrations for 24 h | Cultured cells | Human | Cancer | Wistar Institute | Counts per second (cps) |
ST003365 | AN005515 | Intracellular and medium metabolomics for BT-474 breast cancer cells treated with a range of Fasnall and GSK2194069 concentrations for 24 h | Cultured cells | Human | Cancer | Wistar Institute | Counts per second (cps) |
ST003366 | AN005516 | Malate dehydrogenase (MDH) inhibition assay: Fasnall does not affect MDH activity in vitro | Synthetic | Other | Cancer | Wistar Institute | Counts per second (cps) |
ST003366 | AN005517 | Malate dehydrogenase (MDH) inhibition assay: Fasnall does not affect MDH activity in vitro | Synthetic | Other | Cancer | Wistar Institute | Counts per second (cps) |
ST003367 | AN005518 | Intracellular and medium metabolomics for BT-474 cells treated with a range of C75 concentrations for 24 h | Cultured cells | Human | Cancer | Wistar Institute | Counts per second (cps) |
ST003367 | AN005519 | Intracellular and medium metabolomics for BT-474 cells treated with a range of C75 concentrations for 24 h | Cultured cells | Human | Cancer | Wistar Institute | Counts per second (cps) |
ST003411 | AN005602 | Intracellular and medium metabolomics for BT-474 cells treated with a range of C75 concentrations for 24 h (C75 MRM included) | Cultured cells | Human | Cancer | Wistar Institute | Counts per second (cps) |
ST003411 | AN005603 | Intracellular and medium metabolomics for BT-474 cells treated with a range of C75 concentrations for 24 h (C75 MRM included) | Cultured cells | Human | Cancer | Wistar Institute | Counts per second (cps) |
ST003412 | AN005604 | Intracellular and medium metabolomics for BT-474 cells treated with cerulenin, TVB-2640, and TVB-3166 for 24 h | Cultured cells | Human | Cancer | Wistar Institute | Counts per second (cps) |
ST003412 | AN005605 | Intracellular and medium metabolomics for BT-474 cells treated with cerulenin, TVB-2640, and TVB-3166 for 24 h | Cultured cells | Human | Cancer | Wistar Institute | Counts per second (cps) |
ST003427 | AN005627 | Intracellular and medium metabolomics of BT-474 cells treated with dimethylmalonate | Breast cancer cells | Human | Cancer | Wistar Institute | Counts per second (cps) |
ST003427 | AN005628 | Intracellular and medium metabolomics of BT-474 cells treated with dimethylmalonate | Breast cancer cells | Human | Cancer | Wistar Institute | Counts per second (cps) |
ST003428 | AN005629 | Intracellular and medium metabolomics of BT-474 cells treated with rotenone | Cultured cells | Human | Cancer | Wistar Institute | Counts per second (cps) |
ST003428 | AN005630 | Intracellular and medium metabolomics of BT-474 cells treated with rotenone | Cultured cells | Human | Cancer | Wistar Institute | Counts per second (cps) |
ST003429 | AN005631 | Intracellular and medium metabolomics of BT-474 cells treated with Fasnall that was manufactured by Enamine | Cultured cells | Human | Cancer | Wistar Institute | Counts per second (cps) |
ST003429 | AN005632 | Intracellular and medium metabolomics of BT-474 cells treated with Fasnall that was manufactured by Enamine | Cultured cells | Human | Cancer | Wistar Institute | Counts per second (cps) |
ST003430 | AN005633 | Intracellular and medium metabolomics of BT-474 cells treated with GSK2194069 | Cultured cells | Human | Cancer | Wistar Institute | Counts per second (cps) |
ST003430 | AN005634 | Intracellular and medium metabolomics of BT-474 cells treated with GSK2194069 | Cultured cells | Human | Cancer | Wistar Institute | Counts per second (cps) |
ST003431 | AN005635 | Metabolomics analysis of breast cancer cell lines treated with dimethylmalonate (DMM), GSK2194069, and their combination. | Cultured cells | Human | Cancer | Wistar Institute | Counts per second (cps) |
ST003431 | AN005636 | Metabolomics analysis of breast cancer cell lines treated with dimethylmalonate (DMM), GSK2194069, and their combination. | Cultured cells | Human | Cancer | Wistar Institute | Counts per second (cps) |
ST003432 | AN005637 | Intracellular and medium metabolomics of BT-474 cells treated with LW6 | Cultured cells | Human | Cancer | Wistar Institute | Counts per second (cps) |
ST003432 | AN005638 | Intracellular and medium metabolomics of BT-474 cells treated with LW6 | Cultured cells | Human | Cancer | Wistar Institute | Counts per second (cps) |
ST003433 | AN005639 | Intracellular and medium metabolomics of BT-474 cells treated with dimethylmalonate, Fasnall, and GSK2194069 | Cultured cells | Human | Cancer | Wistar Institute | Counts per second (cps) |
ST003433 | AN005640 | Intracellular and medium metabolomics of BT-474 cells treated with dimethylmalonate, Fasnall, and GSK2194069 | Cultured cells | Human | Cancer | Wistar Institute | Counts per second (cps) |
ST003434 | AN005641 | Plasma concentrations of Fasnall in mice after a bolus of 10 mg/kg administered intraperitoneally. | Blood | Human | Cancer | Wistar Institute | Counts per second (cps) |
ST003434 | AN005642 | Plasma concentrations of Fasnall in mice after a bolus of 10 mg/kg administered intraperitoneally. | Blood | Human | Cancer | Wistar Institute | Counts per second (cps) |
ST003435 | AN005643 | Metabolomics analysis of zebrafish embryos treated with rotenone, Fasnall, TVB-2640, and GSK2194069 | Media, Metabolite extract | Zebra fish | Cancer | Wistar Institute | Counts per second (cps) |
ST003435 | AN005644 | Metabolomics analysis of zebrafish embryos treated with rotenone, Fasnall, TVB-2640, and GSK2194069 | Media, Metabolite extract | Zebra fish | Cancer | Wistar Institute | Counts per second (cps) |
ST003436 | AN005645 | Pharmacokinetics of Fasnall in NSG mice | Brain, Heart, Liver, Blood | Mouse | Cancer | Wistar Institute | Counts per second (cps) |
ST003436 | AN005646 | Pharmacokinetics of Fasnall in NSG mice | Brain, Heart, Liver, Blood | Mouse | Cancer | Wistar Institute | Counts per second (cps) |
ST000832 | AN001840 | Rat Retinal Detachment Metabolomics Timecourse | Eye tissue | Rat | University of Michigan | counts/ug protein | |
ST002187 | AN003581 | Interplay of CodY and CcpA in regulating central metabolism and biofilm formation in S. aureus | Bacterial cells | S. aureus | Bacterial infection | University of Nebraska Medical Center | CPS |
ST002567 | AN004228 | Metabolomics of Human islets treated with DHT and high-glucose challenge | Pancreas | Human | Diabetes | Tulane University School of Medicine | EicCoreArea/Peak Area |
ST002323 | AN003792 | SETD1A regulates transcriptional pause release of heme biosynthesis genes in leukemia | Cultured cells | Human | Cancer | Chiba University | fmol/cell |
ST001238 | AN002056 | P falciparum asexual metabolomics following drug treatment (part-I) | Plasmodium cells | Plasmodium falciparum | Malaria | Pennsylvania State University | Fold change versus untreated |
