List of Studies ( Metabolite:dTDP)
| Study_id | Analysis_id | Study_title | Source | Species | Disease | Institute | Analysis Type |
|---|---|---|---|---|---|---|---|
| ST003642 | AN005981 | Hexosamine Biosynthesis Disruption Impairs GPI Production and Arrests Plasmodium falciparum Growth at Schizont Stages | Cultured cells | Plasmodium falciparum | Malaria | Pennsylvania State University | LC-MS |
| ST003566 | AN006190 | Unraveling cysteine deficiency-associated rapid weight loss | Food | Mouse | Obesity | NYU Grossman School of Medicine | LC-MS |
| ST003566 | AN006190 | Unraveling cysteine deficiency-associated rapid weight loss | Liver | Mouse | Obesity | NYU Grossman School of Medicine | LC-MS |
| ST003566 | AN006190 | Unraveling cysteine deficiency-associated rapid weight loss | Stool | Mouse | Obesity | NYU Grossman School of Medicine | LC-MS |
| ST003566 | AN006190 | Unraveling cysteine deficiency-associated rapid weight loss | Urine | Mouse | Obesity | NYU Grossman School of Medicine | LC-MS |
| ST003565 | AN005858 | Metaboloomics analysis of the antimalarial compound WEHI-1888504 (aka compound 59) in Plasmodium falciparum (3D7) infected red blood cells | Cultured cells | Plasmodium falciparum | Malaria | Monash University | LC-MS |
| 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 | LC-MS |
| ST003378 | AN005533 | Effects of Aldehydes on lipid metabolism in mice | Liver | Mouse | Liver disease | Feinstein Institutes for Medical Research | LC-MS |
| ST003378 | AN005533 | Effects of Aldehydes on lipid metabolism in mice | Liver | Mouse | Obesity | Feinstein Institutes for Medical Research | LC-MS |
| ST003179 | AN005222 | Property and Activity Refinement of Dihydroquinazolinone-3-carboxamides as Orally Efficacious Antimalarials that Target PfATP4 | Plasmodium cells | Plasmodium falciparum | Malaria | Monash University | LC-MS |
| 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 | LC-MS |
| ST003121 | AN005115 | Metabolomic profiling of ALG13-CDG brain organoids | Brain organoids | Human | Genetic disease | Mayo Clinic | LC-MS |
| ST003102 | AN005076 | Cellular adaptation to cancer therapy occurs by progressive state transitions along a resistance continuum | Ovarian cancer cells | Human | Cancer | NYU Langone Health | LC-MS |
| ST003053 | AN005007 | Providing insight into the mechanism of action of Cationic Lipidated Oligomers (CLOs) using metabolomics | Bacterial cells | Staphylococcus aureus | Bacterial infection | Monash University | LC-MS |
| 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 | LC-MS | |
| ST002926 | AN004799 | Multi-“omics” analysis reveals the orphan P. falciparum protein kinase PfPK8 regulates multi-gene family expression | Blood | Plasmodium falciparum | Malaria | Monash University | LC-MS |
| ST002847 | AN004665 | Targeting Pancreatic Cancer Metabolic Dependencies through Glutamine Antagonism. | Cultured cells | Mouse | Cancer | New York University | LC-MS |
| ST002830 | AN004623 | L-isoleucine in P10 STZ | Retina | Mouse | Retinopathy of prematurity | Boston Children's Hospital | LC-MS |
| ST002584 | AN004255 | Metabolomics analysis of ALDH1L1-expressing HuH7 cell lines. | Cultured cells | Human | Cancer | Tohoku Medical and Pharmaceutical University | LC-MS |
| ST002542 | AN004189 | Methionine restriction constrains lipoylation and activates mitochondria for nitrogenic synthesis of amino acids (Part 2) | Yeast cells | Yeast | ZheJiang University | LC-MS | |
| ST002499 | AN004106 | Metabolomics analysis of stress erythroid progenitors (Part 2) | Stem cells | Mouse | Inflammation | Pennsylvania State University | LC-MS |
| ST002497 | AN004101 | Postnatal hyperglycemia alters amino acid profile in retinas | Retina | Mouse | Eye disease | Boston Children's Hospital | LC-MS |
