List of Studies ( Metabolite:NADP)
Study_id | Analysis_id | Study_title | Source | Species | Disease | Institute | Units(range) |
---|---|---|---|---|---|---|---|
ST000176 | AN000271 | cell and liver metabolomics | Liver | Mouse | University of Michigan | ||
ST002497 | AN004101 | Postnatal hyperglycemia alters amino acid profile in retinas | Retina | Mouse | Eye disease | Boston Children's Hospital | Absolute Intensity |
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 | Diabetes | University of Sydney | abundance |
ST003252 | AN005328 | Metabolomics studies on mouse cardiac samples on a Western diet | Heart | Mouse | Hyperglycemia | University of Sydney | abundance |
ST003252 | AN005328 | Metabolomics studies on mouse cardiac samples on a Western diet | Heart | Mouse | Hypertension | University of Sydney | abundance |
ST003252 | AN005328 | Metabolomics studies on mouse cardiac samples on a Western diet | Heart | Mouse | Obesity | University of Sydney | abundance |
ST003252 | AN005329 | Metabolomics studies on mouse cardiac samples on a Western diet | Heart | Mouse | Diabetes | University of Sydney | abundance |
ST003252 | AN005329 | Metabolomics studies on mouse cardiac samples on a Western diet | Heart | Mouse | Hyperglycemia | University of Sydney | abundance |
ST003252 | AN005329 | Metabolomics studies on mouse cardiac samples on a Western diet | Heart | Mouse | Hypertension | University of Sydney | abundance |
ST003252 | AN005329 | Metabolomics studies on mouse cardiac samples on a Western diet | Heart | Mouse | Obesity | University of Sydney | abundance |
ST003253 | AN005331 | Metabolomics studies on mouse liver samples on a Western diet | Liver | Mouse | Diabetes | University of Sydney | abundance |
ST003253 | AN005331 | Metabolomics studies on mouse liver samples on a Western diet | Liver | Mouse | Hyperglycemia | University of Sydney | abundance |
ST003253 | AN005331 | Metabolomics studies on mouse liver samples on a Western diet | Liver | Mouse | Hypertension | University of Sydney | abundance |
ST003253 | AN005331 | Metabolomics studies on mouse liver samples on a Western diet | Liver | Mouse | Obesity | University of Sydney | abundance |
ST003253 | AN005332 | Metabolomics studies on mouse liver samples on a Western diet | Liver | Mouse | Diabetes | University of Sydney | abundance |
ST003253 | AN005332 | Metabolomics studies on mouse liver samples on a Western diet | Liver | Mouse | Hyperglycemia | University of Sydney | abundance |
ST003253 | AN005332 | Metabolomics studies on mouse liver samples on a Western diet | Liver | Mouse | Hypertension | University of Sydney | abundance |
ST003253 | AN005332 | Metabolomics studies on mouse liver samples on a Western diet | Liver | Mouse | Obesity | University of Sydney | abundance |
ST001142 | AN001876 | Cancer Cell Line Encyclopedia Metabolomics | Cultured cells | Human | Cancer | Broad Institute of MIT and Harvard | Abundance |
ST001680 | AN002738 | Metabolome of NAFLD in high fat diet mouse model | Liver | Mouse | Fatty liver disease | Weill Cornell Medicine | Abundance |
ST002863 | AN004695 | Metabolic profiling and glucose tracing in naive and Enzalutamide-treated 16D prostate cancer cells | Prostate cancer cells | Human | Cancer | University of California, Los Angeles | 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 Children's 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 | |
ST001986 | AN003237 | Fbxo7 promotes Cdk6 activity to inhibit PFKP and glycolysis in T cells | T-cells | Mouse | University of Cambridge | arbitrary unit | |
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 | |
ST003586 | AN005890 | Metabolomics of the murine liver | Liver | Mouse | Diabetes | Teikyo University | arbitrary unit |
ST001062 | AN001736 | Arabidopsis Nit1 knockout metabolomics | Plant | Arabidopsis thaliana | University of California, Davis | Arbitrary units | |
ST001712 | AN002787 | Metabolomics analysis of plasma from a mouse model of astrocytoma subjected to radiotherapy | Blood | Mouse | Cancer | National Cancer Institute | 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 | AN003094 | 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) |
ST003107 | AN005086 | Characterization of metabolic changes upon FGFR inhibition in ICC13-7 Xenograft | Cultured cells | Mouse | Cancer | Massachusetts General Hospital | area analyzed by Compound Discoverer (counts x seconds) |