ST002327 | AN003796 | Effect of PARK7 gene KO on midbrain organoids | Cultured cells | Human | Icahn School of Medicine at Mount Sinai | intensity | |
ST001788 | AN002899 | β-Adrenergic regulation of metabolism in macrophages (part-IV) | Macrophages | Human | Monash University | Intensity | |
ST002813 | AN004576 | Effects of acute cold exposure on mouse metabolome | BAT | Mouse | University of Pennsylvania | Intensity | |
ST002813 | AN004576 | Effects of acute cold exposure on mouse metabolome | Blood | Mouse | University of Pennsylvania | Intensity | |
ST002813 | AN004576 | Effects of acute cold exposure on mouse metabolome | Diaphragm | Mouse | University of Pennsylvania | Intensity | |
ST002813 | AN004576 | Effects of acute cold exposure on mouse metabolome | gWAT | Mouse | University of Pennsylvania | Intensity | |
ST002813 | AN004576 | Effects of acute cold exposure on mouse metabolome | Heart | Mouse | University of Pennsylvania | Intensity | |
ST002813 | AN004576 | Effects of acute cold exposure on mouse metabolome | Liver | Mouse | University of Pennsylvania | Intensity | |
ST002813 | AN004576 | Effects of acute cold exposure on mouse metabolome | Quadriceps | Mouse | University of Pennsylvania | Intensity | |
ST003283 | AN005378 | Systematic evaluation of the hepatic de novo lipogenic substrate supply network reveals a hierarchical mitochondrial-cytosolic control structure | Liver | Mouse | Metabolic disease | University of Iowa | Intensity |
ST001188 | AN001980 | P. falciparum infected erythrocytes | Cultured cells | Plasmodium falciparum | Malaria | University of Melbourne | ion count |
ST001860 | AN003016 | Spontaneous hydrolysis and spurious metabolic properties of α-ketoglutarate esters | Cultured cells | Human | University of British Columbia | ion counts | |
ST002119 | AN003469 | Metabolomics analysis of zebrafish response to CID661578 treatment | Larvae | Zebrafish | Diabetes | North Carolina State University | ion counts |
ST002152 | AN003525 | Metabolomics analysis of mouse liver with or without SIRT5 deficiency | Liver | Mouse | North Carolina State University | ion counts | |
ST000441 | AN000692 | Metabolomic Profiling of the Malaria Box Reveals Antimalarial Target Pathways | Plasmodium cells | Plasmodium falciparum | Malaria | Pennsylvania State University | log2 fold change vs untreated |
ST003405 | AN005588 | Specific activation of the integrated stress response uncovers regulation of central carbon metabolism and lipid droplet biogenesis | Cultured cells | Human | Cancer | Calico Life Sciences | log2 peak area top |
ST002822 | AN004601 | Effect of ERR Agonist in Mouse Heart Post Pressure Overload | Heart | Mouse | Baylor College of Medicine | log transformed data | |
ST000162 | AN000254 | Yeast glycolysis in normoxia and hypoxia (150121_pkf2) | Yeast cells | Yeast | University of Michigan | mM | |
ST000170 | AN000447 | 13C mass isotopomer analysis (LCMS flux studies) MLL-AF9 (part III) | Cells | Mouse | Baylor College of Medicine | mM | |
ST002477 | AN004046 | Neutrophil metabolomics in COVID-19 | Neutrophils | Human | COVID-19 | UT Southwestern Medical Center | MS reading |
ST003027 | AN004962 | NMR- and MS-based omics reveal characteristic metabolome atlas and optimize biofluid earlydiagnostic biomarkers for esophageal squamous cell carcinoma (part-Ⅳ) | Tissue | Human | Cancer | Radiology Department, Second Affiliated Hospital, Shantou University Medical College, Shantou | m/z |
ST002174 | AN003562 | Identifying a tryptophan derivative in hydrogen peroxide-treated cell culture medium | Media | Abiotic | NYU Langone Health | N/L | |
ST000570 | AN000877 | Metabolome analysis of the cecal contents of GF mice and GF mice colonized with dominant gut microbes present in the ceca of neonatal and adult mice | Feces | Mouse | Keio University | nmol/g | |
ST001300 | AN002165 | Luminal metabolome profiles ofUC-HMA mice transplanted with a healthy human-derived fecal microbiota (FMT). | Feces | Mouse | Bacterial infection | University of Michigan | nmol/g |
ST001301 | AN002167 | Luminal metabolome profiles of human microbiota-associated (HMA) mice treated with anti-IL-22 antibody or control antibody | Feces | Mouse | Bacterial infection | University of Michigan | nmol/g |
ST001961 | AN003196 | Metabolomics of brown adipose tissue in murine heart failure model | Adipose tissue | Mouse | Juntendo University | nmol/g | |
ST002172 | AN003560 | Cecal metabolome of gnotobiotic (containing a 14-member synthetic human gut microbiota), and germ-free mice fed with two distinct rodent diets with varying fiber content. | Cecum | Mouse | Luxembourg Institute of Health | nmol/g | |
ST002476 | AN004078 | High body temperature increases gut microbiota-dependent host resistance to influenza A virus and SARS-CoV-2 infection (Mouse) | Intestine | Mouse | COVID-19 | Keio University | nmol/g |
ST002476 | AN004078 | High body temperature increases gut microbiota-dependent host resistance to influenza A virus and SARS-CoV-2 infection (Mouse) | Intestine | Mouse | Influenza | Keio University | nmol/g |
ST002479 | AN004080 | High body temperature increases gut microbiota-dependent host resistance to influenza A virus and SARS-CoV-2 infection (Hamster) | Intestine | Mouse | COVID-19 | Keio University | nmol/g |
ST002479 | AN004080 | High body temperature increases gut microbiota-dependent host resistance to influenza A virus and SARS-CoV-2 infection (Hamster) | Intestine | Mouse | Influenza | Keio University | nmol/g |
ST001136 | AN001862 | Metabolme analysis of OPC-163493 on the Liver of ZDF rats (part-II) | Liver | Rat | Diabetes | Otsuka Pharmaceuticals | nmol/g tissue |
ST000351 | AN000571 | Determining the metabolic profile of wildtype, lrgAB, and atlA mutant Steptococcus mutans grown aerobically and anaerobically | Bacterial cells | Streptococcus | Antibiotic resistance | University of Florida | nmol/mg |
ST001350 | AN002246 | Extraction of high-resolution Metabolomics data of the Yeast Metabolic Cycle | Yeast cells | Yeast | University of Florida | nmol/mg protein | |
ST001376 | AN002296 | 2,3,7,8 -Tetrachlorodibenzo-p-dioxin Mediated Effects on Hepatic Coenzyme A (CoA) and Acetyl-CoA Levels | Liver | Mouse | Michigan State University | nmol/mg total protein | |
ST001779 | AN002889 | Untargeted Metabolomics analysis of A549 treated with 0.5 mM extracellular ATP and 10 ng/ml TGF-beta | Lung | Human | Cancer | Ohio University | normalized |
ST001610 | AN002644 | Control (DMSO 0.1%; v/v) and 10 µM DRB18 treated A549 lung cancer cells in vitro for 48 hours | Lung | Human | Cancer | Ohio University | Normalized abundances |