| 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 | CE-MS |
| 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 | CE-MS |
| 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 | CE-MS |
| 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 | CE-MS |
| ST002374 | AN003869 | Metabolomics analysis of WT vs. GOT1 knockout CD8+ T cells | Cultured cells | Mouse | Johns Hopkins University | LC-MS | |
| ST002212 | AN003617 | Human fecal metabolome profiles under 3 different dietary terms | Feces | Human | Keio University | LC-MS | |
| 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 | LC-MS | |
| ST002123 | AN003476 | GCN2 regulates mitochondrial OXPHOS in HSPCs under proliferation conditions. | Bone marrow | Mouse | Sun Yat-sen University | LC-MS | |
| 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 | LC-MS |
| 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 | LC-MS |
| 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 | LC-MS |
| 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 | LC-MS |
| 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 | LC-MS |
| 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 | LC-MS |
| 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 | LC-MS |
| ST002009 | AN003275 | Metabolomics analysis of stress erythroid progenitors | Stem cells | Mouse | Inflammation | Pennsylvania State University | LC-MS |
| ST001985 | AN003236 | Profiling Plasmodium falciparum parasites and human red blood cells after treatment with MMV693183 | Blood | Human | Malaria | Pennsylvania State University | LC-MS |
| ST001985 | AN003236 | Profiling Plasmodium falciparum parasites and human red blood cells after treatment with MMV693183 | Blood | Plasmodium falciparum | Malaria | Pennsylvania State University | LC-MS |
| ST001985 | AN003236 | Profiling Plasmodium falciparum parasites and human red blood cells after treatment with MMV693183 | Cultured cells | Human | Malaria | Pennsylvania State University | LC-MS |
| ST001985 | AN003236 | Profiling Plasmodium falciparum parasites and human red blood cells after treatment with MMV693183 | Cultured cells | Plasmodium falciparum | Malaria | Pennsylvania State University | LC-MS |
| ST001860 | AN003015 | Spontaneous hydrolysis and spurious metabolic properties of α-ketoglutarate esters | Cultured cells | Human | University of British Columbia | LC-MS | |
| ST001850 | AN002997 | Unbiased LC-MS-based metabolomics analysis for both whole cell and mitochondria metabolites to gain an insight into the role of Tug1/PGC1 axis on metabolite profiles in podocytes | Epithelial cells | Mouse | University of Texas MD Anderson Cancer Center | LC-MS | |
| ST001680 | AN002738 | Metabolome of NAFLD in high fat diet mouse model | Liver | Mouse | Fatty liver disease | Weill Cornell Medicine | LC-MS |
| ST001660 | AN002711 | Plasmodium falciparum metabolomics as a result of treatment with putative acetyl-CoA synthetase inhibitors | Cultured cells | Plasmodium falciparum | Malaria | Pennsylvania State University | LC-MS |
| 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 | LC-MS |
| ST001621 | AN002656 | Untargeted metabolomics of intestinal organoids treated with fructose | Intestine | Mouse | China Pharmaceutical University | LC-MS | |
| ST001474 | AN004409 | Metabolomics of lung injury after allogeneic hematopoietic cell transplantation - Spleen ICMS | Multiple tissues | Mouse | Graft versus host disease | University of Kentucky | LC-MS |
| ST001472 | AN002448 | Metabolomics of lung injury after allogeneic hematopoietic cell transplantation - Small Intestines ICMS | SI | Mouse | Graft versus host disease | University of Kentucky | LC-MS |
