List of Studies ( Metabolite:Sedoheptulose 7-phosphate)
Study_id | Analysis_id | Study_title | Source | Species | Disease | Institute | Units(range) |
---|---|---|---|---|---|---|---|
ST001680 | AN002739 | 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 |
ST001447 | AN002418 | Metabolomics of lung injury after allogeneic hematopoietic cell transplantation - Colon ICMS | Intestine | Mouse | Graft versus host disease | University of Kentucky | abundance & normalized peak area |
ST001453 | AN002428 | Metabolomics of lung injury after allogeneic hematopoietic cell transplantation - Liver ICMS | Liver | Human | Graft versus host disease | University of Kentucky | abundance & normalized peak area |
ST001470 | AN002446 | Metabolomics of lung injury after allogeneic hematopoietic cell transplantation - Lung ICMS | Mouse | Graft versus host disease | University of Kentucky | abundance & normalized peak area | |
ST001472 | AN002448 | Metabolomics of lung injury after allogeneic hematopoietic cell transplantation - Small Intestines ICMS | SI | Mouse | Graft versus host disease | University of Kentucky | abundance & normalized peak area |
ST001986 | AN003237 | Fbxo7 promotes Cdk6 activity to inhibit PFKP and glycolysis in T cells | T-cells | Mouse | University of Cambridge | arbitrary unit | |
ST000509 | AN000781 | Metabolic changes to maternal rat liver tissue during and post-pregnancy | Liver | Rat | University of Colorado, Denver | Arbitrary units | |
ST000510 | AN000783 | Assessing metabolic changes to maternal rat liver tissue during and post-pregnancy (part II) | Liver | Mouse | University of Colorado, Denver | 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 |
ST003254 | AN005336 | The impact of grass- and grain-finishing on metabolomic profiles of North American Black Angus Beef cattle. | Bovine meat | Cow | Duke University | Arbitrary Units | |
ST002316 | AN003783 | Differential requirements for mitochondrial electron transport chain components in the adult murine liver - Untargeted Metabolomics (qTOF) | Liver | Mouse | Metabolic syndrome | The University of Texas Southwestern Medical Center at Dallas | area |
ST002369 | AN003864 | The impact of acute Colony Stimulating Factor 1 treatment on serum and liver metabolites in fed and fasted mice LIVER | Liver | Mouse | The University of Queensland | area | |
ST000172 | AN000266 | THP1 Human Monocyte cells Project A (part I) | Mononuclear cells | Human | University of Michigan | Area normalized to protein | |
ST002702 | AN004379 | A targeted metabolomics approach for sepsis-induced ARDS and its subphenotypes | Blood | Human | Acute respiratory distress syndrome | Asan Medical Center | area ratio |
ST002245 | AN003665 | Deciphering the metabolomic differences between two fast-growing cyanobacteria, S.elongatus PCC 11801 and 11802 via metabolite profiling | Bacterial cells | Synechococcus elongatus | Indian Institute of Technology Bombay | Area Ratios | |
ST000450 | AN000706 | Metabolic features of chronic fatigue syndrome | Blood | Human | Myalgic encephalomyelitis/chronic fatigue syndrome | University of California, San Diego | Area under curve |
ST000465 | AN000726 | Uniquely Tumor-Selective Englerin A Profoundly Alters Lipid Metabolism in Renal Cell Carcinoma inducing ER-Stress and an Acute Inflammatory Response | Kidney | Human | Cancer | University of California, San Diego | Area under curve |
ST001143 | AN001883 | Microbial depletion and ozone exposure - Lung tissue (part I) | Lung | Mouse | Asthma | Harvard School of Public Health | Area under curve |
ST001401 | AN002343 | Steady-state metabolomics time course of Saccharomyces cerevisiae mitochondrial fatty acid synthesis (mtFAS) mutants | Yeast cells | Yeast | University of Utah | Area under curve | |
ST001901 | AN003089 | Mitochondrial-Derived Compartments Facilitate Cellular Adaptation to Amino Acid Stress | Yeast cells | Yeast | University of Utah School of Medicine | area under the curve | |
ST001901 | AN003090 | Mitochondrial-Derived Compartments Facilitate Cellular Adaptation to Amino Acid Stress | Yeast cells | Yeast | University of Utah School of Medicine | area under the curve | |
ST001901 | AN003092 | Mitochondrial-Derived Compartments Facilitate Cellular Adaptation to Amino Acid Stress | Yeast cells | Yeast | University of Utah School of Medicine | area under the curve | |