ST001660 | AN002711 | Plasmodium falciparum metabolomics as a result of treatment with putative acetyl-CoA synthetase inhibitors | Cultured cells | Fungi | Malaria | Pennsylvania State University | Normalized and blank subtracted peak area |
ST001660 | AN002711 | Plasmodium falciparum metabolomics as a result of treatment with putative acetyl-CoA synthetase inhibitors | Cultured cells | Plasmodium falciparum | Malaria | Pennsylvania State University | Normalized and blank subtracted peak area |
ST002969 | AN004878 | Polar metabolites in cecal tissue of mice treated with or without ampicillin and tributyrin | Cecum | Mouse | Bacterial infection | The Rockefeller University | Normalized Area |
ST002160 | AN003539 | Global metabolomics analysis of neutrophils isolated from tumor | Tumor cells | Mouse | Cancer | The Wistar Institute | Normalized MS Peak Area |
ST002809 | AN004568 | Role of cilia in mitochondrial function | Cultured cells | Dog | Kidney disease | Medical University of South Carolina | Normalized/scaled raw area counts |
ST002809 | AN004568 | Role of cilia in mitochondrial function | Cultured cells | Mouse | Kidney disease | Medical University of South Carolina | Normalized/scaled raw area counts |
ST001985 | AN003236 | Profiling Plasmodium falciparum parasites and human red blood cells after treatment with MMV693183 | Blood | Human | Malaria | Pennsylvania State University | Peak Abundance (normalized, blank subtracted, and corrected for baseline noise) |
ST001985 | AN003236 | Profiling Plasmodium falciparum parasites and human red blood cells after treatment with MMV693183 | Blood | Plasmodium falciparum | Malaria | Pennsylvania State University | Peak Abundance (normalized, blank subtracted, and corrected for baseline noise) |
ST001985 | AN003236 | Profiling Plasmodium falciparum parasites and human red blood cells after treatment with MMV693183 | Cultured cells | Human | Malaria | Pennsylvania State University | Peak Abundance (normalized, blank subtracted, and corrected for baseline noise) |
ST001985 | AN003236 | Profiling Plasmodium falciparum parasites and human red blood cells after treatment with MMV693183 | Cultured cells | Plasmodium falciparum | Malaria | Pennsylvania State University | Peak Abundance (normalized, blank subtracted, and corrected for baseline noise) |
ST002024 | AN003294 | Plasmodium falciparum stable-isotope carbon labeling to explore metabolic consequences of keto–acid dehydrogenase disruption | Cultured cells | Plasmodium falciparum | Malaria | Pennsylvania State University | Peak Abundance (normalized, blank subtracted, and corrected for baseline noise) |
ST002011 | AN003277 | The anticancer human mTOR inhibitor MLN0128/Sapanisertib with potent multistage in vitro antiplasmodium activity and in vivo antimalarial efficacy in a humanised mouse model is an inhibitor of multiple Plasmodium falciparum kinases. | Blood | Plasmodium falciparum | Malaria | Pennsylvania State University | peak area |
ST002011 | AN003278 | The anticancer human mTOR inhibitor MLN0128/Sapanisertib with potent multistage in vitro antiplasmodium activity and in vivo antimalarial efficacy in a humanised mouse model is an inhibitor of multiple Plasmodium falciparum kinases. | Blood | Plasmodium falciparum | Malaria | Pennsylvania State University | peak area |
ST002078 | AN003387 | Multiple modes of interfering with the activity of Plasmodium falciparum cytoplasmic isoleucyl-tRNA synthetase illustrate the enzyme is a promising antimalarial target. | Cultured cells | Plasmodium falciparum | Malaria | Pennsylvania State University | peak area |
ST002078 | AN003388 | Multiple modes of interfering with the activity of Plasmodium falciparum cytoplasmic isoleucyl-tRNA synthetase illustrate the enzyme is a promising antimalarial target. | Cultured cells | Plasmodium falciparum | Malaria | Pennsylvania State University | peak area |
ST002078 | AN003389 | Multiple modes of interfering with the activity of Plasmodium falciparum cytoplasmic isoleucyl-tRNA synthetase illustrate the enzyme is a promising antimalarial target. | Cultured cells | Plasmodium falciparum | Malaria | Pennsylvania State University | peak area |
ST002078 | AN003390 | Multiple modes of interfering with the activity of Plasmodium falciparum cytoplasmic isoleucyl-tRNA synthetase illustrate the enzyme is a promising antimalarial target. | Cultured cells | Plasmodium falciparum | Malaria | Pennsylvania State University | peak area |
ST002184 | AN003577 | Metabolic effect of the loss of mitochondrial-specific aspartyl-tRNA synthetase Das2 on mouse intestinal epithelial cells | Intestine | Mouse | CECAD Research Center | peak area | |
ST002199 | AN003599 | FOXA2 controls the anti-oxidant response in FH-deficient cells independent of NRF2 | Cultured cells | Mouse | Cancer | CECAD Research Center | peak area |
ST002205 | AN003608 | Effect of Hira loss in the metabolic landscape of Fh1-deficient cells | Cultured cells | Mouse | Cancer | CECAD Research Center, University Hospital Cologne | peak area |
ST002218 | AN003627 | Effect of Hira loss in the metabolic landscape of Fh1-deficient cells Part 2 | Cultured cells | Mouse | Cancer | CECAD Research Center | peak area |
ST002221 | AN003630 | Glutaminolysis contribution to the carbon backbone of aspartate through ATP Citrate Lyase (ACLY) in ccRCC | Cultured cells | Human | Cancer | CECAD Research Center | peak area |
ST002222 | AN003631 | Glutaminolysis contribution to the carbon backbone of aspartate and glutamate in ccRCC | Cultured cells | Human | Cancer | CECAD Research Center | peak area |
ST002223 | AN003632 | Metabolic profiling of mouse tissues and tissue interstitial fluids | Heart | Mouse | Cancer | CECAD Research Center | peak area |
ST002223 | AN003632 | Metabolic profiling of mouse tissues and tissue interstitial fluids | Kidney | Mouse | Cancer | CECAD Research Center | peak area |
ST002223 | AN003632 | Metabolic profiling of mouse tissues and tissue interstitial fluids | Liver | Mouse | Cancer | CECAD Research Center | peak area |
ST002223 | AN003632 | Metabolic profiling of mouse tissues and tissue interstitial fluids | Lung | Mouse | Cancer | CECAD Research Center | peak area |
ST002224 | AN003633 | Intracellular metabolic profile of renal cells cultured in Plasmax | Cultured cells | Human | Cancer | CECAD Research Center | peak area |
ST002242 | AN003660 | Hypoxia promotes osteogenesis via regulating the acetyl-CoA-mediated mito-nuclear communication. | Cultured cells | Mouse | CECAD Research Center | peak area | |
ST002431 | AN003957 | MS profiling of the Long Term Evolution Experiment | Bacterial cells | E. coli | Rutgers University | peak area | |
ST002431 | AN003958 | MS profiling of the Long Term Evolution Experiment | Bacterial cells | E. coli | Rutgers University | peak area | |