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 | |
ST000903 | AN001469 | Pharmacometabolomic analysis of rat hippocampus and plasma in response to chronic stress and albiflorin treament | Blood | Rat | Stress | Beijing Wonner Biotech. Ltd. Co. | Area under curve |
ST001305 | AN002174 | Integrated Metabolomics and Transcriptomics Suggest the Global Metabolic Response to 2-Aminoacrylate Stress in Salmonella enterica | Bacterial cells | Salmonella | Salmonella | University of Georgia | Area under curve |
ST001174 | AN001949 | Role of ClpCP in respiratory and fermentative growth | Bacterial cells | Staphylococcus aureus | Montana State University | Attomoles/CFU | |
ST002708 | AN004390 | Levels of central carbon metabolites in choroid plexus as part of natural diurnal variation | Brain | Mouse | Circadian Rhythm Disorder | Boston Children's Hospital | 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. |
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 |
ST002123 | AN003476 | GCN2 regulates mitochondrial OXPHOS in HSPCs under proliferation conditions. | Bone marrow | Mouse | Sun Yat-sen 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 | |
ST002457 | AN004009 | Mouse kidney metabolomics (Whole kidney) | Kidney | Mouse | Chronic kidney disease | Hadassah Medical Center | concentration |
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 |
ST000043 | AN000070 | MDA-MB-231 cells and p38 gamma knockdown | Cells | Human | University of Michigan | Counts | |
ST000044 | AN000068 | Pilot experiment looking for the existence of certain molecules in pancreatic cancer cells | Pancreas | Human | Cancer | University of Michigan | Counts |
ST000044 | AN000069 | Pilot experiment looking for the existence of certain molecules in pancreatic cancer cells | Pancreas | Human | Cancer | University of Michigan | Counts |
ST000105 | AN000174 | SCOR Metabolomics | Blood | Human | University of Michigan | Counts | |
ST000106 | AN000176 | IWMS Study 1:Weight comparison of obese and lean patients | Blood | Human | Obesity | University of Michigan | Counts |
ST000718 | AN001123 | Targeted Metabolomics in Pediatric US Population Exposed to Low-Level Heavy Metals | Cultured cells | Human | Environmental exposure | University of Michigan | Counts |
ST002747 | AN004454 | Evolutionary genomics identifies host-directed therapeutics to treat intracellular bacterial infections | Cultured cells | Human | CZ Biohub | counts, height | |
ST002747 | AN004454 | Evolutionary genomics identifies host-directed therapeutics to treat intracellular bacterial infections | Cultured cells | Rickettsia parkeri | CZ Biohub | counts, height | |
ST002747 | AN004455 | Evolutionary genomics identifies host-directed therapeutics to treat intracellular bacterial infections | Cultured cells | Human | CZ Biohub | counts, height | |
ST002747 | AN004455 | Evolutionary genomics identifies host-directed therapeutics to treat intracellular bacterial infections | Cultured cells | Rickettsia parkeri | CZ Biohub | counts, height | |
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 |
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) |
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) |
ST003435 | AN005643 | Metabolomics analysis of zebrafish embryos treated with rotenone, Fasnall, TVB-2640, and GSK2194069 | Media | Zebrafish | Cancer | Wistar Institute | Counts per second (cps) |
ST003436 | AN005645 | Pharmacokinetics of Fasnall in NSG mice | Blood | Mouse | Cancer | Wistar Institute | Counts per second (cps) |
ST003436 | AN005645 | Pharmacokinetics of Fasnall in NSG mice | Brain | Mouse | Cancer | Wistar Institute | Counts per second (cps) |
ST003436 | AN005645 | Pharmacokinetics of Fasnall in NSG mice | Heart | Mouse | Cancer | Wistar Institute | Counts per second (cps) |
ST003436 | AN005645 | Pharmacokinetics of Fasnall in NSG mice | Liver | 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 | Staphylococcus 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 |
ST001178 | AN001955 | Metabolomic analysis of C2C12 myoblasts induced by the transcriptional factor FOXO1 | Muscle | Mouse | Kyoto Prefectural University | fold | |
ST001179 | AN001957 | Metabolomic analysis of skeletal muscle in young and aged mice | Muscle | Mouse | Sarcopenia | Kyoto Prefectural University | fold |