ST002840 | AN004647 | Collaborative role of YqgC and superoxide dismutase (MnSOD) in manganese intoxication: Replicate Experiment 1 | Bacterial cells | Bacillus subtilis | Cornell University | Area under the curve | |
ST002841 | AN004649 | Collaborative role of YqgC and superoxide dismutase (MnSOD) in manganese intoxication: Replicate Experiment 2 | Bacterial cells | Bacillus subtilis | Cornell University | Area under the curve | |
ST003519 | AN005777 | Effect of insluin on metabolism of ex vivo ischemia heart | Heart | Brown Rat | Heart disease | Mayo Clinic | Area under the Curve |
ST001908 | AN003105 | Post Acute Myocardial Infarction Left Ventricular Remodeling Bio marker Analysis (PAMILA) | Blood | Human | Heart disease | National University of Singapore | a.u. |
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. |
ST003082 | AN005040 | Metabolome changes in embryonic CSF (Part 4) | CSF | Mouse | Autism | Boston Children's Hospital, Harvard Medical School | a.u. |
ST003083 | AN005041 | Metabolome changes in embryonic CSF (Part 5) | CSF | 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. |
ST001260 | AN002091 | Metabolic changes of Fusobacterium nucleatum when co-cultured with other oral microbes (part-I) | Bacterial cells | Fusobacterium nucleatum | Osaka University Graduate School of Dentistry | AU | |
ST001261 | AN002093 | Metabolic changes of culture supernatants of Fusobacterium nucleatum co-cultured with other oral microbes (part-II) | Bacterial cells | Fusobacterium nucleatum | Osaka University Graduate School of Dentistry | AU | |
ST002058 | AN003351 | Muscle/Lung/Tumor metabolomics | Lung | Mouse | Cancer | University of Colorado Anschutz Medical Campus | AU |
ST002058 | AN003351 | Muscle/Lung/Tumor metabolomics | Muscle | Mouse | Cancer | University of Colorado Anschutz Medical Campus | AU |
ST002059 | AN003353 | 4T1 and SkM cells | Cultured cells | Human | Cancer | University of Colorado Anschutz Medical Campus | AU |
ST002123 | AN003476 | GCN2 regulates mitochondrial OXPHOS in HSPCs under proliferation conditions. | Bone marrow | Mouse | Sun Yat-sen University | AU | |
ST002204 | AN003607 | Endothelial Sirtuin1 Suppresses Whole-body Insulin Sensitivity by Modulating the Secretome | Muscle | Mouse | Diabetes | University of Iowa | AU |
ST003546 | AN005825 | Improved Soil Health and Pasture Phytochemical Richness Underlies Improved Beef Nutrient Density in Southern US Grass-Finished Beef Systems | Muscle | Cattle | Utah State University | AU | |
ST003546 | AN005827 | Improved Soil Health and Pasture Phytochemical Richness Underlies Improved Beef Nutrient Density in Southern US Grass-Finished Beef Systems | Muscle | Cattle | Utah State University | 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 | |
ST001074 | AN001756 | Open source discovery of starting points for next generation chemoprotective antimalarial drugs (Biofocus 1) | Parasite | Human | Pennsylvania State University | Average Peak Area | |
ST001878 | AN003081 | Targeted analysis of Babesia divergens merozoites | Merozoites | Blood parasite | Universidad CEU San Pablo | blank-substracted abundances | |
ST002457 | AN004009 | Mouse kidney metabolomics (Whole kidney) | Kidney | Mouse | Chronic kidney disease | Hadassah Medical Center | concentration |
ST002925 | AN004797 | Metabolite analysis of hepatic Pptc7-ko mice under fed or fasting conditions | Liver | Mouse | National Institute of Biological Sciences, Beijing | count | |
ST002178 | AN003567 | Age-independent Cardiac Protection by Pharmacological Activation of Beclin-1 During Endotoxemia and Its Association with Energy Metabolic Reprograming in Myocardium — A Targeted Metabolomics Study | Heart | Mouse | Endotoxemia | Loyola University Chicago Stritch School of Medicine | count per second (cps) |
ST003060 | AN005015 | Fluxomics of hormone deprivation in ER+ breast cancer cell lines | Breast cancer cells | Human | Cancer | Dartmouth College | counts |
ST000718 | AN001123 | Targeted Metabolomics in Pediatric US Population Exposed to Low-Level Heavy Metals | Cultured cells | Human | Environmental exposure | University of Michigan | Counts |
ST001402 | AN002344 | Ontogeny related changes in the pediatric liver metabolome | Liver | Human | Moffitt Cancer Center | estimated abundances | |
ST001403 | AN002345 | Ontogeny related changes in the pediatric liver metabolome (part-II) | Liver | Human | Moffitt Cancer Center | estimated abundances | |