ST002635 | AN004307 | MoTrPAC: Endurance exercise training study in young adult rats, Rat Hippocampus Powder - Untargeted Ion-Pair Negative | Hippocampus | Rat | University of Michigan | peak area | |
ST002643 | AN004315 | MoTrPAC: Endurance exercise training study in young adult rats, Rat Gastrocnemius Powder - Untargeted Ion-Pair Negative | Gastrocnemius | Rat | University of Michigan | peak area | |
ST002650 | AN004322 | MoTrPAC: Endurance exercise training study in young adult rats, Rat Heart Powder - Untargeted Ion-Pair Negative | Heart | Rat | University of Michigan | peak area | |
ST002655 | AN004327 | MoTrPAC: Endurance exercise training study in young adult rats, Rat Kidney Powder - Untargeted Ion-Pair Negative | Kidney | Rat | University of Michigan | peak area | |
ST002669 | AN004341 | MoTrPAC: Endurance exercise training study in young adult rats, Rat Lung Powder - Untargeted Ion-Pair Negative | Lung | Rat | University of Michigan | peak area | |
ST002676 | AN004348 | MoTrPAC: Endurance exercise training study in young adult rats, Rat Liver Powder - Untargeted Ion-Pair Negative | Liver | Rat | University of Michigan | peak area | |
ST002683 | AN004356 | MoTrPAC: Endurance exercise training study in young adult rats, Rat Brown Adipose Powder - Untargeted Ion-Pair Negative | Brown adipose | Rat | University of Michigan | peak area | |
ST002689 | AN004362 | MoTrPAC: Endurance exercise training study in young adult rats, Rat White Adipose Powder - Untargeted Ion-Pair Negative | White adipose | Rat | University of Michigan | peak area | |
ST002736 | AN004438 | Assessing mitochondrial bioenergetics in coronary artery disease: A translational multiomic tissue study in humans (The AMBITION study). | Heart | Human | Cardiovascular disease | Imperial College London | peak area |
ST002895 | AN004754 | Polar metabolite levels in K562 cells following folate depletion and inosine supplementation | Cultured cells | Human | Anemia | Boston Children's Hospital, Harvard Medical School | peak area |
ST002896 | AN004755 | Polar metabolite levels in MEL cells following folate depletion and inosine supplementation | Cultured cells | Mouse | Anemia | Boston Children's Hospital, Harvard Medical School | peak area |
ST002897 | AN004756 | Polar metabolite levels in K562 cells following folate depletion, SHIN1 or AICAR treatment | Cultured cells | Human | Anemia | Boston Children's Hospital, Harvard Medical School | peak area |
ST002898 | AN004757 | Polar metabolite levels in MEL cells following folate depletion, SHIN1 or AICAR treatment | Cultured cells | Mouse | Anemia | Boston Children's Hospital, Harvard Medical School | peak area |
ST002899 | AN004758 | Polar metabolite levels in erythroid progenitor cells following SHIN1 and inosine treatment | Cultured cells | Mouse | Anemia | Boston Children's Hospital, Harvard Medical School | peak area |
ST002906 | AN004769 | Polar metabolite levels in K562 cells following short-term folate depletion | Cultured cells | Human | Anemia | Boston Children's Hospital, Harvard Medical School | peak area |
ST002912 | AN004782 | Polar metabolite levels in MEL cells following folate depletion | Cultured cells | Mouse | Anemia | Boston Children's Hospital, Harvard Medical School | peak area |
ST002913 | AN004783 | Polar metabolite levels in K562 cells following folate depletion | Cultured cells | Human | Anemia | Boston Children's Hospital, Harvard Medical School | peak area |
ST003499 | AN005743 | Metabolic analysis of ADSL deficiency patients' EBV-LCLs. | Blood | Human | Mitochondrial Dysfunction | Catholic University of the Sacred Heart | peak area |
ST003499 | AN005744 | Metabolic analysis of ADSL deficiency patients' EBV-LCLs. | Blood | Human | Mitochondrial Dysfunction | Catholic University of the Sacred Heart | peak area |
ST000144 | AN000228 | Primary T Cell Baseline (Donor 5) - II | T-cells | Human | Cancer | University of Michigan | Peak area |
ST000145 | AN000230 | Primary T Cell Noxa Knockdown (Donor 8) | T-cells | Human | Cancer | University of Michigan | Peak area |
ST000146 | AN000232 | Noxa regulation of malate aspartate shuttle | T-cells | Human | Cancer | University of Michigan | Peak area |
ST000147 | AN000233 | 13C targeted metabolomics | T-cells | Human | University of Michigan | Peak area | |
ST000154 | AN000245 | Use of Aspartate Dehydrogenase by cancer cells | T-cells | Human | University of Michigan | Peak area | |
ST000157 | AN000448 | 13C mass isotopomer analysis (LCMS flux studies) MLL-AF9 (part II) | Cultured cells | Mouse | Baylor College of Medicine | Peak area | |
ST000159 | AN000251 | U13C-Glutamine and U13C-Glucose Flux Analysis (MFA SiHa B16F10) | Cultured cells | Human | University of Michigan | Peak area | |
ST000181 | AN000279 | T cell metabolism during graft-versus-host disease(CAB 311) | T-cells | Mouse | University of Michigan | Peak area | |
ST000215 | AN000317 | Liver and Plasma metaboites for 13C-glucose load in wild type, LIRKO GTT 1 mice | Liver | Mouse | University of Michigan | Peak area | |
ST000230 | AN000343 | Comprehensive analysis of transcriptome and metabolome in Intrahepatic Cholangiocarcinoma and Hepatocellular Carcinoma | Liver | Human | Cancer | Osaka City University | Peak area |
ST000260 | AN000414 | Analysis of DJ-1 Knockout Mouse Brains | Brain | Mouse | National Insitute on Aging | Peak area | |
ST000271 | AN000434 | C13 Pyruvate Flux in 3t3 L1 | Cells | Mouse | University of Michigan | Peak area | |
ST000282 | AN000449 | Pilot Study 13C flux effects when RhoC or RhoA perturbed (13C BCs) | Cells | Human | University of Michigan | Peak area | |
ST000301 | AN000479 | GBM Cell Lines Reproducibility Pilot Study | Glioma cells | Human | University of Michigan | Peak area | |
ST000302 | AN000480 | Isocitrate dehydrogenase-1/Glioma Fluxomics Study | Glioma cells | Human | University of Michigan | Peak area | |
ST001057 | AN001726 | Metabolite Extractions from Cyanobacteria | Bacterial cells | Synechococcus | Indian Institute of Technology-Bombay | Peak area | |
ST001080 | AN001763 | Dynamic labeling of intracellular metabolites in PCC 7002 | Bacterial cells | Synechococcus | Indian Institute of Technology, Bombay | Peak area | |
ST001232 | AN002050 | Combining stage - specificity and metabolomic profiling to advance drug discovery for malaria | Cultured cells | Plasmodium falciparum | Malaria | Pennsylvania State University | Peak area |
ST001279 | AN002120 | K13 mutations driving artemisinin resistance rewrite Plasmodium falciparum’s programmed intra-erythrocytic development and transform mitochondrial physiology | Parasite | Plasmodium falciparum | Malaria | Penn State | Peak area |
