Metabolite details
Reactome pathways
- R-HSA-1430728 - Metabolism
- R-HSA-1483206 - Glycerophospholipid biosynthesis
- R-HSA-1483213 - Synthesis of PE
- R-HSA-1483257 - Phospholipid metabolism
- R-HSA-428157 - Sphingolipid metabolism
- R-HSA-556833 - Metabolism of lipids
- R-HSA-9845614 - Sphingolipid catabolism
Observed in studies
- Biological effect of chronic mistranslation in mammalian cells
- Sex-Differences in Colon Cancer Metabolism Reveal A Novel Subphenotype
- Metabolome analysis via an HPLC-ESI-MS-based experimental and computational pipeline for chronic nephron toxicity profiling
- Effect of L-carnitine administration on lipid and metabolite content in sheep infraspinatus muscle after tendon release
- Metabolomic Profile of Diet-Induced Obesity Mice in Response to Human and Small Humanin-like Peptide 2 Treatment
- Four layer multi-omics reveals molecular responses to aneuploidy in <i>Leishmania</i>
- Pb Stress and Ectomycorrhizas: Strong Protective Proteomic Responses in Poplar Roots Inoculated with <i>Paxillus involutus</i> Isolate and Characterized by Low Root Colonization Intensity.
- The impact of slyA on cell metabolism of Salmonella Typhimurium: a joint study of transcriptomics and
- The response of Chlamydomonas reinhardtii to nitrogen deprivation: a systems biology analysis
- Human age-declined saliva metabolic markers determined by LC-MS
- Metabolic Dynamics of In Vitro CD8+ T Cell Activation.
- Metabolomics identifies the intersection of phosphoethanolamine with menaquinone- triggered apoptosis in an in vitro model of leukemia
- Metabolomic profiling reveals the effects of early-life lactoferrin intervention on protein synthesis, energy production and antioxidative capacity in the liver of suckling piglets
- Bioplatforms Australia: Antibiotic Resistant Sepsis Pathogens Framework Initiative (Streptococcus pneumoniae assays)
- Bioplatforms Australia: Antibiotic Resistant Sepsis Pathogens Framework Initiative (Streptococcus pyogenes assays)
- Metabolic Dynamics in <i>Escherichia coli</i>-Based Cell-Free Systems
- Fat Deposition in the Muscle of Female and Male Yak and the Correlation of Yak Meat Quality with Fat
- Host autophagy mediates organ wasting and nutrient mobilization for tumor growth.
- Metabolic characterization of the natural progression of chronic hepatitis B (Biogenic amine and Acyl-carnitine assays).
- Dissecting Metabolism of Leaf Nodules in <i>Ardisia crenata</i> and <i>Psychotria punctata</i>.
- Changes and correlations of intestinal flora and liver metabolite profiles in mice with gallstones
- Anti-anemia drug FG4592 retards the AKI to CKD transition by improving vascular regeneration and anti-oxidative capability (day 21)
- Anti-anemia drug FG4592 retards the AKI to CKD transition by improving vascular regeneration and anti-oxidative capability (day 10)
- Jasmonate-mediated stomatal closure under elevated CO2 revealed by time-resolved metabolomics
- Chronic sleep loss sensitizes Drosophila melanogaster to nitrogen stress
- Analysis of Growth Phases of Enterotoxigenic Escherichia coli Reveals a Distinct Transition Phase before Entry into Early Stationary Phase with Shifts in Tryptophan, Fucose, and Putrescine Metabolism and Degradation of Neurotransmitter Precursors
- Metabolic plasticity confers increased resilience to climate variability in temperate compared to tropical lizards
- Gut microbiome drives individual memory variation in bumblebees
- Evaluation of algorithms for multiple alignment of GCxGC-MS data
- Exercise-generated β-aminoisobutyric acid (BAIBA) reduces cardiomyocytes metabolic stress and apoptosis caused by mitochondrial dysfunction through the miR-208b/AMPK pathway
- Metabolic profilings of rat INS-1 β-cells under changing levels of essential amino acids
- Auricularia auricula polysaccharides reduce obesity in mice through gut commensal Papillibacter cinnamivorans
- Limited nutrient availability in the tumor microenvironment renders pancreatic tumors sensitive to allosteric IDH1 inhibitors
- Intergenerational Association of Gut Microbiota and Metabolism between Perinatal Folic Acid Metabolism and Neural Tube Defects (Feces metabolomics)
- Intergenerational Association of Gut Microbiota and Metabolism between Perinatal Folic Acid Metabolism and Neural Tube Defects (Brain tissue metabolomics)
- PKM2 methylation by CARM1 activates aerobic glycolysis to promote tumorigenesis.