ST001178 | AN001955 | Metabolomic analysis of C2C12 myoblasts induced by the transcriptional factor FOXO1 | Muscle | Mouse | Kyoto Prefectural University | fold | |
ST002555 | AN004207 | Ethnicity-Specific Differences in Ovarian Cancer Metabolic Signatures | Cultured cells | Human | Cancer | University of Oklahoma Health Sciences Center | Fold change over standard |
ST002379 | AN003878 | Glucose flux analysis of NLRP3 inflammasome activated macrophages | Macrophages | Mouse | Wake Forest School of Medicine | Fractional enrichment | |
ST002797 | AN004550 | Fetal metabolic adaptations to cardiovascular stress in twin-twin transfusion syndrome | Amniotic fluid | Human | Twin-twin transfusion syndrome | University of Texas Health Science Center at Houston | intensity |
ST002069 | AN003379 | Systemic impact of the expression of the mitochondrial alternative oxidase on Drosophila development | Larvae | Fruit fly | Tampere University | intensity (area under the curve) | |
ST002119 | AN003468 | Metabolomics analysis of zebrafish response to CID661578 treatment | Larvae | Zebrafish | Diabetes | North Carolina State University | ion counts |
ST002152 | AN003524 | Metabolomics analysis of mouse liver with or without SIRT5 deficiency | Liver | Mouse | North Carolina State University | ion counts | |
ST003454 | AN005675 | Branched chain alpha-ketoacids impact pulmonary artery smooth muscle cell metabolism | Cultured cells | Human | Hypertension | Peking University | ion intensity |
ST003455 | AN005676 | Metabolic alterations in pulmonary artery smooth muscle cells of idiopathic pulmonary arterial hypertension (IPAH) patients. | Cultured cells | Human | Hypertension | Peking University | ion intensity |
ST003501 | AN005749 | TREM2 expression level is critical for microglial state, metabolic capacity and efficacy of TREM2 agonism | Microglia | Mouse | Alzheimers disease | Denali Therapeutics | log2(area) |
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 | AN005589 | 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 | |
ST001320 | AN002196 | Examination of labeled glucose utilization in central carbon metabolism in HeLa cells post WNT stimulation | Cultured cells | Human | Cancer | University of California, Los Angeles | MS1 AUC integration |
ST002477 | AN004046 | Neutrophil metabolomics in COVID-19 | Neutrophils | Human | COVID-19 | UT Southwestern Medical Center | MS reading |
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 |
ST000712 | AN001112 | Diabetic heart adrenergic signaling and metabolism (STZ & Isoproterenol, High Fat) | Muscle | Mouse | Diabetes | University of Michigan | nmol/mg |
ST000752 | AN001180 | Effect of cooling on muscle tissue metabolism | Muscle | Human | University of Michigan | nmol/mg | |
ST000755 | AN001329 | Rat Retinal Detachment Metabolomics Timecourse (part II) | Eye tissue | Rat | University of Michigan | nmol/mg | |
ST000834 | AN001425 | Purine and TCA measurements in salt sensitive (SS) hypertension | Kidney | Rat | Hypertension | University of Michigan | nmol/mg |
ST000839 | AN001345 | Effect of cooling on muscle tissue metabolism (part II) | Muscle | Human | University of Michigan | nmol/mg | |
ST000840 | AN001844 | Diabetic heart adrenergic signaling and metabolism (STZ & Isoproterenol, High Fat) - part II | Heart | Mouse | Diabetes | University of Michigan | nmol/mg |
ST003143 | AN005157 | Mitochondrial complex I promotes kidney cancer metastasis | Kidney | Human | Cancer | University of Texas Southwestern Medical Center at Dallas | Normalized Abundance |
ST003143 | AN005157 | Mitochondrial complex I promotes kidney cancer metastasis | Tumor cells | Human | Cancer | University of Texas Southwestern Medical Center at Dallas | Normalized Abundance |
ST003143 | AN005158 | Mitochondrial complex I promotes kidney cancer metastasis | Kidney | Human | Cancer | University of Texas Southwestern Medical Center at Dallas | Normalized Abundance |
ST003143 | AN005158 | Mitochondrial complex I promotes kidney cancer metastasis | Tumor cells | Human | Cancer | University of Texas Southwestern Medical Center at Dallas | Normalized Abundance |
ST002285 | AN003737 | Multiplatform mass spectrometry-based analysis of Leishmania donovani infected macrophages at different time points after infection | Cultured cells | Human | Parasitic infection | Universidad CEU San Pablo | Normalized abundances |