| ST001470 | AN002446 | Metabolomics of lung injury after allogeneic hematopoietic cell transplantation - Lung ICMS | Mouse tissue | Mouse | Graft versus host disease | University of Kentucky | LC-MS |
| ST001453 | AN002428 | Metabolomics of lung injury after allogeneic hematopoietic cell transplantation - Liver ICMS | Liver | Human | Graft versus host disease | University of Kentucky | LC-MS |
| ST001447 | AN002418 | Metabolomics of lung injury after allogeneic hematopoietic cell transplantation - Colon ICMS | Colon | Mouse | Graft versus host disease | University of Kentucky | LC-MS |
| ST001384 | AN002309 | Plasmodium falciparum increased time in circulation underlies persistent asymptomatic infection in the dry season | Blood | Human | Malaria | Pennsylvania State University | LC-MS |
| ST001350 | AN002246 | Extraction of high-resolution Metabolomics data of the Yeast Metabolic Cycle | Yeast cells | Yeast | University of Florida | LC-MS | |
| ST001304 | AN002173 | Multi-omics analysis delineates the distinct functions of sub-cellular acetyl-CoA pools in Toxoplasma gondii | Fibroblast cells | Toxoplasma gondii | Parasitic infection | Monash University | LC-MS |
| ST001276 | AN002117 | Development and Characterisation of a Novel Class of Aroyl Guanidine Containing Anti-Trypanosomal Compounds | Cultured cells | Trypanosoma brucei | Sleeping sickness | Monash University | LC-MS |
| 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 | LC-MS |
| ST001232 | AN002050 | Combining stage - specificity and metabolomic profiling to advance drug discovery for malaria | Cultured cells | Plasmodium falciparum | Malaria | Pennsylvania State University | LC-MS |
| ST001218 | AN002031 | Wild type versus TRACK Mice on regular chow and Vitamin A deprived diet | Kidney | Mouse | Cancer | Weill Cornell Medicine | LC-MS |
| ST001188 | AN001980 | P. falciparum infected erythrocytes | Cultured cells | Plasmodium falciparum | Malaria | University of Melbourne | LC-MS |
| ST001170 | AN001935 | Timecourse on MCF-7 cells treated with different concentration of doxorubicin | Cultured cells | Human | China Pharmaceutical University | LC-MS | |
| ST001167 | AN001930 | Comprehensive Profiling by Non-targeted Stable Isotope Tracing Capillary Electrophoresis-Mass Spectrometry | Cultured cells | Human | Cancer | Dalian Institute Of Chemical Physics | LC-MS |
| 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 | LC-MS |
| ST001074 | AN001756 | Open source discovery of starting points for next generation chemoprotective antimalarial drugs (Biofocus 1) | Parasite | Human | Pennsylvania State University | LC-MS | |
| 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 | LC-MS |
| ST000441 | AN000692 | Metabolomic Profiling of the Malaria Box Reveals Antimalarial Target Pathways | Plasmodium cells | Plasmodium falciparum | Malaria | Pennsylvania State University | LC-MS |
| ST000384 | AN000619 | Metabolomic profiles in P. gingivalis cells treated with pABA | Bacterial cells | Porphyromonas | Osaka University | LC-MS | |
| 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 | LC-MS | |
| ST000121 | AN000203 | Impact of anesthesia and euthanasia on metabolomics of mammalian tissues: studies in a C57BL/6J mouse model | Blood | Mouse | University of Michigan | LC-MS | |
| ST000121 | AN000203 | Impact of anesthesia and euthanasia on metabolomics of mammalian tissues: studies in a C57BL/6J mouse model | Heart | Mouse | University of Michigan | LC-MS | |
| ST000121 | AN000203 | Impact of anesthesia and euthanasia on metabolomics of mammalian tissues: studies in a C57BL/6J mouse model | Liver | Mouse | University of Michigan | LC-MS | |
| ST000121 | AN000203 | Impact of anesthesia and euthanasia on metabolomics of mammalian tissues: studies in a C57BL/6J mouse model | Muscle | Mouse | University of Michigan | LC-MS |