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 | |
ST003291 | AN005390 | Atopic dermatitis and STAT3 double null mutant skin biopsies during healing. | Skin | Human | Eczema | National Institutes of Health | Intensity |
ST001188 | AN001980 | P. falciparum infected erythrocytes | Cultured cells | Plasmodium falciparum | Malaria | University of Melbourne | ion count |
ST002962 | AN004863 | LC/MS detection for NADPH and NADP+ levels in KRAS-driven lung tumors with LKB1 or p53 deficiency, comparing cases with G6PD wild-type and G6PD knockout | Lung Tumors | Mouse | Cancer | Rutgers Cancer Institute of New Jersey | Ion count |
ST003623 | AN005953 | NRF2 supports non-small cell lung cancer growth independently of CBP/p300-enhanced glutathione synthesis: Global metabolomics analysis on A549 cells at different NRF2 status (Part 1 of 3) | Cultured cells | Human | Cancer | Genentech Inc. | Ion Count |
ST001860 | AN003016 | Spontaneous hydrolysis and spurious metabolic properties of α-ketoglutarate esters | Cultured cells | Human | University of British Columbia | ion counts | |
ST002119 | AN003467 | Metabolomics analysis of zebrafish response to CID661578 treatment | Larvae | Zebrafish | Diabetes | North Carolina State University | ion counts |
ST002152 | AN003523 | Metabolomics analysis of mouse liver with or without SIRT5 deficiency | Liver | Mouse | North Carolina State University | ion counts | |
ST002847 | AN004665 | Targeting Pancreatic Cancer Metabolic Dependencies through Glutamine Antagonism. | Cultured cells | Mouse | Cancer | New York University | ion counts |
ST003549 | AN005833 | Metabolomics analysis of kidney, brain, liver, and plasma from Aldh7a1-/- and Aldh7a1+/+ mice. | Blood | Mouse | Metabolic Disorders | University of British Columbia | Ion counts |
ST003549 | AN005833 | Metabolomics analysis of kidney, brain, liver, and plasma from Aldh7a1-/- and Aldh7a1+/+ mice. | Tissue | Mouse | Metabolic Disorders | University of British Columbia | Ion counts |
ST003549 | AN005834 | Metabolomics analysis of kidney, brain, liver, and plasma from Aldh7a1-/- and Aldh7a1+/+ mice. | Blood | Mouse | Metabolic Disorders | University of British Columbia | Ion counts |
ST003549 | AN005834 | Metabolomics analysis of kidney, brain, liver, and plasma from Aldh7a1-/- and Aldh7a1+/+ mice. | Tissue | Mouse | Metabolic Disorders | University of British Columbia | Ion counts |
ST003551 | AN005837 | Metabolomics analysis of N-methyl-arginine-treated HEK293 control (sgTomato) and ALDH7A1-deficient (sgALDH7A1) cells. | Cultured cells | Human | University of British Columbia | Ion counts | |
ST003551 | AN005838 | Metabolomics analysis of N-methyl-arginine-treated HEK293 control (sgTomato) and ALDH7A1-deficient (sgALDH7A1) cells. | Cultured cells | Human | University of British Columbia | 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 |
ST002157 | AN003532 | Effect of long-term exposure to graphene on skin cell metabolism | Cultured cells | Human | University of Castilla-La Mancha | Log2 (fold-change) | |
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 |
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 |
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 | Shantou University Medical College | m/z |
ST002277 | AN003721 | Skin-to-blood pH shift triggers metabolome and proteome global remodelling in Staphylococcus epidermidis | Cultured cells | Staphylococcus epidermidis | Bacterial infection | ITQB NOVA | nanomoles |
ST002868 | AN004701 | Pathogenic Staphylococcus epidermidis ICE25 response to skin and blood pH | Bacterial cells | Staphylococcus epidermidis | Bacterial infection | ITQB NOVA | nanomoles |
ST003624 | AN005954 | NRF2 supports non-small cell lung cancer growth independently of CBP/p300-enhanced glutathione synthesis: Absolute Quantification of NADP+ and NADPH in A549 cells (Part 2 of 3) | Cultured cells | Human | Cancer | Genentech Inc. | ng/mL |
ST002174 | AN003562 | Identifying a tryptophan derivative in hydrogen peroxide-treated cell culture medium | Media | Abiotic | NYU Langone Health | N/L | |
ST002377 | AN003874 | Hepatic Phosphatidylcholine Catabolism Driven by PNPLA7 and PNPLA8 Supplies Endogenous Choline to Replenish the Methionine Cycle with Methyl Groups (Pnpla7-knockout) | Liver | Mouse | Tokyo Metropolitan Institute of Medical Science | nmol | |