ST001384 | AN002309 | Plasmodium falciparum increased time in circulation underlies persistent asymptomatic infection in the dry season | Blood | Human | Malaria | Penn State | Peak area |
ST001441 | AN002409 | Metabolomics of patient-derived fibroblasts | Fibroblast cells | Human | Mitochondrial disease | North Carolina State University | Peak area |
ST001507 | AN002498 | Hepatic [U-13C]Lactate tracing and metabolomics in young and old WT and SIRT6 overexpressing mice | Liver | Mouse | Bar Ilan University | Peak area | |
ST001508 | AN002499 | Liver metabolomics in old liver-specific SIRT6 overexpressing mice | Liver | Mouse | Bar Ilan University | Peak area | |
ST001611 | AN002645 | Mouse model of sarcoma (STS) to characterize tumor vulnerabilities and identify novel targets for anti-cancer treatment | Muscle | Mouse | Cancer | North Carolina State University | Peak area |
ST001611 | AN002645 | Mouse model of sarcoma (STS) to characterize tumor vulnerabilities and identify novel targets for anti-cancer treatment | Sarcoma | Mouse | Cancer | North Carolina State University | Peak area |
ST001709 | AN002784 | SARS-CoV-2 infection rewires host cell metabolism and is potentially susceptible to mTORC1 inhibition | Cultured cells | Human | COVID-19 | University of California, Los Angeles | Peak area |
ST002376 | AN003872 | Hepatic Phosphatidylcholine Catabolism Driven by PNPLA7 and PNPLA8 Supplies Endogenous Choline to Replenish the Methionine Cycle with Methyl Groups(Pnpla8-knockout) | Liver | Mouse | Tokyo Metropolitan Institute of Medical Science | Peak area | |
ST002505 | AN004126 | A Mammalian Conserved Circular RNA CircLARP2 Regulates Hepatocellular Carcinoma Metastasis and Lipid Metabolism (Part 1) | Cultured cells | Human | Cancer | University of Science and Technology of China | Peak area |
ST002505 | AN004127 | A Mammalian Conserved Circular RNA CircLARP2 Regulates Hepatocellular Carcinoma Metastasis and Lipid Metabolism (Part 1) | Cultured cells | Human | Cancer | University of Science and Technology of China | Peak area |
ST002506 | AN004128 | Natural abundance of isotopic metabolite detection in mouse eye orgnaoids. | Retina | Mouse | Northwestern University | Peak area | |
ST002507 | AN004129 | Time-course analysis of C13 labeling in mouse eye organoids. | Retina | Mouse | Northwestern University | Peak area | |
ST002508 | AN004130 | 13C-isotopic labeling of mouse eye organoids under three conditions. | Retina | Mouse | Northwestern University | Peak area | |
ST002846 | AN004664 | Apolipoprotein E suppresses hyperlipidemia-driven hematopoiesis & inflammation by controlling mitochondrial metabolism | Macrophages | Mouse | Hyperlipidemia | Northwestern University | Peak area |
ST001954 | AN003179 | A pathogenic role for histone H3 copper reductase activity in a yeast model of Friedreich’s Ataxia | Yeast cells | Yeast | Friedreichs Ataxia | University of California, Los Angeles | Peak Area |
ST002709 | AN004391 | FH variant pathogenicity promotes purine salvage pathway dependence in kidney cancer | Cultured cells | Other | Cancer | University of California, Los Angeles | Peak Area |
ST002814 | AN004706 | Atlas of fetal metabolism during mid-to-late gestation and diabetic pregnancy | Embryonic cells | Mouse | Diabetes | University of California, Los Angeles | Peak Area |
ST002814 | AN004706 | Atlas of fetal metabolism during mid-to-late gestation and diabetic pregnancy | Embryonic cells | Mouse | Hypoglycemia | University of California, Los Angeles | Peak Area |
ST002814 | AN004706 | Atlas of fetal metabolism during mid-to-late gestation and diabetic pregnancy | Embryonic cells | Mouse | Hypoglycemia; Diabetes | University of California, Los Angeles | Peak Area |
ST002852 | AN004673 | MYC is a regulator of androgen receptor inhibition-induced metabolic requirements in prostate cancer | Prostate | Mouse | Cancer | University of California, Los Angeles | Peak Area |
ST002878 | AN004716 | Atlas of fetal metabolism during mid-to-late gestation and diabetic pregnancy. Dynamic Labelling experiment. | Embryonic cells | Mouse | Diabetes | University of California, Los Angeles | Peak Area |
ST003111 | AN005095 | Inhibition of Asparagine Synthetase Effectively Retards Polycystic Kidney Disease Progression, investigated with targeted metabolomics in Tam-Cre;Pkd1ΔC/flox mouse model kidneys. | Kidney | Mouse | Kidney disease | San Raffaele University | Peak Area |
ST000308 | AN000488 | 13C mass isotopomer analysis (LCMS flux studies) MLL-AF9 (part I) | Cells | Mouse | University of Michigan | Peak area normalized | |
ST001170 | AN001935 | Timecourse on MCF-7 cells treated with different concentration of doxorubicin | Cultured cells | Human | China Pharmaceutical University | Peak area normalized | |
ST000121 | AN000203 | Impact of anesthesia and euthanasia on metabolomics of mammalian tissues: studies in a C57BL/6J mouse model | Adipose tissue | Mouse | University of Michigan | Peak area (normalized to tissue mass) | |
ST000121 | AN000203 | Impact of anesthesia and euthanasia on metabolomics of mammalian tissues: studies in a C57BL/6J mouse model | Blood | Mouse | University of Michigan | Peak area (normalized to tissue mass) | |
ST000121 | AN000203 | Impact of anesthesia and euthanasia on metabolomics of mammalian tissues: studies in a C57BL/6J mouse model | Heart | Mouse | University of Michigan | Peak area (normalized to tissue mass) | |
ST000121 | AN000203 | Impact of anesthesia and euthanasia on metabolomics of mammalian tissues: studies in a C57BL/6J mouse model | Liver | Mouse | University of Michigan | Peak area (normalized to tissue mass) | |
ST000121 | AN000203 | Impact of anesthesia and euthanasia on metabolomics of mammalian tissues: studies in a C57BL/6J mouse model | Muscle | Mouse | University of Michigan | Peak area (normalized to tissue mass) | |
ST001149 | AN001896 | Plasmodium Niemann-Pick Type C1-Related Protein is a Druggable Target Required for Parasite Membrane Homeostasis | Cultured cells | Plasmodium falciparum | Malaria | Pennsylvania State University | Peak Area Post-Blank Subtraction |
ST001180 | AN001958 | Metabolome Profiling of Synechococcus elogatus PCC 11802 | Cultured cells | Synechococcus elongatus | Indian Institute of Technology, Bombay | Peak area ratio | |
ST001298 | AN002162 | Metabolome Profiling of Synechococcus elongatus PCC 11801 strains engineered for Succinate Production | Bacterial cells | Synechococcus elongatus | Indian Institute of Technology Bombay (IIT Bombay) | Peak area ratio | |
ST001302 | AN002168 | Metabolome Profiling of a Fast-growing Cyanobacterium Synechococcus elongatus PCC 11801 under Diurnal Cycle | Bacterial cells | Synechococcus | Indian Institute of Technology Bombay | Peak area ratio | |