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 |
ST002322 | AN003789 | Metabolomics study comparing SCAP KO and WT B cells | Cultured cells | Mouse | Indiana University School of Medicine | Normalized AUC | |
ST003193 | AN005241 | Metabolomics study on frozen tissue derived from the tumor and adjacent non-malignant liver tissue (NML) of patient afflicted with fibrolamellar carinoma (FLC) | Liver | Human | Cancer | Cornell University | normalized-BatchCorrected-Imputed-log2transformed Intensity |
ST003193 | AN005241 | Metabolomics study on frozen tissue derived from the tumor and adjacent non-malignant liver tissue (NML) of patient afflicted with fibrolamellar carinoma (FLC) | Lung | Human | Cancer | Cornell University | normalized-BatchCorrected-Imputed-log2transformed Intensity |
ST003193 | AN005241 | Metabolomics study on frozen tissue derived from the tumor and adjacent non-malignant liver tissue (NML) of patient afflicted with fibrolamellar carinoma (FLC) | Lymph node | Human | Cancer | Cornell University | normalized-BatchCorrected-Imputed-log2transformed Intensity |
ST003193 | AN005241 | Metabolomics study on frozen tissue derived from the tumor and adjacent non-malignant liver tissue (NML) of patient afflicted with fibrolamellar carinoma (FLC) | Peritoneal fluid | Human | Cancer | Cornell University | normalized-BatchCorrected-Imputed-log2transformed Intensity |
ST003193 | AN005241 | Metabolomics study on frozen tissue derived from the tumor and adjacent non-malignant liver tissue (NML) of patient afflicted with fibrolamellar carinoma (FLC) | Spinal cord | Human | Cancer | Cornell University | normalized-BatchCorrected-Imputed-log2transformed Intensity |
ST000367 | AN000600 | Distinctly perturbed metabolic networks underlie differential tumor tissue damages induced by immune modulator b-glucan in a two-case ex vivo non-small cell lung cancer study | Lung | Human | Cancer | University of Kentucky | normalized corrected peak area |
ST000367 | AN000601 | Distinctly perturbed metabolic networks underlie differential tumor tissue damages induced by immune modulator b-glucan in a two-case ex vivo non-small cell lung cancer study | Lung | Human | Cancer | University of Kentucky | normalized corrected peak area |
ST002009 | AN003275 | Metabolomics analysis of stress erythroid progenitors | Stem cells | Mouse | Inflammation | Pennsylvania State University | Normalized peak area |
ST002825 | AN004609 | Brain Metabolomics in Fragile X-Associated Tremor/Ataxia Syndrome (FXTAS) | Brain | Human | Neurodegenerative disease | UC Davis | normalized peak heights |
ST002330 | AN003802 | Early-stage responses to Plasmodiophora brassicae at the metabolome levels in clubroot resistant and susceptible oilseed Brassica napus | Plant | Canola | Clubroot disease | Trent University | normalized relative level |
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) |
ST001747 | AN002843 | Lung metabolomics after ischemic acute kidney injury reveals increased oxidative stress, altered energy production, and ATP depletion | Lung | Mouse | Acute kidney injury | University of Colorado Anschutz Medical Campus | peak area |
ST002007 | AN003270 | Isotope tracing analysis of stress erythroid progenitors | Cultured cells | Mouse | Inflammation | Pennsylvania State University | peak area |
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 |
ST002011 | AN003279 | 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 |
ST002153 | AN003526 | Data from plasma metabolome analysis of APP-KI and Wild type mice treated with B. breve MCC1274 | Blood | Mouse | Morinaga milk industry CO., LTD. | peak area | |
ST002163 | AN003544 | Remote solid cancers rewire hepatic nitrogen metabolism via host nicotinamide-N-methyltransferase | Liver | Mouse | Cancer | Tohoku 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 |
ST002220 | AN003629 | Cataboslim of branched-chain amino acids (BCAAs) in renal cells HK2 and 786-O | Cultured cells | Human | 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 |
ST002225 | AN003634 | Time sensitive contribution of the BCAA catabolism to the TCA cycle carbons in HK2, 786-O, OS-RC-2 and RFX-631 | 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 | |
ST002371 | AN003866 | High-resolution metabolomics analysis of NLRP3 inflammasome activated macrophages | Macrophages | Mouse | Inflammation | Wake Forest School of Medicine | peak area |