- Bile acid is a significant host factor shaping the gut microbiome of diet induced obese mice (untargeted metabolome profile assay)
- Flow cytometry has a significant impact on the cellular metabolome (GC-MS assay)
- Transcriptomics and metabolomics analysis reveal the anti-oxidation and immune boosting effects of mulberry leaves in growing mutton sheep
- Extracellular-acidosis restricts one-carbon metabolism and preserves T cell stemness
- TGF-β uncouples glycolysis and inflammation in macrophages and controls the survival during sepsis
- Arginine starvation kills tumor cells through aspartate exhaustion and mitochondrial dysfunction
- Disturbed Microbiota-Metabolites-Immune Interaction Network is Associated with Olfactory Dysfunction in Patients with Chronic Rhinosinusitis
- Metabolic effects of an aspartate aminotransferase-inhibitor on two T-cell lines
- Integrated multi-omics analysis of adverse cardiac remodeling and metabolic inflexibility upon ErbB2 and ERRα deficiency.
- Inhibition of glycolysis and mitochondrial respiration promotes radiosensitisation of neuroblastoma and glioma cells
- Searching for Drug Synergy Against Cancer Through Polyamine Metabolism Impairment: Insight Into the Metabolic Effect of Indomethacin on Lung Cancer Cells.
- Metabolic alterations in pea leaves during arbuscular mycorrhiza development.
Observed in differential profiles
- rps2_wildtype_vs_rps2_A226Y
- mennormal_vs_menLCCstage1
- Control_1_day_vs_High_14_day
- Control_1_day_vs_High_14_day
- Control_16.6_months_vs_Treatment_16.6_months
- Water_vs_HNG
- Water_vs_HNG
- Water_vs_HNG
- Water_vs_HNG
- Nepalese_BPK173_vs_Nepalese_BPK178
- NM-control_vs_NM-Pb
- slyA_vs_wild_type
- 0h_vs_24h
- Old_vs_Young
- G3_Experimental_Sample_0h_vs_G11_Experimental_Sample_96h
- G1_Jurkat_Negative_Control_0h_vs_G7_Jurkat_Menaquinone_72h
- Control_Day_8_vs_Lactoferrin_Day_8
- G1_Pooled_Sera_Blood_4559_vs_G2_RPMI_Glucose_Blood_4559
- G1_RPMI_modified_Blood_M1T1_5448_vs_G2_Pooled_sera_Blood_M1T1_5448
- G1_Exp1_0_hours_vs_G2_Exp1_6_hours
- Male_vs_Female
- G1_Frt_Ctrl_Day_6_vs_G3_Rasv12_Scrib_Day_6
- Control_vs_Immune_Tolerant
- Control_vs_Immune_Tolerant
- Control_vs_Immune_Tolerant
- Ardisia_crenata_Stage_I_lamina_vs_nodule
- Control_vs_Lithogenic_Diet
- Sham_vs_UIR
- Sham_vs_UIR
- 400ppm_0min_vs_800ppm_60min
- Iso31_Control_vs_Fumin_Homozygous_Sleep_Mutants
- E1777_Intracellular_MidLog_vs_E1777_Intracellular_EarlyStationary
- T_septentrionalis_cold_vs_T_septentrionalis_warm
- Hindgut_Control_vs_Lactobacillus_apis
- Hindgut_Control_vs_Lactobacillus_apis
- CC406_t2_vs_Stm6Glc4_t2
- Sham_vs_Heart_Failure_Sedentary
- G1_Control_vs_G2_Arginine_Addition
- Basal_vs_High_Fat
- Wild_Type_vs_Gene_Knockout
- Normal_vs_Neural_Tube_Defect
- Normal_vs_Neural_Tube_Defect
- MCF-7_WT_vs_MCF-7_PKM2_KO
- Normal_Diet_vs_High-fat_Diet
- Normal_Diet_vs_High-fat_Diet
- Normal_Diet_vs_High-fat_Diet
- Ctrl_vs_Ab
- Control_vs_Fermented_Mulberry_Leaves
- Control_vs_Lactic_Acid
- Control_vs_Lactic_Acid
- Control_vs_TGF-beta_Treatment
- Arginine_Replenished_Ctrl_vs_Arginine_Starved_48h
- Normal_vs_Abnormal
- JURKAT_Control_vs_JURKAT_Treatment
- WT_vs_ErbB2_KI
- G1_Untreated_Control_vs_G2_2DG
- A549_0uM_vs_A549_1uM
- 21d_Control_vs_21d_AM