ST003340 | AN005474 | Effect of feeding and the mTORC1 activity on metabolism in Caenorhabditis elegans | Worm | Roundworm | Hiroshima University | peak areas | |
ST002115 | AN003513 | LC-MS analysis of metabolic changes induced by GPX4 inhibitor treatment in cultured HT1080 cells | Cultured cells | Human | University of Texas MD Anderson Cancer Center | Peak area (top) | |
ST002919 | AN004789 | Short-term metabolic insulin response of DINCH- and MINCH-treated cells | Adipose tissue | Human | Obesity | Helmholtz Centre for Environmental Research | Peak AUC |
ST002920 | AN004790 | Possible PPARG-independent effects of DINCH and MINCH on central carbon metabolism | Adipose tissue | Human | Obesity | Helmholtz Centre for Environmental Research | Peak AUC |
ST002922 | AN004792 | Effects of DINCH and MINCH on adipocyte metabolism of human SGBS cells. | Adipose tissue | Human | Obesity | Helmholtz Centre for Environmental Research | Peak AUC |
ST002412 | AN003931 | Metabolic effects of the protein kinase R | Macrophages | Mouse | Hudson | peak height | |
ST002926 | AN004798 | Multi-“omics” analysis reveals the orphan P. falciparum protein kinase PfPK8 regulates multi-gene family expression | Blood | Plasmodium falciparum | Malaria | Monash University | peak height |
ST003053 | AN005006 | Providing insight into the mechanism of action of Cationic Lipidated Oligomers (CLOs) using metabolomics | Bacterial cells | Staphylococcus aureus | Bacterial infection | Monash University | peak height |
ST003521 | AN005782 | Metabolic Profiling Unveils Enhanced Antibacterial Synergy of Polymyxin B and Teixobactin against Multi-Drug Resistant Acinetobacter baumannii | Bacterial cells | Acinetobacter baumannii | Bacterial infection | Monash University | peak height |
ST003521 | AN005783 | Metabolic Profiling Unveils Enhanced Antibacterial Synergy of Polymyxin B and Teixobactin against Multi-Drug Resistant Acinetobacter baumannii | Bacterial cells | Acinetobacter baumannii | Bacterial infection | Monash University | peak height |
ST000403 | AN000643 | Metabolomics-based elucidation of active metabolic pathways in erythrocytes and HSC-derived reticulocytes | Cells | Human | Monash Institute of Pharmaceutical Sciences, Monash University | Peak height | |
ST000539 | AN000819 | Metabolomics-based elucidation of active metabolic pathways in erythrocytes and HSC-derived reticulocytes (part II) | Cells | Human | Monash Institute of Pharmaceutical Sciences, Monash University | Peak height | |
ST001274 | AN002115 | Metabolomics-based profiling of the mode of action of Pathogen Box compounds in Trypanosoma brucei (part-I) | Cultured cells | Trypanosoma brucei | Sleeping sickness | Monash University | Peak height |
ST001276 | AN002117 | Development and Characterisation of a Novel Class of Aroyl Guanidine Containing Anti-Trypanosomal Compounds | Cultured cells | Trypanosoma brucei | Sleeping sickness | Monash University | Peak height |
ST003179 | AN005221 | Property and Activity Refinement of Dihydroquinazolinone-3-carboxamides as Orally Efficacious Antimalarials that Target PfATP4 | Plasmodium cells | Plasmodium falciparum | Malaria | Monash University | Peak height |
ST002815 | AN004582 | Investigation of metabolism in hypertrophic cardiomyopathy - HILIC | Heart | Mouse | Cardiomyopathy | University of California, San Francisco | peak heights |
ST002493 | AN004086 | Composition of raw plant-based food items Pilot Study | Plant | Plants | Massachusetts Institute of Technology | peak intensity | |
ST002493 | AN004090 | Composition of raw plant-based food items Pilot Study | Plant | Plants | Massachusetts Institute of Technology | peak intensity | |
ST003112 | AN005111 | Glucose Hypometabolism Prompts RAN Translation and Exacerbates C9orf72-related ALS/FTD Phenotypes | Brain | Mouse | Neurodegenerative Disorder | Thomas Jefferson University | peak intensity |
ST003113 | AN005098 | Inhibition of Asparagine Synthetase Effectively Retards Polycystic Kidney Disease Progression, investigated with targeted tracing metabolomics analysis in MEF cells using 15N2-glutamine. | Cultured cells | Mouse | Kidney disease | San Raffaele University | peak intensity |
ST003113 | AN005099 | Inhibition of Asparagine Synthetase Effectively Retards Polycystic Kidney Disease Progression, investigated with targeted tracing metabolomics analysis in MEF cells using 15N2-glutamine. | Cultured cells | Mouse | Kidney disease | San Raffaele University | peak intensity |
ST003118 | AN005112 | Glucose Hypometabolism Prompts RAN Translation and Exacerbates C9orf72-related ALS/FTD Phenotypes - Study 2 | Brain | Mouse | Neurodegenerative Disorder | Thomas Jefferson University | peak intensity |
ST001201 | AN001998 | Peroxide antimalarial treatment timecourse on trophozoite-stage P. falciparum parasites | Cultured cells | Human | Malaria | Monash University | Peak intensity |
ST001201 | AN001998 | Peroxide antimalarial treatment timecourse on trophozoite-stage P. falciparum parasites | Cultured cells | Plasmodium falciparum | Malaria | Monash University | Peak intensity |
ST001202 | AN002000 | Peroxide antimalarial treatment timecourse on ring-stage P. falciparum parasites | Cultured cells | Human | Malaria | Monash University | Peak intensity |
ST001202 | AN002000 | Peroxide antimalarial treatment timecourse on ring-stage P. falciparum parasites | Cultured cells | Plasmodium falciparum | Malaria | Monash University | Peak intensity |
ST001364 | AN002271 | Core Functional Nodes and Sex-Specific Pathways in Human Ischemic and Dilated Cardiomyopathy | Heart | Human | Cardiomyopathy | University of Sydney | Peak intensity |
ST001382 | AN002303 | Distinct metabolic states of a cell guide alternate fates of mutational buffering through altered proteostasis | Bacterial cells | E. coli | CSIR National Chemical Laboratory | Peak intensity | |
ST001547 | AN002576 | β-Adrenergic regulation of metabolism in macrophages | Macrophages | Human | Monash University | Peak intensity | |
ST001549 | AN002580 | β-Adrenergic regulation of metabolism in macrophages (part-III) | Macrophages | Human | Monash University | Peak intensity | |
ST001652 | AN002699 | Atypical Molecular Basis for Drug Resistance to Mitochondrial AQ: A Function Inhibitors in Plasmodium falciparum | Plasmodium cells | Plasmodium falciparum | Malaria | U.S. Food & Drug Administration | Peak intensity |
ST002541 | AN004186 | Methionine restriction constrains lipoylation and activates mitochondria for nitrogenic synthesis of amino acids (Part 1) | Yeast cells | Yeast | Life Sciences Institute, ZheJiang University | Peak intensity | |
ST002542 | AN004188 | Methionine restriction constrains lipoylation and activates mitochondria for nitrogenic synthesis of amino acids (Part 2) | Yeast cells | Yeast | Life Sciences Institute, ZheJiang University | Peak intensity | |