ST002431 | AN003957 | MS profiling of the Long Term Evolution Experiment | Bacterial cells | E. coli | Rutgers University | 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 |
ST003162 | AN005187 | Loss of dihydroceramide desaturase drives neurodegeneration by disrupting endoplasmic reticulum and lipid droplet homeostasis in glial cells | CNS | Drosophila melanogaster | Brain disease | Washington University in St. Louis | peak area |
ST003162 | AN005187 | Loss of dihydroceramide desaturase drives neurodegeneration by disrupting endoplasmic reticulum and lipid droplet homeostasis in glial cells | Larvae | Drosophila melanogaster | Brain disease | Washington University in St. Louis | peak area |
ST003162 | AN005188 | Loss of dihydroceramide desaturase drives neurodegeneration by disrupting endoplasmic reticulum and lipid droplet homeostasis in glial cells | CNS | Drosophila melanogaster | Brain disease | Washington University in St. Louis | peak area |
ST003162 | AN005188 | Loss of dihydroceramide desaturase drives neurodegeneration by disrupting endoplasmic reticulum and lipid droplet homeostasis in glial cells | Larvae | Drosophila melanogaster | Brain disease | Washington University in St. Louis | peak area |
ST003347 | AN005482 | ADSL deficiency drives mitochondrial dysfunction and ERK2 dysregulation in a linear genotype to phenotype correlation | Skin | Human | Neuropathy | Catholic University of the Sacred Heart | 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 | |
ST000164 | AN000257 | Metabolomic analysis of normal and diabetic mouse bone marrow under PBS or metformin treatment | Bone marrow | Mouse | Diabetes | New York University | 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 |
ST000231 | AN000345 | Comprehensive analysis of transcriptome and metabolome in Intrahepatic Cholangiocarcinoma and Hepatocellular Carcinoma (part II) | Liver | Human | Cancer | Osaka City University | 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 | |
ST001158 | AN001916 | The gut microbiota plays a central role to modulate the plasma metabolome in response to chronic Angiotensin II infusion (part-II) | Feces | Mouse | Johns Hopkins University School of Medicine | Peak area | |
ST001218 | AN002031 | Wild type versus TRACK Mice on regular chow and Vitamin A deprived diet | Kidney | Mouse | Cancer | weill cornell medicine | 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 |
ST001329 | AN002215 | SS-31 and NMN: Two Paths to Improve Metabolism and Function in Aged Hearts | Heart | Mouse | University of Washington | 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 | AN002408 | 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 | |
ST001611 | AN002646 | 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 | AN002646 | 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 | |
ST002492 | AN004081 | Composition of raw plant-based food items | Plant | Plants | Northeastern University | Peak area | |
ST003249 | AN005322 | Mitochondrial respiration impairment in microglia dampens response to demyelinating injury but is not sufficient to induce an aging phenotype | Microglia | Mouse | Alzheimers disease | Northwestern University | Peak area |
ST003262 | AN005346 | A Covalent Creatine Kinase Inhibitor Ablates Glioblastoma Migration and Sensitizes Tumors to Oxidative Stress. | Brain | Human | Cancer | Northwestern University, Feinberg School of Medicine | 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 |
ST002754 | AN004470 | Metabolomics analysis of maternal obesity model | Blood | Mouse | Fatty liver disease | University of Bonn | 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 |
ST002984 | AN004903 | Amino acid catabolite markers for early prognostication of pneumonia in patients with COVID-19 | Blood | Human | COVID-19 | Graduate School of Medicine, Kyoto University | Peak area/Internal Standard |
ST000308 | AN000488 | 13C mass isotopomer analysis (LCMS flux studies) MLL-AF9 (part I) | Cells | Mouse | University of Michigan | Peak area normalized | |
ST002499 | AN004106 | Metabolomics analysis of stress erythroid progenitors (Part 2) | Stem cells | Mouse | Inflammation | Pennsylvania State University | peak area normalized to IS and cell number |
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 | |