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) | Cecum | 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) | Cecum | 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) | Cecum | 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) | Cecum | 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 Pharmaceutical Co., Ltd. | nmol/g tissue |
ST000351 | AN000570 | 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 |
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 |
ST000836 | AN001339 | Pilot Human Muscle oral glucose tolerance test (OGTT) | Muscle | Human | Obesity | 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 |
ST000337 | AN000547 | Metabolomics Approach to Allograft Assessment in Liver Transplantation | Liver | Human | Organ transplantation | Ochsner Multi-Organ Transplant Institute | nmol/mg dry powder |
ST000247 | AN000388 | Determining the metabolic profile of wildtype and nos mutant Staphylococcus aureus grown in media lacking glucose using targeted LC/MS | Bacterial cells | Staphylococcus aureus | University of Florida | nmol/mg protein | |
ST000468 | AN000731 | Enterococcus faecalis nucleotide profiles following mupirocin or decoyinine | Bacterial cells | Enterococcus faecalis | University of Florida | nmol/mg protein | |
ST000469 | AN000732 | Enterococcus faecalis nucleotide profiles - pilot | Bacterial cells | Enterococcus faecalis | University of Florida | nmol/mg protein | |
ST001350 | AN002246 | Extraction of high-resolution Metabolomics data of the Yeast Metabolic Cycle | Yeast cells | Yeast | University of Florida | nmol/mg protein | |
ST000687 | AN001060 | Nucleotide Analysis following Adenylate Kinase 4 knockdown | Human | University of Michigan | nmol/plate | ||
ST001779 | AN002888 | Untargeted Metabolomics analysis of A549 treated with 0.5 mM extracellular ATP and 10 ng/ml TGF-beta | Lung | Human | Cancer | Ohio University | normalized |
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 | Case Western Reserve University | Normalized Area |
ST000076 | AN000121 | A549 Cell Study | Lung | Human | University of Kentucky | normalized corrected peak area | |
ST002160 | AN003539 | Global metabolomics analysis of neutrophils isolated from tumor | Tumor cells | Mouse | Cancer | The Wistar Institute | Normalized MS Peak Area |
ST002467 | AN004023 | Nano-hijacked myeloid cells potentiate antitumor immunity and radiotherapy for glioblastoma | Brain | Mouse | Cancer | Northwestern University, Feinberg School of Medicine | Normalized peak area |
ST002009 | AN003275 | Metabolomics analysis of stress erythroid progenitors | Stem cells | Mouse | Inflammation | Pennsylvania State University | Normalized peak area |
ST001393 | AN002325 | Sea-ice diatom compatible solute shifts | Diatom cells | Nitzschia lecointei | University of Washington | Normalized Peak Area Per RFU | |
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 |
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 |
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 | 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 |
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 | |
ST002431 | AN003958 | MS profiling of the Long Term Evolution Experiment | Bacterial cells | E. coli | Rutgers University | peak area | |
ST002536 | AN004172 | Effectors enabling adaptation to mitochondrial complex I loss in Hürthle cell carcinoma | Thyroid | Human | Cancer | Broad Institute of MIT and Harvard | 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 | |
ST002712 | AN004395 | Ranolazine induced metabolic rewiring improves melanoma responses to targeted therapy and immunotherapy - metabolomics | Cultured cells | Human | Cancer | University of Colorado Denver | 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 |
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 | AN005188 | Loss of dihydroceramide desaturase drives neurodegeneration by disrupting endoplasmic reticulum and lipid droplet homeostasis in glial cells | CNS | Fruit fly | 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 | Fruit fly | Brain disease | Washington University in St. Louis | peak area |
ST003177 | AN005216 | A Longitudinal Study in Rheumatoid Arthritis Unveils Metabolomic Biomarkers Preceding Clinical Onset, Assessing Disease Severity, and Anticipating Treatment Response to csDMARDs | Blood | Human | Rheumatoid arthritis | West China Hospital of Sichuan University | peak area |