ST002542 | AN004189 | Methionine restriction constrains lipoylation and activates mitochondria for nitrogenic synthesis of amino acids (Part 2) | Yeast cells | Yeast | Life Sciences Institute, ZheJiang University | Peak intensity | |
ST002872 | AN004708 | Comparative multi-omics analyses of cardiac mitochondrial stress in three mouse models of frataxin deficiency | Heart | Mouse | Cardiomyopathy | Weill Cornell Medicine | Peak intensity |
ST002872 | AN004708 | Comparative multi-omics analyses of cardiac mitochondrial stress in three mouse models of frataxin deficiency | Heart | Mouse | Friedreichs Ataxia | Weill Cornell Medicine | Peak intensity |
ST002927 | AN004800 | O-GlcNAcase activity maintains stress granules for proximity-enhanced ATP production to ensure recovery from stress | Cultured cells | Human | Stress | Zhejiang University | Peak intensity |
ST002927 | AN004801 | O-GlcNAcase activity maintains stress granules for proximity-enhanced ATP production to ensure recovery from stress | Cultured cells | Human | Stress | Zhejiang University | Peak intensity |
ST003126 | AN005125 | Effect of high fat diet on heart metabolome of CHCHD10 mutant mice | Heart | Mouse | Cardiomyopathy | Weill Cornell Medicine | Peak Intensity |
ST003128 | AN005128 | Effect of high fat diet on serum lipidome and metabolome in CHCHD10 Mutant Mice | Blood | Mouse | Cardiomyopathy | Weill Cornell Medicine | Peak Intensity |
ST000451 | AN000707 | The alpha-1A adrenergic receptor agonist A61603 reduces cardiac polyunsaturated fatty acid-Heart raw data | Muscle | Mouse | University of North Carolina | Peak values (scaled) | |
ST001135 | AN001861 | Different dose exposure of OPC-163493 on HepG2 cells (part-I) | Hep G2 cells | Human | Diabetes | Otsuka Pharmaceuticals | pmol/1000000 cells |
ST002743 | AN004448 | Metabolomics comparison of lung fibroblasts from Pteropus alecto and Homo sapiens | Cultured cells | Black flying fox fruit bat | Duke-NUS Medical School | pmol/10^6 cells | |
ST002743 | AN004448 | Metabolomics comparison of lung fibroblasts from Pteropus alecto and Homo sapiens | Cultured cells | Human | Duke-NUS Medical School | pmol/10^6 cells | |
ST001745 | AN002840 | Metabolomic profiling of the rat hippocampus across developmental ages and after learning | Brain | Rat | New York University | pmoles/l | |
ST000337 | AN000545 | Metabolomics Approach to Allograft Assessment in Liver Transplantation | Liver | Human | Organ transplantation | Ochsner Multi-Organ Transplant Institute | pmol/mg dry powder |
ST002660 | AN004332 | MoTrPAC: Endurance exercise training study in young adult rats, Rat Gastrocnemius Powder - Targeted Acyl-CoA | Gastrocnemius | Rat | Duke University | pmol/mg of tissue | |
ST002661 | AN004333 | MoTrPAC: Endurance exercise training study in young adult rats, Rat Heart Powder - Targeted Acyl-CoA | Heart | Rat | Duke University | pmol/mg of tissue | |
ST002662 | AN004334 | MoTrPAC: Endurance exercise training study in young adult rats, Rat Liver Powder - Targeted Acyl-CoA | Liver | Rat | Duke University | pmol/mg of tissue | |
ST002663 | AN004335 | MoTrPAC: Endurance exercise training study in young adult rats, Rat White Adipose Powder - Targeted Acyl-CoA | White adipose | Rat | Duke University | pmol/mg of tissue | |
ST000174 | AN000268 | Mouse macrophages from bone marrow treatment | Macrophages | Mouse | University of Michigan | pmol/mg protein | |
ST001398 | AN002337 | Mechanism of Trichloroethylene (TCE) toxicity in the placenta | Cultured cells | Human | Environmental exposure | University of Michigan | pmol/ug |
ST000173 | AN000267 | Comparative metabolomics study of WT and iButOH tolerant E. coli | Bacterial cells | E. coli | University of Michigan | pmol/ug protein | |
ST000180 | AN000278 | 2 lines of pulmonary artery smooth muscle cells metabolic profile (122 vs 3633C central metabolic profile) | Smooth muscle | Sheep | University of Michigan | pmol/ug protein | |
ST000185 | AN000284 | Fetal Lambs vascular graft Normal v Shunt LECs | Endothelial cells | Sheep | University of Michigan | pmol/ug protein | |
ST000202 | AN000304 | THP1 Human Monocyte cells Project A (part II) | Mononuclear cells | Human | University of Michigan | pmol/ug protein | |
ST000209 | AN000311 | Glycolysis/TCA/Nucleotide_Wt_KO_TimeCourse_LPS | Macrophages | Mouse | University of Michigan | pmol/ug protein | |
ST000274 | AN000437 | HIF 1 alpha type 2 cells metabolomics | Cells | Mouse | University of Michigan | pmol/ug protein | |
ST000276 | AN000440 | IDH1 and Glioma knockdown idh1 | Glioma cells | Human | Cancer | University of Michigan | pmol/ug protein |
ST000278 | AN000443 | Viral Effect on Metabolism (part I) | Epithelial cells | Human | University of Michigan | pmol/ug protein | |
ST000278 | AN000444 | Viral Effect on Metabolism (part I) | Epithelial cells | Human | University of Michigan | pmol/ug protein | |
ST000279 | AN000445 | Viral Effect on Metabolism (part II) | Epithelial cells | Human | University of Michigan | pmol/ug protein | |
ST000295 | AN000473 | Metabolic analysis of Human and Mouse Lung Fiboblasts | Fibroblast cells | Human | University of Michigan | pmol/ug protein | |
ST000295 | AN000473 | Metabolic analysis of Human and Mouse Lung Fiboblasts | Fibroblast cells | Mouse | University of Michigan | pmol/ug protein | |
ST001759 | AN002866 | Application of the redox metabolite detection method for mouse liver | Liver | Mouse | Boston Children's Hospital, Harvard Medical School | ppm | |
ST001760 | AN002867 | Application of the redox metabolite detection method for mouse kidney | Kidney | Mouse | Boston Children's Hospital, Harvard Medical School | ppm | |
ST001762 | AN002869 | Application of the redox metabolite detection method for mouse kidney (part II) | Kidney | Mouse | Boston Children's Hospital, Harvard Medical School | ppm | |
ST001763 | AN002870 | Application of the redox metabolite detection method for mouse liver (part II) | Liver | Mouse | Boston Children's Hospital, Harvard Medical School | ppm | |
ST001764 | AN002871 | Application of the redox metabolite detection method for profiling redox state following pharmacologic perturbation with methotrexate | Cultured cells | Human | Boston Children's Hospital, Harvard Medical School | ppm | |
ST001765 | AN002872 | Optimization of redox metabolite detection in mammalian cells (part I) | Cultured cells | Human | Boston Children's Hospital, Harvard Medical School | ppm | |
ST001767 | AN002874 | Application of the redox metabolite detection method for mammalian tissues (part II) | Kidney | Mouse | Boston Children's Hospital, Harvard Medical School | ppm | |