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 |
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 |
ST000352 | AN000574 | Metabolic profiling reveals biochemical pathways and potential biomarkers associated with the pathogenesis of Krabbe disease | Brain | Mouse | Krabbe disease | University at Buffalo | 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 |
ST003160 | AN005185 | New class of heterospirocyclic compounds present strong and rapid activity against artemisinin- and multidrug-resistant P. falciparum parasites | Plasmodium cells | Plasmodium falciparum | Malaria | Monash University | Peak height |
ST003179 | AN005222 | Property and Activity Refinement of Dihydroquinazolinone-3-carboxamides as Orally Efficacious Antimalarials that Target PfATP4 | Plasmodium cells | Plasmodium falciparum | Malaria | Monash University | Peak height |
ST002952 | AN004849 | Investigate the impact of feeding time on the hexosamine biosynthetic pathway (HBP) in the mouse liver and heart using targeted metabolomics: primary metabolism | Heart | Mouse | University of California, Davis | peak heights | |
ST002952 | AN004849 | Investigate the impact of feeding time on the hexosamine biosynthetic pathway (HBP) in the mouse liver and heart using targeted metabolomics: primary metabolism | Liver | Mouse | University of California, Davis | peak heights | |
ST002284 | AN003733 | Genetically defined human GBM organoids reveal principles of GBM development and actionable targets | Cultured cells | Human | Cancer | DKFZ | peak intensity |
ST000614 | AN000940 | Tobacco-specific carcinogens in Bladder Cancer | Bladder | Human | Cancer | Baylor College of Medicine | Peak intensity |
ST001309 | AN002179 | Metabolite expression in liver after early life exposure to an endocrine disruptor at 240 days postnatal (part-I) | Liver | Rat | Environmental exposure | Baylor College of Medicine | 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 | |
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 |
ST002270 | AN003711 | Xenopus tropicalis glycolysis and PPP inhibition | Tail | Western clawed frog | University of Washington | 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) | |
ST003313 | AN005425 | Integrative analysis of serum and fecal metabolome and the microbiome that herald Crohn Disease flare - feces | Feces | Human | Inflammatory bowel disease; Crohn disease | Sheba hospital | percentage of metabolites per sample |
ST002989 | AN004909 | Targeting NPM1 Epigenetically Promotes Post-infarction Cardiac Repair by Reprogramming Reparative Macrophage Metabolism | Bone marrow | Mouse | Cardiovascular disease | Renji Hospital, Shanghai Jiao Tong University School of Medicine | pmol |
ST001135 | AN001861 | Different dose exposure of OPC-163493 on HepG2 cells (part-I) | Hep G2 cells | Human | Diabetes | Otsuka Pharmaceuticals | pmol/1000000 cells |
ST002061 | AN003360 | Glutamine flux in macrophages treated with stable-isotope labeled analog 4 mM (U-13C5) glutamine | Macrophages | Mouse | Shanghai Jiao Tong University affiliated Renji Hospital | pmoles/I | |
ST001745 | AN002840 | Metabolomic profiling of the rat hippocampus across developmental ages and after learning | Brain | Rat | New York University | pmoles/l | |
ST000838 | AN001343 | Obesity and marrow and marrow adipose tissue (MAT) metabolomics | Adipose tissue | Mouse | Obesity | University of Michigan | pmol/mg |
ST000838 | AN001343 | Obesity and marrow and marrow adipose tissue (MAT) metabolomics | Bone marrow | Mouse | Obesity | University of Michigan | pmol/mg |
ST000740 | AN001154 | Quantitating the baseline fatty acid composition in phospholipids in subgroups of tumor cells | Tumor cells | Human | Cancer | University of Michigan | pmol/mg protein |
ST000767 | AN001213 | Metabolite analysis of regional neural stem/progenitor cells | Stem cells | Mouse | University of Michigan | pmol/mg protein | |
ST000375 | AN000609 | Mice exercise metabolomics (part II) | Blood | Mouse | University of Michigan | pmol/mg tissue | |
ST001398 | AN002337 | Mechanism of Trichloroethylene (TCE) toxicity in the placenta | Cultured cells | Human | Environmental exposure | University of Michigan | pmol/ug |
ST000178 | AN000274 | T cell metabolism during graft-versus-host disease (CAB 307)-PART I | T-cells | Mouse | 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 | |
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 | |