ST003331 | AN005457 | Increased Cholesterol Synthesis Drives Neurotoxicity in Patient Stem Cell-Derived Model of Multiple Sclerosis - cellular metabolomics | Stem cells | Human | Multiple sclerosis | University of Colorado Denver | 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 disease | Catholic University of the Sacred Heart | peak area |
ST003499 | AN005744 | Metabolic analysis of ADSL deficiency patients' EBV-LCLs. | Blood | Human | Mitochondrial disease | Catholic University of the Sacred Heart | peak area |
ST003608 | AN005929 | Global metabolomics to compare metabolic profiles of live vs heat-killed thymidine-auxotrophe E. Coli | Bacterial cells | E. coli | Bacterial infection | University of Colorado Anschutz Medical Campus | peak area |
ST003642 | AN005981 | Hexosamine Biosynthesis Disruption Impairs GPI Production and Arrests Plasmodium falciparum Growth at Schizont Stages | Cultured cells | Plasmodium falciparum | Malaria | Pennsylvania State University | peak area |
ST000009 | AN000024 | Mixed meal tolerance | Human | University of Michigan | Peak area | ||
ST000010 | AN000026 | Lung Cancer Cells 4 | Lung | Human | Cancer | 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 |
ST000879 | AN001430 | Diet, genetics and gut microbiome drive dynamic changes in plasma metabolites [plasma] | Mouse | Broad Institute of MIT and Harvard | 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 |
ST001256 | AN002085 | Metabolic landscape remodeling in dystrophic muscle through glucocorticoid steroid regimens | Muscle | Mouse | Muscular dystrophy | Northwestern 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 | Pennsylvania State University | 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 | |
ST001339 | AN002233 | Disruption of Redox Balance Enhances the Effects of BRAF-inhibitors in Melanoma | Tumor cells | Human | Cancer | Vanderbilt University | Peak area |
ST001441 | AN002407 | 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 | AN002783 | 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 |
ST002237 | AN003650 | Metabolomic analysis of brain cortex from neuronal specific Depdc5 knockout in fed and fasting state | Brain | Mouse | Northwestern University, Feinberg School of Medicine | 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 |
ST002846 | AN004664 | Apolipoprotein E suppresses hyperlipidemia-driven hematopoiesis & inflammation by controlling mitochondrial metabolism | Macrophages | Mouse | Hyperlipidemia | Northwestern 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 |
ST003265 | AN005349 | Malic Enzyme 2 maintains metabolic state and anti-tumor immunity of CD8+ T cells | T-cells | Mouse | Cancer | Peking Union Medical College | Peak area |
ST003577 | AN005873 | Multi ‘omics indicate depth-discrete partitioning of nitrogen metabolism in a toxic Planktothrix rubescens bloom in the winter water column | Water | Other | University of Tennessee | 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 | AN004705 | Atlas of fetal metabolism during mid-to-late gestation and diabetic pregnancy | Embryonic cells | Mouse | Diabetes | University of California, Los Angeles | Peak Area |
ST002852 | AN004672 | 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 | AN004715 | 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 |
ST002935 | AN004814 | Title: Myeloid cell-derived creatine in the hypoxic niche promotes glioblastoma growth | Brain | Human | Cancer | Northwestern University, Feinberg School of Medicine | 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 |
ST003166 | AN005195 | Metabolomics of Murine WT or MCJ KO CD19-BBz CD8 CAR-T cells | T-cells | Mouse | Cancer | University of Colorado School of Medicine | Peak Area |
ST003588 | AN005892 | Mitochondria complex III is essential for IL-10 secretion in macrophages independent of respiration | Macrophages | Mouse | Influenza | Northwestern University, Feinberg School of Medicine | Peak Area |
ST003588 | AN005892 | Mitochondria complex III is essential for IL-10 secretion in macrophages independent of respiration | Macrophages | Mouse | Toxic shock | Northwestern University, Feinberg School of Medicine | Peak Area |