ST001767 | AN002874 | Application of the redox metabolite detection method for mammalian tissues (part II) | Liver | Mouse | Boston Children's Hospital, Harvard Medical School | ppm | |
ST001768 | AN002875 | Application of the redox metabolite detection method for mammalian tissues (part III) | Kidney | Mouse | Boston Children's Hospital, Harvard Medical School | ppm | |
ST001768 | AN002875 | Application of the redox metabolite detection method for mammalian tissues (part III) | Liver | Mouse | Boston Children's Hospital, Harvard Medical School | ppm | |
ST001769 | AN002876 | Application of the redox metabolite detection method for profiling redox state following pharmacologic perturbations of redox balance in cells (part I) | Cultured cells | Human | Boston Childrens Hospital | ppm | |
ST001770 | AN002877 | Application of the redox metabolite detection method for profiling redox state following pharmacologic perturbations of redox balance in cells (part II) | Cultured cells | Human | Boston Children's Hospital, Harvard Medical School | ppm | |
ST001771 | AN002878 | Application of the redox metabolite detection method for profiling redox state following pharmacologic perturbations of redox balance in cells (part III) | Cultured cells | Human | Boston Children's Hospital, Harvard Medical School | ppm | |
ST001772 | AN002879 | Optimization of redox metabolite detection in mammalian cells (part II) | Cultured cells | Human | Boston Children's Hospital, Harvard Medical School | ppm | |
ST001975 | AN003223 | Anti-oxidative metabolism measurement in mammalian cells and tissues by quantitative LC/MS method (II) | Cerebrospinal fluid | Mouse | Cancer | Boston Children's Hospital, Harvard Medical School | ppm |
ST002159 | AN003535 | Chemotaxonomic patterns in intracellular metabolites of marine microbial plankton | Plankton | Marine plankton | University of Washington | presence (1), absence (0), or background level (NA) | |
ST001983 | AN003234 | Metabolomic Fingerprinting of Human High Grade Serous Ovarian Carcinoma Cell Lines | Ovarian cancer cells | Human | Cancer | University of Oklahoma Health Sciences Center | ratio |
ST003495 | AN005736 | Hepatocyte Period 1 dictates oxidative substrate selection independent of the core circadian clock | Liver | Mouse | Washington University in St. Louis | Raw Area | |
ST001752 | AN002855 | Dual RNA regulator VcdRP in V. cholerae modulates central metabolism | Bacterial cells | V. cholerae | Helmholtz Centre for Environmental Research - UFZ | relative abundance | |
ST002716 | AN004404 | Ventricle-specific myocardial protein and metabolite characterisation in healthy humans, with differential regulation in end-stage cardiomyopathies (Part 1) | Heart | Human | Cardiomyopathy | University of Sydney | Relative abundance |
ST002717 | AN004406 | Ventricle-specific myocardial protein and metabolite characterisation in healthy humans, with differential regulation in end-stage cardiomyopathies (Part 2) | Heart | Human | Cardiomyopathy | University of Sydney | Relative abundance |
ST002206 | AN003609 | Lipolysis-derived Lipids Determine Autophagy Initiation during Fasting | Worms | C. elegans | Seoul National University | relative area | |
ST000384 | AN000619 | Metabolomic profiles in P. gingivalis cells treated with pABA | Bacterial cells | Porphyromonas | Osaka University Graduate School of Dentistry | Relative Area | |
ST001668 | AN002721 | D-Allulose effects on hepatic metabolomics profile in rodents | Liver | Rat | Matsutani Chemical Industry Co., Ltd. | Relative Area | |
ST002719 | AN004408 | Comparison of metabolic of A549 cells before and after Gossypol acetate (GAA) treatment | Lung | Human | Cancer | Hangzhou Institute of Medicine (HIM), University of Chinese Academy of Sciences (Zhejiang Cancer Hospital), Chinese Academy of Sciences | relative intensity |
ST001869 | AN003031 | WNK463 Inhibition on Right Ventricular metabolomics | Heart | Rat | Hypertension | University of Minnesota | relative value |
ST001870 | AN003032 | Effects of GP130 Antagonism on Right Ventricular Metabolism in Monocrotaline Rats | Heart | Rat | University of Minnesota | relative value | |
ST001304 | AN002173 | Multi-omics analysis delineates the distinct functions of sub-cellular acetyl-CoA pools in Toxoplasma gondii | Fibroblast cells | Toxoplasma gondii | Parasitic infection | Monash University | Signal Intensity |
ST001198 | AN001994 | Targeted LC-MS/MS Analysis of Soluble Metabolites in the MeOH:H2O Phase (part-IV) | Bacterial cells | Synechococcus | Colorado State University | spectral abundance per cell | |
ST000176 | AN000271 | cell and liver metabolomics | Liver | Mouse | Florida State University | SUC | |
ST000815 | AN001292 | db/db WT ozone and air exposed mice | Lung | Mouse | Ozone Stress | Harvard School of Public Health | total ion counts |
ST000143 | AN000226 | Metabolic analysis of Normal Mouse Lung Fiboblasts with/without TGFbeta treatment (Part 1) | Fibroblast cells | Mouse | University of Michigan | uM | |
ST000171 | AN000265 | cell metabolomics (metabolic phenotypes of a clock mutant mouse) | Fibroblast cells | Mouse | Florida State University | uM | |
ST000183 | AN000281 | Metabolic analysis of Parp1 ko/wt Saline & Bleo Mouse Lung Fiboblasts and Human IPF & Normal Lung Fiboblasts (Part 3) | Fibroblast cells | Mouse | University of Michigan | uM | |
ST000313 | AN000499 | Muscle Clock knock out mice metabolic changes (iMSBmal1-Exp1) | Muscle | Mouse | University of Michigan | uM | |
ST000828 | AN001836 | Metabolic analysis of Parp1 ko/wt Saline & Bleo Mouse Lung Fiboblasts and Human IPF & Normal Lung Fiboblasts 3 | Cultured cells | Human | Lung disease | University of Michigan | uM |
ST003297 | AN005401 | Metabolomic profiling of cultured TRAMP-C2 cells in the presence or absence of PD-L1. | Cultured cells | Mouse | Cancer | University of Ottawa | uM |
ST000312 | AN000498 | IDH1R132H activity in glioma cell lines and tumnor tissue (2HG) | Cells | Mouse | Cancer | University of Michigan | uM/500ul extraction solvent |
ST000275 | AN000438 | Metabolic analysis of Parp1 ko/wt Saline & Bleo Mouse Lung Fiboblasts and Human IPF & Normal Lung Fiboblasts (Part 2) | Fibroblast cells | Mouse | University of Michigan | uM (500ul of extraction solvent) | |
ST000176 | AN000270 | cell and liver metabolomics | Liver | Mouse | Florida State University | uM (in 500 ul extract) | |
ST002212 | AN003617 | Human fecal metabolome profiles under 3 different dietary terms | Feces | Human | Keio University | µmol/g | |
ST003267 | AN005353 | FDX2-KO induces global down-regulation of iron-sulfur cluster-containing proteins and senescence-like growth arrest or death in ovarian cancer cells | Cultured cells | Human | Cancer | Tohoku University | μmol/g-protein |