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 | |
ST000373 | AN000607 | Measure change in metabolites based on diet and feeding status (part II) | Brain | Fruit fly | University of Michigan | pmol/ug protein | |
ST000835 | AN001337 | Deubiquitinase inhibitor compound C6 effect on cellular metabolism | Cultured cells | Mouse | University of Michigan | pmol/ug protein | |
ST000837 | AN001340 | Hepatocyte Differentiation Metabolism | Stem cells | Human | University of Michigan | pmol/ug protein | |
ST001008 | AN001650 | Multi-Platform Physiologic and Metabolic Phenotyping Reveals Microbial Toxicity (part II) | Intestine | Mouse | Pennsylvania State University | ppm | |
ST001299 | AN002163 | Metatranscriptomic Analysis of the Mouse Gut Microbiome Response to the Persistent Organic Pollutant 2,3,7,8-Tetrachlorodibenzofuran | Intestine | Mouse | The Pennsylvania State University (Penn State) | ppm | |
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 | |
ST001766 | AN002873 | Application of the redox metabolite detection method for mammalian tissues (part I) | Kidney | Mouse | Boston Children's Hospital, Harvard Medical School | ppm | |
ST001766 | AN002873 | Application of the redox metabolite detection method for mammalian tissues (part I) | Liver | Mouse | 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 | |
ST001773 | AN002880 | Application of the redox metabolite detection method for mouse biofluids (part II) | Blood | Mouse | 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 |
ST001977 | AN003225 | Anti-oxidative metabolism measurement in mammalian cells and tissues by quantitative LC/MS method (IV) | Cerebrospinal fluid | Human | Cancer | Boston Children's Hospital, Harvard Medical School | ppm |
ST001978 | AN003226 | Anti-oxidation metabolism measurement in mammalian cells and tissues by quantitative LC/MS method (V) | Cerebrospinal fluid | Human | Cancer | Boston Children's Hospital, Harvard Medical School | ppm |
ST003080 | AN005038 | Metabolome changes in embryonic CSF (Part 2) | CSF | Mouse | Autism | Boston Children's Hospital, Harvard Medical School | ppm |
ST002805 | AN004561 | IL-1β-mediated adaptive re-programming of endogenous human cardiac fibroblasts to cells with immune features during fibrotic remodeling | Cultured cells | Human | Pulmonary hypertension | Brown University | Q3 Peak Area (area under curve) |
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 | |
ST001835 | AN002977 | Use of Integrated Metabolomics, Transcriptomics, and Signal Protein Profile to Characterize the Effector Function and Associated Metabotype of Polarized Macrophage Phenotypes | Blood | Human | Idaho Veterans Research and Education Foundation | raw area count | |
ST003035 | AN004976 | Central Transcriptional Regulator Controls Growth and Carbon Storage under High Light Stress in Photosynthetic Microalgae Model Strains | Algae | Picochlorum celeri | National Renewable Energy Lab | Raw Area Count | |
ST003131 | AN005135 | Untargeted Metabolomics on mouse caecal contents | Cecum | Mouse | University College Cork | Raw Peak Area | |
ST003132 | AN005141 | Untargeted Metabolomics on Mouse colonic mucosa | Colonic mucosa | Mouse | University College Cork | Raw Peak Area | |
ST003211 | AN005266 | Fetal growth delay caused by loss of non-canonical imprinting is resolved late in pregnancy and culminates in offspring overgrowth | Blood | Mouse | Hudson Institute of Medical Research | Relative abundance | |
ST001404 | AN002346 | Ontogeny related changes in the pediatric liver metabolome (part-III) | Liver | Human | Moffitt Cancer Center | Relative Abundance | |
ST001644 | AN002689 | In Vitro Characterization and Metabolomic Analysis of Cold-Stored Platelets | Blood | Human | University of Colorado Anschutz Medical Campus | Relative Abundance | |
ST002837 | AN004639 | Bacterial tryptophan metabolites increased by prebiotic galactooligosaccharide reduce microglial reactivity and are associated with lower anxiety-like behavior (Blood) | Blood | Mouse | Anxiety | National Center for Advancing Translational Sciences | Relative Abundance |
ST002206 | AN003609 | Lipolysis-derived Lipids Determine Autophagy Initiation during Fasting | Worms | C. elegans | Seoul National University | relative area | |
ST002584 | AN004255 | Metabolomics analysis of ALDH1L1-expressing HuH7 cell lines. | Cultured cells | Human | Cancer | Tohoku Medical and Pharmaceutical University | relative area |