ST002531 | AN004165 | Cellular consumption/release of polar metabolites by mPDAC cells cultured in different culture media conditions | Media | Mouse | Cancer | University of Chicago | Peak area (m/z) |
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) | |
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 |
ST001298 | AN002162 | Metabolome Profiling of Synechococcus elongatus PCC 11801 strains engineered for Succinate Production | Bacterial cells | Synechococcus elongatus | Indian Institute of Technology 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 | Worms | C. elegans | Hiroshima University | peak areas | |
ST002031 | AN003301 | Irradiation causes alterations of polyamine, purine and sulfur metabolism in red blood cells and multiple organs (Whole blood) | Blood | Mouse | University of Colorado Anschutz Medical Campus | peak area top | |
ST002036 | AN003311 | Irradiation causes alterations of polyamine, purine and sulfur metabolism in red blood cells and multiple organs (Kidney) | Kidney | Mouse | University of Colorado Anschutz Medical Campus | peak area top | |
ST002039 | AN003317 | Irradiation causes alterations of polyamine, purine and sulfur metabolism in red blood cells and multiple organs (Brain) | Brain | Mouse | University of Colorado Anschutz Medical Campus | peak area top | |
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) | |
ST002066 | AN003365 | Glutaminase inhibition impairs CD8 T cell activation in STK11/Lkb1 deficient lung cancer | Lung | Mouse | Cancer | The Walter and Eliza Hall Institute of Medical Research | peak height |
ST002412 | AN003931 | Metabolic effects of the protein kinase R | Macrophages | Mouse | Hudson Institute of Medical Research | 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 | AN000642 | Metabolomics-based elucidation of active metabolic pathways in erythrocytes and HSC-derived reticulocytes | Cells | Human | Monash Institute of Pharmaceutical Sciences | Peak height | |
ST000414 | AN000655 | Metabolomics-based screening of the Malaria Box reveals both novel and established mechanisms of action | Cells | Plasmodium falciparum | Malaria | Monash Institute of Pharmaceutical Sciences | Peak height |
ST000539 | AN000818 | Metabolomics-based elucidation of active metabolic pathways in erythrocytes and HSC-derived reticulocytes (part II) | Cells | Human | Monash University | Peak height | |
ST000546 | AN000832 | Multi-omics based identification of specific biochemical changes associated with PfKelch13-mutant artemisinin resistant Plasmodium | Cells | Plasmodium falciparum | Malaria | Monash University | Peak height |
ST001033 | AN001694 | Determination of mode of action of anti-malalrial drugs using untargeted metabolomics | Cultured cells | Plasmodium falciparum | Malaria | 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 |
ST002991 | AN004911 | Metabolomics studies on human colorectal cancer cell lines | Cultured cells | Human | Cancer | The University of Newcastle | peak intensity |
ST003112 | AN005111 | Glucose Hypometabolism Prompts RAN Translation and Exacerbates C9orf72-related ALS/FTD Phenotypes | Brain | Mouse | Neurodegenerative disease | 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 disease | 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 |
ST001204 | AN002005 | Peroxide antimalarial extended treatment timecourse on trophozoite-stage P. falciparum parasites | Cultured cells | Human | Malaria | Monash University | Peak intensity |
ST001204 | AN002005 | Peroxide antimalarial extended treatment timecourse on trophozoite-stage P. falciparum parasites | Cultured cells | Plasmodium falciparum | Malaria | Monash University | Peak intensity |
ST001205 | AN002006 | Peroxide antimalarial treatment of K13-mutant and -wildtype P. falciparum parasites | Cultured cells | Human | Malaria | Monash University | Peak intensity |
ST001205 | AN002006 | Peroxide antimalarial treatment of K13-mutant and -wildtype P. falciparum parasites | Cultured cells | Plasmodium falciparum | Malaria | Monash University | Peak intensity |
ST001373 | AN002293 | Targeting Sirt2 reprograms T cell metabolism for effective immune response | Spleen | Mouse | Moffitt Cancer Center | 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 | |
ST001527 | AN002548 | Lung cancer metabolomics analysis | Tumor cells | Human | Cancer | University of Louisville | Peak intensity |