ST001439 | AN002403 | Metabolites in contents of small intestine in wild type and DAOG181R/G181R mice | Intestine | Mouse | KEIO University School of Medicine | 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 | |
ST003483 | AN005720 | Tissue niche influences immune and metabolic profiles to Staphylococcus aureus biofilm infection (Extracellular data) | Brain, Galea, PJI Tissue | Mouse | Bacterial infection | UNMC | Relative intensities |
ST002106 | AN003445 | Genetic and chemical validation of Plasmodium falciparum aminopeptidase PfA-M17 as a drug target in the hemoglobin digestion pathway (Part 1) | Blood | Plasmodium falciparum | Malaria | Monash University | relative intensity |
ST002107 | AN003447 | Genetic and chemical validation of Plasmodium falciparum aminopeptidase PfA-M17 as a drug target in the hemoglobin digestion pathway (Part 2) | Blood | Plasmodium falciparum | Malaria | Monash University | relative intensity |
ST002108 | AN003448 | Genetic and chemical validation of Plasmodium falciparum aminopeptidase PfA-M17 as a drug target in the hemoglobin digestion pathway (Part 3) | Blood | Plasmodium falciparum | Malaria | Monash University | relative intensity |
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 |
ST001167 | AN001930 | Comprehensive Profiling by Non-targeted Stable Isotope Tracing Capillary Electrophoresis-Mass Spectrometry | Cultured cells | Human | Cancer | Dalian Institute Of Chemical Physics, Chinese Academy Of Sciences | Relative intensity after normalization |
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 | |
ST002018 | AN003288 | Multi-omic analysis of the microbiome and metabolome in healthy subjects (feces) | Feces | Human | Vanderbilt University Medical Center | scaled imputed | |
ST002231 | AN003641 | Metabolomics Analysis of HOG-EV and HOG-R132H Cells with and without BAY 2402234 Treatment | Cultured cells | Human | Cancer | UT Southwestern Medical Center | TIC-Corrected Peak Area |
ST000815 | AN001290 | db/db WT ozone and air exposed mice | Lung | Mouse | Ozone Stress | Harvard School of Public Health | total ion counts |
ST003161 | AN005186 | Diet-omics in the Study of Urban and Rural Crohn disease Evolution (SOURCE) cohort | Feces | Human | Inflammatory bowel disease | Sheba hospital | TSS normalized values |
ST000841 | AN001355 | Metabolomics of muscle in insulin sensitive and resistant obese indivduals. | Muscle | Human | Obesity | University of Michigan | ug/100 mg |
ST000842 | AN001363 | Muscle and plasma before and after exercise | Blood | Human | Obesity | University of Michigan | ug/100 mg |
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 |
ST000833 | AN001841 | Influence of murine norovirus on cell metabolism | Cultured cells | Mouse | University of Michigan | uM | |
ST002171 | AN003558 | Serum metabolome of specific-pathogen-free mice fed with five distinct rodent diets with varying fiber content and source. | Blood | Mouse | Luxembourg Institute of Health | 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 |
ST000182 | AN000280 | Bone Marrow Metabolomics (part I) | Bone marrow | Mouse | University of Michigan | uM (100ug/ml protein per sample) | |
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) | |
ST000769 | AN001216 | Metabolomics of Lin-Sca1+Kit+ (LSK) cells in NM mice | Bone marrow | Mouse | University of Michigan | uM/ng protein | |
ST000824 | AN001310 | 2HG concentration in human IDH1m cells | Glioma cells | Human | Cancer | University of Michigan | uM/ng protein |
ST002397 | AN003904 | System-level analysis of flux regulation of yeast show that glycolytic flux is controlled by allosteric regulation and enzyme phosphorylation | Cells | Yeast | Shanghai Center for Systems Biomedicine, Shanghai Jiaotong University | umol/l | |
ST001253 | AN002081 | Phenotyping Mouse blood metabolites in day and night in type 2 diabetes | Blood | Mouse | Diabetes | Indiana University School of Medicine | VolNormImp Area counts |
ST002201 | AN003604 | Multi-omics profiling of 5 Arabidopsis accessions in response to combined water and nitrogen deficiencies. | Plant | Arabidopsis thaliana | Stress | INRAE | µg/mg FW and arbitrary/mg FW |
ST002212 | AN003617 | Human fecal metabolome profiles under 3 different dietary terms | Feces | Human | Keio University | µmol/g |