ST001547 | AN002577 | 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 | Zhejiang University | Peak intensity | |
ST002541 | AN004187 | Methionine restriction constrains lipoylation and activates mitochondria for nitrogenic synthesis of amino acids (Part 1) | Yeast cells | Yeast | Zhejiang University | Peak intensity | |
ST002542 | AN004188 | Methionine restriction constrains lipoylation and activates mitochondria for nitrogenic synthesis of amino acids (Part 2) | Yeast cells | Yeast | ZheJiang University | Peak intensity | |
ST002542 | AN004189 | Methionine restriction constrains lipoylation and activates mitochondria for nitrogenic synthesis of amino acids (Part 2) | Yeast cells | Yeast | 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 |
ST002936 | AN004815 | O-GlcNAcase activity maintains stress granules for proximity-enhanced ATP production to ensure recovery from stress (Part 2) | Cultured cells | Human | Zhejiang University | Peak intensity | |
ST002936 | AN004816 | O-GlcNAcase activity maintains stress granules for proximity-enhanced ATP production to ensure recovery from stress (Part 2) | Cultured cells | Human | Zhejiang University | Peak intensity | |
ST003145 | AN005161 | Muscle-type specific stress responses explain the onset of external ophthalmoplegia in mitochondrial disease | Muscle | Mouse | Mitochondrial disease | University of Helsinki | Peak intensity |
ST003174 | AN005209 | O-GlcNAcase activity maintains stress granules for proximity-enhanced ATP production to ensure recovery from stress (Part 3) | Cultured cells | Human | Zhejiang University | Peak intensity | |
ST003174 | AN005210 | O-GlcNAcase activity maintains stress granules for proximity-enhanced ATP production to ensure recovery from stress (Part 3) | Cultured cells | Human | Zhejiang University | Peak intensity | |
ST002068 | AN003370 | Mutant CHCHD10 causes an extensive metabolic rewiring that precedes OXPHOS dysfunction in a murine model of mitochondrial cardiomyopathy | Heart | Mouse | Heart disease | Weill Cornell Medicine | Peak Intensity |
ST002068 | AN003371 | Mutant CHCHD10 causes an extensive metabolic rewiring that precedes OXPHOS dysfunction in a murine model of mitochondrial cardiomyopathy | Heart | Mouse | Heart disease | Weill Cornell Medicine | 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 |
ST001135 | AN001861 | Different dose exposure of OPC-163493 on HepG2 cells (part-I) | Hep G2 cells | Human | Diabetes | Otsuka Pharmaceutical Co., Ltd. | 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 | |
ST002281 | AN003726 | Metabolite patterns between isogenic normal hiPSCs and Trisomy hiPSC | iPSC cells | Human | Down syndrome | Guangdong Provincial People's Hospital | 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 |
ST000287 | AN000456 | Energetics in dystrophic muscle | Muscle | Mouse | Muscular dystrophy | University of Florida | pmol/mg dry powder |
ST002595 | AN004267 | MoTrPAC: Endurance exercise training study in young adult rats, Rat Gastrocnemius Powder - Targeted Nucleotides | Gastrocnemius | Rat | Duke University | pmol/mg of tissue | |
ST002601 | AN004273 | MoTrPAC: Endurance exercise training study in young adult rats, Rat Heart Powder - Targeted Nucleotides | Heart | Rat | Duke University | pmol/mg of tissue | |
ST002615 | AN004287 | MoTrPAC: Endurance exercise training study in young adult rats, Rat Liver Powder - Targeted Nucleotides | Liver | Rat | Duke University | pmol/mg of tissue | |
ST002625 | AN004297 | MoTrPAC: Endurance exercise training study in young adult rats, Rat White Adipose Powder - Targeted Nucleotides | 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 | |
ST000176 | AN000270 | cell and liver metabolomics | Liver | Mouse | University of Michigan | pmol/mg protein | |
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 |
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 | |
ST000373 | AN000607 | Measure change in metabolites based on diet and feeding status (part II) | Brain | Fruit fly | University of Michigan | pmol/ug protein | |
ST000832 | AN001838 | Rat Retinal Detachment Metabolomics Timecourse | Eye tissue | Rat | 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 | |
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 Children's Hospital, Harvard Medical School | 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 |
ST002084 | AN003401 | A genome-scale gain-of-function CRISPR screen in CD8 T cells identifies proline metabolism as a means to enhance CAR-T therapy(Part 2) | Cultured cells | Human | Cancer | Yale University | ppm |
ST003080 | AN005038 | Metabolome changes in embryonic CSF (Part 2) | CSF | Mouse | Autism | 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) | |
ST003495 | AN005736 | Hepatocyte Period 1 dictates oxidative substrate selection independent of the core circadian clock | Liver | Mouse | Washington University in St. Louis | Raw Area | |
ST003101 | AN005073 | Parallel pheromonal, metabolite, and lipid analyses reveal patterns associated with early life transitions and ovary activation in honey bee (Apis mellifera) queens | Bee heads | Honey bee | Life Sciences Institute, The University of British Columbia | Rel 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 |
ST000384 | AN000619 | Metabolomic profiles in P. gingivalis cells treated with pABA | Bacterial cells | Porphyromonas | Osaka University | Relative Area | |
ST001668 | AN002721 | D-Allulose effects on hepatic metabolomics profile in rodents | Liver | Rat | Matsutani Chemical Industry Co., Ltd. | Relative Area | |
ST001684 | AN002750 | An overexpression of lipoprotein lipase leads to an alteration in the skeletal muscle metabolome in transgenic rabbits | Muscle | Rabbit | Saga University | Relative Area | |
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 | AN003446 | 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 |
ST002309 | AN003772 | Targeting malaria parasites with novel derivatives of azithromycin | Blood | Plasmodium falciparum | Malaria | Monash University | 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 | Relative intensity after normalization |
ST001175 | AN001950 | Multi-omics analysis demonstrates unique mode of action of a potent new antimalarial compound, JPC-3210, against Plasmodium falciparum | Plasmodium cells | Plasmodium falciparum | Malaria | Monash University | Signal Intensity |
ST001304 | AN002172 | 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 |
ST001315 | AN002190 | Retargeting azithromycin-like compounds as antimalarials with dual modality | Blood | Plasmodium falciparum | Malaria | 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 | |
ST002231 | AN003640 | 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 |
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 |
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 | University of Michigan | 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 |
ST000833 | AN001841 | Influence of murine norovirus on cell metabolism | Cultured cells | Mouse | University of Michigan | uM | |
ST003516 | AN005773 | Macrophages are activated towards phagocytic Lymphoma Cell Clearance by Pentose Phosphate Pathway Inhibition | Cultured cells | Mouse | Cancer | Universidad CEU San Pablo | 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) | |
ST001614 | AN002649 | NMR metabolomics analysis of ricin-induced and fasting hypoglycemia (part-I) | Liver | Mouse | Hypoglycemia | Montana State University | uM/mg liver tissue |
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 |
ST000478 | AN000744 | NMR based Metabolomics Analysis of Liver from C57BL/6 Mouse Exposed to Ionizing Radiation | Liver | Mouse | Radiation exposure | Pacific Northwest National Laboratory | umoles/mg |
ST000479 | AN000745 | NMR based quantitative metabolomics studies of heart and lung from mouse exposed to whole body high dose gamma and proton radiation | Muscle | Mouse | Radiation exposure | Pacific Northwest National Laboratory | umoles/mg |
ST000480 | AN000746 | NMR based quantitative metabolomics studies of heart and lung from mouse exposed to whole body high dose gamma and proton radiation (part II) | Lung | Mouse | Radiation exposure | Pacific Northwest National Laboratory | umoles/mg |
ST000500 | AN000769 | Metabolomics Analysis of Kidney from C57BL/6 Mouse Exposed to Ionizing Radiation | Kidney | Mouse | Radiation exposure | Pacific Northwest National Laboratory | umoles/mg |
ST003647 | AN005990 | Targeted mass spec-based metabolomic and clinical analyte analyses of liver and plasma samples from rats with and without hepatic knockdown of ChREBP expression. | Liver | Mouse | Duke University | µM |